| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by journal name.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1801 | 6 | 7 | 650 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(3):473-476 BOLTON P; RUTTER M; BUTLER L; SUMMERS D FEMALES WITH AUTISM AND THE FRAGILE-X | 7 | 11 |
| 1802 | 0 | 1 | 651 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(4):643-643 LACHIEWICZ AM FRAGILE-X SYNDROME - A HANDBOOK FOR FAMILIES AND EDUCATORS - FINUCANE,B | 0 | 0 |
| 1803 | 6 | 28 | 872 1991 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 21(4):503-516 HODAPP RM; DYKENS EM; ORT SI; ZELINSKY DG; LECKMAN JF CHANGING PATTERNS OF INTELLECTUAL STRENGTHS AND WEAKNESSES IN MALES WITH FRAGILE-X SYNDROME | 5 | 16 |
| 1804 | 7 | 26 | 1123 1993 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 23(1):135-145 DYKENS EM; HODAPP RM; ORT SI; LECKMAN JF TRAJECTORY OF ADAPTIVE-BEHAVIOR IN MALES WITH FRAGILE X-SYNDROME | 27 | 37 |
| 1805 | 23 | 40 | 1124 1993 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 23(1):201-209 HASHIMOTO O; SHIMIZU Y; KAWASAKI Y LOW-FREQUENCY OF THE FRAGILE-X SYNDROME AMONG JAPANESE AUTISTIC SUBJECTS | 3 | 8 |
| 1806 | 10 | 23 | 1254 1994 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 24(4):473-485 MAZZOCCO MMM; PENNINGTON BF; HAGERMAN RJ SOCIAL COGNITION SKILLS AMONG FEMALES WITH FRAGILE-X | 9 | 12 |
| 1807 | 5 | 24 | 1400 1995 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 25(6):655-662 Lenti C; Peruzzi C; Bianchini E The association between autism and fragile X syndrome: A case report | 0 | 1 |
| 1808 | 6 | 29 | 1545 1996 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 26(3):287-301 Dykens E; Ort S; Cohen I; Finucane B; Spiridigliozzi G; et al. Trajectories and profiles of adaptive behavior in males with fragile X syndrome: Multicenter studies | 19 | 23 |
| 1809 | 24 | 61 | 1671 1997 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 27(4):415-435 Mazzocco MMM; Kates WR; Baumgardner TL; Freund LS; Reiss AL Autistic behaviors among girls with fragile X syndrome | 20 | 25 |
| 1810 | 10 | 39 | 1760 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(4):321-328 Mazzocco MMM; Pulsifer M; Fiumara A; Cocuzza M; Nigro F; et al. Brief report: Autistic behaviors among children with fragile X or Rett syndrome: Implications for the classification of pervasive developmental disorder | 4 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1811 | 53 | 104 | 1761 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(5):393-405 Feinstein C; Reiss AL Autism: The point of view from fragile X studies | 18 | 45 |
| 1812 | 17 | 28 | 1762 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):499-508 Bailey DB; Mesibov GB; Hatton DD; Clark RD; Roberts JE; et al. Autistic behavior in young boys with fragile X syndrome | 31 | 40 |
| 1813 | 12 | 36 | 1763 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):509-517 Mazzocco MMM; Baumgardner T; Freund LS; Reiss AL Social functioning among girls with fragile X or Turner syndrome and their sisters | 11 | 15 |
| 1814 | 10 | 41 | 2031 2000 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 30(1):49-59 Bailey DB; Hatton DD; Mesibov G; Ament N; Skinner M Early development, temperament, and functional impairment in autism and fragile X syndrome | 16 | 19 |
| 1815 | 16 | 33 | 2163 2001 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 31(2):165-174 Bailey DB; Hatton DD; Skinner M; Mesibov G Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome | 16 | 22 |
| 1816 | 2 | 3 | 2290 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(1):60-61 Rapin I Legitimacy of comparing fragile X with autism questioned | 0 | 0 |
| 1817 | 17 | 39 | 2291 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(2):107-114 Fisch GS; Simensen RJ; Schroer RJ Longitudinal changes in cognitive and adaptive Behavior scores in children and adolescents with the fragile X mutation or autism | 2 | 3 |
| 1818 | 20 | 54 | 2436 2003 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 33(1):55-67 Lesniak-Karpiak K; Mazzocco MMM; Ross JL Behavioral assessment of social anxiety in females with Turner or fragile X syndrome | 0 | 6 |
| 1819 | 5 | 50 | 2535 2004 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 34(1):41-48 Seltzer MM; Abbeduto L; Krauss MW; Greenberg J; Swe A Comparison groups in autism family research: Down syndrome, fragile X syndrome, and schizophrenia | 0 | 2 |
| 1820 | 1 | 22 | 1401 1995 JOURNAL OF BACTERIOLOGY 177(7):1915-1917 FUTO S; SETO Y; MITSUSE S; MORI Y; SUZUKI T; et al. MOLECULAR-CLONING OF A 46-KILODALTON SURFACE-ANTIGEN (P46) GENE FROM MYCOPLASMA-HYOPNEUMONIAE - DIRECT EVIDENCE OF CGG CODON USAGE FOR ARGININE | 0 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1821 | 0 | 53 | 2292 2002 JOURNAL OF BACTERIOLOGY 184(1):177-182 Semsey S; Blaha B; Koles K; Orosz L; Papp PP Site-specific integrative elements of rhizobiophage 16-3 can integrate into proline tRNA (CGG) genes in different bacterial genera | 1 | 6 |
| 1822 | 2 | 43 | 1402 1995 JOURNAL OF BIOLOGICAL CHEMISTRY 270(39):23090-23096 CHEN FM ACID-FACILITATED SUPRAMOLECULAR ASSEMBLY OF G-QUADRUPLEXES IN D(CGG)(4) | 10 | 37 |
| 1823 | 3 | 44 | 1403 1995 JOURNAL OF BIOLOGICAL CHEMISTRY 270(45):27014-27021 KANG SM; OHSHIMA K; SHIMIZU M; AMIRHAERI S; WELLS RD PAUSING OF DNA-SYNTHESIS IN-VITRO AT SPECIFIC LOCI IN CTG AND CGG TRIPLET REPEATS FROM HUMAN HEREDITARY-DISEASE GENES | 16 | 96 |
| 1824 | 15 | 46 | 1404 1995 JOURNAL OF BIOLOGICAL CHEMISTRY 270(48):28970-28977 NADEL Y; WEISMANSHOMER P; FRY M THE FRAGILE-X SYNDROME SINGLE-STRAND D(CGG)(N) NUCLEOTIDE REPEATS READILY FOLD BACK TO FORM UNIMOLECULAR HAIRPIN STRUCTURES | 17 | 50 |
| 1825 | 8 | 43 | 1546 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(8):4327-4334 Deissler H; BehnKrappa A; Doerfler W Purification of nuclear proteins from human HeLa cells that bind specifically to the unstable tandem repeat (CGG), in the human FMR1 gene | 11 | 24 |
| 1826 | 6 | 37 | 1547 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(38):22937-22940 Wang YH; Griffith J Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion | 4 | 23 |
| 1827 | 11 | 50 | 1548 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(40):24325-24328 Godde JS; Kass SU; Hirst MC; Wolffe AP Nucleosome assembly on methylated CGG triplet repeats in the Fragile X Mental Retardation gene 1 promoter | 5 | 41 |
| 1828 | 15 | 47 | 1672 1997 JOURNAL OF BIOLOGICAL CHEMISTRY 272(27):16761-16768 Deissler H; Wilm M; Genc B; Schmitz B; Ternes T; et al. Rapid protein sequencing by tandem mass spectrometry and cDNA cloning of p20-CGGBP - A novel protein that binds to the unstable triplet repeat 5'-d(CGG)(n)-3' in the human FMR1 gene | 5 | 17 |
| 1829 | 4 | 60 | 1673 1997 JOURNAL OF BIOLOGICAL CHEMISTRY 272(27):16783-16792 Bacolla A; Gellibolian R; Shimizu M; Amirhaeri S; Kang S; et al. Flexible DNA: Genetically unstable CTG center dot CAG and CGG center dot CCG from human hereditary neuromuscular disease genes | 3 | 57 |
| 1830 | 12 | 37 | 1764 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(25):15521-15527 Brown V; Small K; Lakkis L; Feng Y; Gunter C; et al. Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein | 45 | 69 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1831 | 6 | 30 | 1765 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(27):17122-17127 Bolivar J; Guelman S; Iglesias C; Ortiz M; Valdivia MM The fragile-X-related gene FXR1 is a human autoantigen processed during apoptosis | 3 | 7 |
| 1832 | 4 | 66 | 1766 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(41):26998-27008 Parsons MA; Sinden RR; Izban MG Transcriptional properties of RNA polymerase II within triplet repeat-containing DNA from the human myotonic dystrophy and fragile X loci | 0 | 14 |
| 1833 | 1 | 38 | 1767 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(46):30466-30471 Mangel L; Ternes T; Schmitz B; Doerfler W New 5 '-(CGG)(n)-3 ' repeats in the human genome | 3 | 5 |
| 1834 | 11 | 41 | 1907 1999 JOURNAL OF BIOLOGICAL CHEMISTRY 274(18):12797-12802 Fry M; Loeb LA Human Werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)(n) | 11 | 104 |
| 1835 | 20 | 50 | 2032 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(3):2231-2238 Weisman-Shomer P; Naot Y; Fry M Tetrahelical forms of the fragile X syndrome expanded sequence d(CGG)(n) are destabilized by two heterogeneous nuclear ribonucleoprotein-related telomeric DNA-binding proteins | 7 | 10 |
| 1836 | 9 | 29 | 2033 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(9):6447-6452 Muller-Hartmann H; Deissler H; Naumann F; Schmitz B; Schroer J; et al. The human 20-kDa 5 '-(CGG)(n)-3 '-binding protein is targeted to the nucleus and affects the activity of the FMR1 promoter | 11 | 16 |
| 1837 | 27 | 59 | 2034 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(42):33134-33141 Uliel L; Weisman-Shomer P; Oren-Jazans H; Newcomb T; Loeb LA; et al. Human Ku antigen tightly binds and stabilizes a tetrahelical form of the fragile X syndrome d(CGG)(n) expanded sequence | 1 | 7 |
| 1838 | 10 | 28 | 2164 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(6):4357-4364 Kumari D; Usdin K Interaction of the transcription factors USF1, USF2, and alpha-Pal/Nrf-1 with the FMR1 promoter - Implications for Fragile X mental retardation syndrome | 15 | 23 |
| 1839 | 15 | 58 | 2165 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(19):16439-16446 Kamath-Loeb AS; Loeb LA; Johansson E; Burgers PMJ; Fry M Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)(n) trinucleotide repeat sequence | 4 | 44 |
| 1840 | 8 | 71 | 2166 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(21):18605-18613 Bacolla A; Pradhan S; Larson JE; Roberts RJ; Wells RD Recombinant human DNA (cytosine-5) methyltransferase - III. Allosteric control, reaction order, and influence of plasmid topology and triplet repeat length on methylation of the fragile X CGG center dot CCG sequence | 0 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1841 | 0 | 44 | 2293 2002 JOURNAL OF BIOLOGICAL CHEMISTRY 277(23):21041-21049 Vargason JM; Ho PS The effect of cytosine methylation on the structure and geometry of the Holliday junction - The structure of d(CCGGTACm(5)CGG) at 1.5 angstrom resolution | 0 | 9 |
| 1842 | 14 | 54 | 2294 2002 JOURNAL OF BIOLOGICAL CHEMISTRY 277(40):37804-37810 Ohashi S; Koike K; Omori A; Ichinose S; Ohara S; et al. Identification of mRNA/protein (mRNP) complexes containing Pur alpha, mStaufen, Fragile X Protein, and myosin Va and their association with rough endoplasmic reticulum equipped with a kinesin motor | 18 | 48 |
| 1843 | 30 | 56 | 2437 2003 JOURNAL OF BIOLOGICAL CHEMISTRY 278(18):15669-15678 Sung YJ; Dolzhanskaya N; Nolin SL; Brown T; Currie JR; et al. The fragile X mental retardation protein FMRP binds elongation factor 1A mRNA and negatively regulates its translation in vivo | 8 | 13 |
| 1844 | 21 | 46 | 2637 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280(6):4498-4503 Mulvihill DJ; Edamura KN; Hagerman KA; Pearson CE; Wang YH Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome | 0 | 0 |
| 1845 | 23 | 47 | 2638 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280(7):5750-5763 Garnon J; Lachance C; Di Marco S; Hel Z; Marion D; et al. Fragile X-related protein FXR1P regulates proinflammatory cytokine tumor necrosis factor expression at the post-transcriptional level | 0 | 0 |
| 1846 | 11 | 33 | 1768 1998 JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS 15(4):745-756 Chen X; Mariappan SVS; Moyzis RK; Bradbury EM; Gupta G Hairpin induced slippage and hyper-methylation of the fragile X DNA triplets | 4 | 16 |
| 1847 | 18 | 36 | 713 1990 JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME 72A(6):889-896 DAVIDS JR; HAGERMAN RJ; EILERT RE ORTHOPEDIC ASPECTS OF FRAGILE-X SYNDROME | 0 | 13 |
| 1848 | 0 | 0 | 1255 1994 JOURNAL OF CELLULAR BIOCHEMISTRY :184-184 WARREN ST OVERVIEW AND UPDATE ON FMR1 AND FRAGILE-X SYNDROME | 0 | 0 |
| 1849 | 0 | 0 | 1405 1995 JOURNAL OF CELLULAR BIOCHEMISTRY :100-100 MCMURRAY CT; GACY AM; GOELLNER G HAIRPIN STABILITY DETERMINES THE THRESHOLD AND POTENTIAL FOR NUCLEOTIDE EXPANSION ASSOCIATED WITH HUMAN NEURODEGENERATIVE DISEASE | 0 | 0 |
| 1850 | 0 | 0 | 1406 1995 JOURNAL OF CELLULAR BIOCHEMISTRY :373-373 WILLEMS PJ; BAKKER CE; REYNIERS E; VERHEIJ C; DEBOULLE K; et al. A TRANSGENIC MOUSE MODEL FOR FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1851 | 7 | 18 | 1908 1999 JOURNAL OF CHILD NEUROLOGY 14(2):108-112 Singh R; Sutherland GR; Manson J Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndrome | 1 | 1 |
| 1852 | 60 | 103 | 2536 2004 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY 45(6):1042-1053 Cornish KM; Turk J; Wilding J; Sudhalter V; Munir F; et al. Annotation: Deconstructing the attention deficit in fragile X syndrome: a developmental neuropsychological approach | 0 | 0 |
| 1853 | 3 | 13 | 604 1988 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 29(4):447-451 GILLBERG C; OHLSON VA; WAHLSTROM J; STEFFENBURG S; BLIX K MONOZYGOTIC FEMALE TWINS WITH AUTISM AND THE FRAGILE-X SYNDROME (AFRAX) | 9 | 19 |
| 1854 | 2 | 33 | 652 1989 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 30(6):845-856 COHEN IL; VIETZE PM; SUDHALTER V; JENKINS EC; BROWN WT PARENT CHILD DYADIC GAZE PATTERNS IN FRAGILE-X MALES AND IN NON-FRAGILE-X MALES WITH AUTISTIC DISORDER | 31 | 49 |
| 1855 | 0 | 1 | 714 1990 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 31(7):1165-1166 BOLTON P THE FRAGILE X-SYNDROME - DAVIES,K | 0 | 0 |
| 1856 | 49 | 76 | 997 1992 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 33(7):1127-1139 HAGERMAN RJ FRAGILE-X SYNDROME - ADVANCES AND CONTROVERSY | 3 | 7 |
| 1857 | 25 | 50 | 1125 1993 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 34(5):673-688 BAILEY A; BOLTON P; BUTLER L; LECOUTEUR A; MURPHY M; et al. PREVALENCE OF THE FRAGILE-X ANOMALY AMONGST AUTISTIC TWINS AND SINGLETONS | 11 | 50 |
| 1858 | 0 | 1 | 1407 1995 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 36(4):707-707 TURK J BEHAVIOR AND DEVELOPMENT IN FRAGILE-X SYNDROME - DYKENS,EM, HODAPP,RM, LECKMAN,JF | 0 | 0 |
| 1859 | 7 | 40 | 1769 1998 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 39(5):699-710 van Lieshout CFM; De Meyer RE; Curfs LMG; Fryns JP Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome | 4 | 16 |
| 1860 | 4 | 53 | 2295 2002 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 43(7):949-957 von Gontard A; Backes M; Laufersweiler-Plass C; Wendland C; Lehmkuhl G; et al. Psychopathology and familial stress - comparison of boys with Fragile X syndrome and Spinal Muscular Atrophy | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1861 | 0 | 0 | 715 1990 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 12(1):69-69 KAUFMANN PM; LECKMAN JF; ORT SI DELAYED-RESPONSE PERFORMANCE IN MALES WITH FRAGILE-X SYNDROME | 3 | 5 |
| 1862 | 23 | 37 | 1408 1995 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 17(4):518-528 HINTON VJ; HALPERIN JM; DOBKIN CS; DING XH; BROWN WT; et al. COGNITIVE AND MOLECULAR ASPECTS OF FRAGILE-X | 5 | 9 |
| 1863 | 22 | 57 | 2537 2004 JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 89(9):4569-4574 Welt CK; Smith PC; Taylor AE Evidence of early ovarian aging in fragile X premutation carriers | 0 | 0 |
| 1864 | 21 | 51 | 1674 1997 JOURNAL OF CLINICAL INVESTIGATION 100(2):331-338 Jakala P; Hanninen T; Ryynanen M; Laakso M; Partanen K; et al. Fragile-X: Neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes | 13 | 21 |
| 1865 | 50 | 75 | 1770 1998 JOURNAL OF CLINICAL LIGAND ASSAY 21(4):424-431 Feldman GL; Monaghan KG Fragile X syndrome: A review of the molecular and clinical features | 0 | 0 |
| 1866 | 0 | 30 | 2538 2004 JOURNAL OF CLINICAL MICROBIOLOGY 42(8):3538-3548 Otsuka Y; Parniewski P; Zwolska Z; Kai M; Fujino T; et al. Characterization of a trinucleotide repeat sequence (CGG)(5) and potential use in restriction fragment length polymorphism typing of Mycobacterium tuberculosis | 0 | 1 |
| 1867 | 3 | 8 | 2639 2005 JOURNAL OF CLINICAL NEUROSCIENCE 12(1):42-43 Storey E; Billimoria P Increased T-2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X premutation syndrome | 0 | 0 |
| 1868 | 4 | 15 | 873 1991 JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY 11(6):398-399 COHEN IL; TSIOURIS JA; PFADT A EFFECTS OF LONG-ACTING PROPRANOLOL ON AGONISTIC AND STEREOTYPED BEHAVIORS IN A MAN WITH PERVASIVE DEVELOPMENTAL DISORDER AND FRAGILE-X SYNDROME - A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY | 2 | 5 |
| 1869 | 0 | 0 | 2035 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :57-57 Merin NM; Menon V; White CD; Glover GH; Reiss AL Gaze processing deficits in fragile X syndrome investigated using fMRI | 0 | 0 |
| 1870 | 0 | 0 | 2036 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :98-98 White CD; Menon V; Eliez S; Reiss AL An fMRI study of brain activation in Fragile X Syndrome during a go-nogo task | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1871 | 0 | 0 | 2037 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :146-146 Kwon H; Menon V; Eliez S; Dyer-Friedman J; Glover GH; et al. Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavior and FMR-1 protein expression | 0 | 0 |
| 1872 | 0 | 0 | 2296 2002 JOURNAL OF COGNITIVE NEUROSCIENCE :50-51 Scerif G; Wilding J; Cornish K; Driver J; Humphreys K; et al. Executive control in visual search for multiple targets in toddlers with Fragile X Syndrome | 0 | 0 |
| 1873 | 8 | 61 | 2297 2002 JOURNAL OF COGNITIVE NEUROSCIENCE 14(2):160-171 Tamm L; Menon V; Johnston CK; Hessl DR; Reiss AL fMRI study of cognitive interference processing in females with fragile X syndrome | 6 | 10 |
| 1874 | 0 | 14 | 2167 2001 JOURNAL OF CRYSTAL GROWTH 226(1):101-106 Jung IH; Yoshikawa A; Lebbou K; Fukuda T; Auh KH Crystal growth by micro-pulling-down of Ca3Ga2Ge4O14 (CGG) type-Sr3Nb1-xGa3 (+) (5/3)xSi2O14 compounds | 0 | 8 |
| 1875 | 0 | 0 | 2168 2001 JOURNAL OF DENTAL RESEARCH 80(4):1133-1133 Sabbagh A Clinical and panoramic radiographic considerations of oral conditions in Fragile X Syndrome (Martin-Bell Syndrome) | 0 | 0 |
| 1876 | 13 | 68 | 144 1983 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 4(2):122-130 HAGERMAN RJ; MCBOGG P; HAGERMAN PJ THE FRAGILE-X SYNDROME - HISTORY, DIAGNOSIS, AND TREATMENT | 14 | 18 |
| 1877 | 7 | 20 | 145 1983 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 4(3):151-158 LEVITAS A; HAGERMAN RJ; BRADEN M; RIMLAND B; MCBOGG P; et al. AUTISM AND THE FRAGILE-X SYNDROME | 49 | 63 |
| 1878 | 0 | 1 | 215 1984 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 5(3):160-161 DESPOSITO F THE FRAGILE X-SYNDROME - DIAGNOSIS, BIOCHEMISTRY AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 1879 | 2 | 8 | 216 1984 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 5(4):201-203 KERBESHIAN J; BURD L; MARTSOLF JT FRAGILE X-SYNDROME ASSOCIATED WITH TOURETTE SYMPTOMATOLOGY IN A MALE WITH MODERATE MENTAL-RETARDATION AND AUTISM | 4 | 29 |
| 1880 | 6 | 28 | 296 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(2):87-90 VARLEY CK; HOLM VA; EREN MO COGNITIVE AND PSYCHIATRIC VARIABILITY IN 3 BROTHERS WITH FRAGILE X-SYNDROME | 10 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1881 | 2 | 2 | 297 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 KERBESHIAN J; BURD L; MARTSOLF JT THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME | 1 | 1 |
| 1882 | 0 | 3 | 298 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 LAWRENCE RJ THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME | 0 | 0 |
| 1883 | 0 | 0 | 393 1986 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 7(3):201-202 LACHIEWICZ AM; GULLION CM; SPIRIDIGLIOZZI GA; ALYSWORTH AS DECLINE IN IQ SCORES OF YOUNG FRAGILE X-MALES | 0 | 0 |
| 1884 | 8 | 18 | 394 1986 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 7(4):253-256 MADISON LS; WELLS TE; FRISTO TE; BENESCH CG A CONTROLLED-STUDY OF FOLIC-ACID TREATMENT IN 3 FRAGILE-X SYNDROME MALES | 5 | 6 |
| 1885 | 0 | 0 | 1126 1993 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 14(4):282-282 HULL CE; HAGERMAN RJ A STUDY OF THE PHENOTYPE IN HETEROZYGOUS FRAGILE-X FEMALES | 0 | 0 |
| 1886 | 14 | 37 | 1127 1993 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 14(5):328-335 MAZZOCCO MMM; PENNINGTON BF; HAGERMAN RJ THE NEUROCOGNITIVE PHENOTYPE OF FEMALE CARRIERS OF FRAGILE-X - ADDITIONAL EVIDENCE FOR SPECIFICITY | 71 | 90 |
| 1887 | 0 | 0 | 1771 1998 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 19(5):381-381 Taylor RJ; Scharfenaker S; O'Connor R; Lampe M; Kovach T; et al. Severe language impairment in fragile X syndrome: Clinical correlates and treatment approaches | 0 | 0 |
| 1888 | 13 | 39 | 2038 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(4):278-282 Wisbeck JM; Huffman LC; Freund L; Gunnar MR; Davis EP; et al. Cortisol and social stressors in children with fragile X: A pilot study | 9 | 11 |
| 1889 | 6 | 32 | 2039 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(5):315-321 Bailey DB; Skinner D; Hatton D; Roberts J Family experiences and factors associated with the diagnosis of fragile X syndrome | 12 | 15 |
| 1890 | 0 | 1 | 2169 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(5):337-337 Floet AW Children with fragile X syndrome: A parents' guide | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1891 | 13 | 31 | 2170 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):353-359 Myers GF; Mazzocco MMM; Maddalena A; Reiss AL No widespread psychological effect of the fragile X premutation in childhood: Evidence from a preliminary controlled study | 3 | 3 |
| 1892 | 18 | 34 | 2171 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):409-417 Rogers SJ; Wehner EA; Hagerman R The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders | 13 | 24 |
| 1893 | 32 | 51 | 2298 2002 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 23(6):416-423 Loesch DZ; Huggins RM; Bui QM; Epstein JL; Taylor AK; et al. Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile X males and females assessed by robust pedigree analysis | 6 | 6 |
| 1894 | 10 | 57 | 2438 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(4):267-275 Johnston C; Hessl D; Blasey C; Eliez S; Erba H; et al. Factors associated with parenting stress in mothers of children with fragile X syndrome | 0 | 1 |
| 1895 | 0 | 0 | 2439 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(5):393-393 Hansen R; Goodlin-Jones B; Nowicki S; Heeren M; Herman K; et al. Behavioral phenotypes in older children with autistic spectrum disorders and fragile X: Similarities and differences | 0 | 0 |
| 1896 | 6 | 36 | 2539 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(1):21-27 Mirrett PL; Bailey DB; Roberts JE; Hatton DD Developmental screening and detection of developmental delays in infants and toddlers with fragile X syndrome | 0 | 0 |
| 1897 | 30 | 54 | 2540 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(6):392-398 Goodlin-Jones BL; Tassone F; Gane LW Autistic spectrum disorder and the fragile X premutation | 0 | 0 |
| 1898 | 1 | 45 | 1909 1999 JOURNAL OF EARLY INTERVENTION 22(2):137-151 Jackson SC; Roberts JE Family and professional congruence in communication assessments of preschool boys with fragile X syndrome | 0 | 0 |
| 1899 | 0 | 29 | 1772 1998 JOURNAL OF EXPERIMENTAL MEDICINE 188(12):2335-2342 Sun SQ; Zhang XH; Tough DF; Sprent J Type I interferon-mediated stimulation of T cells by CgG DNA | 0 | 135 |
| 1900 | 0 | 0 | 2440 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1200-1200 Cotton RW; Word CJ Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1901 | 0 | 0 | 2441 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1201-1201 Clarke GW Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54. | 0 | 0 |
| 1902 | 0 | 0 | 2442 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1202-1202 Thompson WC; Taroni F; Aitken CGG Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54. Author's response | 0 | 0 |
| 1903 | 0 | 1 | 2541 2004 JOURNAL OF FORENSIC SCIENCES 49(1):192-193 Brenner CH; Inman K Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54. | 0 | 0 |
| 1904 | 0 | 3 | 2542 2004 JOURNAL OF FORENSIC SCIENCES 49(1):194-195 Thompson WC; Taroni PF; Aitken CGG 'Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54. - Response | 0 | 0 |
| 1905 | 1 | 13 | 2543 2004 JOURNAL OF HUMAN GENETICS 49(2):97-101 Nagao K; Fujii K; Yamada M; Miyashita T Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes | 0 | 0 |
| 1906 | 16 | 34 | 998 1992 JOURNAL OF INHERITED METABOLIC DISEASE 15(4):532-538 HIRST MC; KNIGHT SM; NAKAHORI Y; ROCHE A; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 1907 | 32 | 57 | 1675 1997 JOURNAL OF INHERITED METABOLIC DISEASE 20(2):139-151 Hoogeveen AT; Oostra BA The fragile X syndrome | 6 | 10 |
| 1908 | 7 | 32 | 2443 2003 JOURNAL OF INTELLECTUAL & DEVELOPMENTAL DISABILITY 28(2):135-144 Richdale AL A descriptive analysis of sleep behaviour in children with Fragile X | 1 | 1 |
| 1909 | 1 | 1 | 1128 1993 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 37:111-111 COOPER M GAZE AVOIDING AND TORSO TURNING IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1910 | 7 | 23 | 1129 1993 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 37:131-142 BUTLER MG; SINGH DN CLINICAL AND CYTOGENETIC SURVEY OF INSTITUTIONALIZED MENTALLY-RETARDED PATIENTS WITH EMPHASIS ON THE FRAGILE-X SYNDROME | 4 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1911 | 0 | 0 | 1130 1993 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 37:201-202 RAEBURN S PIECING TOGETHER THE FRAGILE-X - FRAGILE-X WORKSHOP, ROYAL-SOCIETY-OF-MEDICINE, LONDON, ENGLAND, 1 JULY 1992 | 0 | 0 |
| 1912 | 9 | 20 | 1256 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:1-8 DEVRIES LBA; HALLEY DJJ; OOSTRA BA; NIERMEIJER MF THE FRAGILE-X SYNDROME - A GROWING GENE CAUSING FAMILIAL INTELLECTUAL DISABILITY | 1 | 2 |
| 1913 | 16 | 27 | 1257 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:27-35 SABARATNAM M; LAVER S; BUTLER L; PEMBREY M FRAGILE-X SYNDROME IN NORTH-EAST ESSEX - TOWARDS SYSTEMATIC SCREENING - CLINICAL-SELECTION | 6 | 8 |
| 1914 | 2 | 14 | 1409 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:326-330 SIMON EW; RAPPAPORT DA; PAPKA M; WOODRUFFPAK DS FRAGILE-X AND DOWNS-SYNDROME - ARE THERE SYNDROME-SPECIFIC COGNITIVE PROFILES AT LOW IQ LEVELS | 2 | 4 |
| 1915 | 15 | 26 | 1410 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:544-553 Butler MG; Pratesi R; VnencakJones CL Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome | 0 | 1 |
| 1916 | 24 | 41 | 1773 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:81-89 Elbaz A; Suedois J; Duquesnoy M; Beldjord C; Berchel C; et al. Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies | 6 | 8 |
| 1917 | 17 | 41 | 1774 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:490-499 Turk J; Cornish K Face recognition and emotion perception in boys with fragile-X syndrome | 12 | 18 |
| 1918 | 8 | 10 | 1910 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:47-53 Carmichael B; Pembrey M; Turner G; Barnicoat A Diagnosis of fragile-X syndrome: the experiences of parents | 9 | 11 |
| 1919 | 19 | 34 | 1911 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:314-324 York A; von Fraunhofer N; Turk J; Sedgwick P Fragile-X syndrome, Down's syndrome and autism: awareness and knowledge amongst special educators | 2 | 4 |
| 1920 | 11 | 42 | 1912 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:466-474 Garner C; Callias M; Turk J Executive function and theory of mind performance of boys with fragile-X syndrome | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1921 | 8 | 16 | 2040 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:81-85 Sabaratnam M Pathological and neuropathological findings in two males with fragile-X syndrome | 2 | 4 |
| 1922 | 0 | 0 | 2041 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:189-189 Abbeduto L; Kesin E; Pavetto M; Weissman M; O'Brien A; et al. Theory of mind deficits in mental retardation: a comparison of Down syndrome and fragile-X syndrome | 0 | 0 |
| 1923 | 0 | 0 | 2042 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:222-222 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; et al. Progress fragile-X syndrome analysis | 0 | 0 |
| 1924 | 0 | 0 | 2043 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:247-247 Cornish KM; Munir F Profile of memory and attention problems in adults with fragile-X syndrome: Clinical and educational implications | 0 | 0 |
| 1925 | 0 | 0 | 2044 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:273-273 Einfeld SL; Tonge B; Turner G; Parmenter T; Smith A Longitudinal course of behavioural and emotional problems of young persons with Prader-Willi, fragile-X, Williams and Down syndromes | 0 | 0 |
| 1926 | 0 | 0 | 2045 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:305-305 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; et al. Influence of stimulants on electrodermal studies in fragile-X syndrome | 0 | 0 |
| 1927 | 0 | 0 | 2046 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:317-317 Karrer JH; Hagerman RJ; Karrer RS; Fitzpatrick D; Vavold J; et al. Genotypic-specific event-related brain potentials among infants and toddlers with fragile-X syndrome and Down syndrome | 1 | 1 |
| 1928 | 0 | 0 | 2047 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:318-318 Hills JL; Wilson R; Sobesky W; Harris SW; Grigsby J; et al. Executive functioning deficits in adult males with the fragile-X premutation: an emerging phenotype | 0 | 0 |
| 1929 | 0 | 0 | 2048 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:374-374 Lung FW; Shu BC Fragile-X syndrome in adolescent prostitutes | 0 | 0 |
| 1930 | 0 | 0 | 2049 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:380-380 Manjunatha KR; Chettn GK; Arathi R; Bhaskar RG; Nandini PM; et al. Fragile-X syndrome: Cytogenetics and molecular analysis of subjects from Indian population | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1931 | 0 | 0 | 2050 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:405-405 Munir F; Comish KM; Wilding J A neuropsychological profile of attention and hyperactivity in boys with fragile-X syndrome: Implications for clinical intervention | 0 | 0 |
| 1932 | 0 | 0 | 2051 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:419-419 Orsmond G; Abbeduto L; Pavetto M; O'Brien A; Kesin E; et al. Stress and coping in parents of adolescents and young adults with fragile-X syndrome or Down syndrome | 0 | 0 |
| 1933 | 0 | 0 | 2052 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:449-449 Sabaratnam M; Murthy V; Wijeratne A Fragile-X syndrome: A 10-year follow-up | 0 | 0 |
| 1934 | 0 | 0 | 2053 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:483-483 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; et al. FMRI messenger RNA levels in male subjects with fragile-X syndrome | 0 | 0 |
| 1935 | 0 | 0 | 2054 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:496-497 Tzeng CC; Lin SJ; Chen YY; Chen RM An effective strategy of using a molecular test to screen individuals with mental retardation for fragile-X syndrome | 0 | 0 |
| 1936 | 6 | 29 | 2299 2002 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 46:328-339 Kuo AY; Reiss AL; Freund LS; Huffman LC Family environment and cognitive abilities in girls with fragile-X syndrome | 2 | 3 |
| 1937 | 0 | 0 | 2544 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:287-287 Brown W; Nolin S; Dobkin C; Houck G; Glicksman A; et al. Frequency of fragile X in multiplex autism: Testing the AGRE families | 0 | 0 |
| 1938 | 0 | 0 | 2545 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:288-288 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; et al. The fragile X syndrome (FXS): Screening and prenatal diagnosis | 0 | 0 |
| 1939 | 0 | 0 | 2546 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:294-294 Turk J; Das D; Howlin P; Barber N; Mottaleb M; et al. A follow-up of intellectual, social, communicatory & adaptive functioning in boys & young men with fragile X syndrome | 0 | 0 |
| 1940 | 0 | 0 | 2547 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:294-294 Einfeld SL; Tonge BJ; Turner G; Smith E Longitudinal course of behavioural and emotional problems in Prader-Willi, Fragile X, Williams and Down syndromes | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1941 | 0 | 0 | 2548 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:324-324 Abbeduto L; Murphy MM Language, communication, and the behavioural phenotype of Down syndrome (DS): Insights from fragile X syndrome (FXS) and typical development | 0 | 0 |
| 1942 | 0 | 0 | 2549 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:325-325 Abbeduto L; Murphy MM; Giles N; Bruno L; Richmond EK; et al. Understanding language in context: Comparisons of Down syndrome (DS) with fragile X syndrome and typical development | 0 | 0 |
| 1943 | 3 | 35 | 1775 1998 JOURNAL OF INTERFERON AND CYTOKINE RESEARCH 18(8):609-616 Xu Z; Williams BRG Genomic features of human PKR: Alternative splicing and a polymorphic CGG repeat in the 5 '-untranslated region | 0 | 5 |
| 1944 | 0 | 0 | 1549 1996 JOURNAL OF INVESTIGATIVE MEDICINE 44(1):A119-A119 Merenstein SA; Sobesky WE; Taylor AK; Tran HX; Riddle JE; et al. Molecular clinical correlations in males with fragile X syndrome. | 0 | 0 |
| 1945 | 0 | 0 | 1776 1998 JOURNAL OF INVESTIGATIVE MEDICINE 46(1):87A-87A Miller LJ; McIntosh D; McGrath J; Shyu V; Lampe M; et al. Electrodermal responses to sensory stimuli in individuals with fragile X sydrome. | 0 | 0 |
| 1946 | 0 | 0 | 2055 2000 JOURNAL OF INVESTIGATIVE MEDICINE 48(1):11A-11A Peterson TL; Hagerman RJ; Tassone F Genotype-phenotype relationships in fragile X families. | 0 | 0 |
| 1947 | 0 | 0 | 2550 2004 JOURNAL OF INVESTIGATIVE MEDICINE 52(1):S101-S101 Nowicki ST; Jacquemont S; Li L; Nguyen DV; Gregg JP; et al. An approach to identify epistatic genes involved in the development of autism spectrum disorder in patients with fragile X syndrome | 0 | 0 |
| 1948 | 18 | 24 | 2172 2001 JOURNAL OF KOREAN MEDICAL SCIENCE 16(3):271-275 Kwon SH; Lee KS; Hyun MC; Song KE; Kim JK Molecular screening for Fragile X syndrome in mentally handicapped children in Korea | 0 | 0 |
| 1949 | 11 | 91 | 2173 2001 JOURNAL OF LEARNING DISABILITIES 34(6):520-533 Mazzocco MMM Math learning disability and math LD subtypes: Evidence from studies of Turner syndrome, fragile X syndrome, and neurofibromatosis type 1 | 2 | 8 |
| 1950 | 0 | 33 | 1777 1998 JOURNAL OF LUMINESCENCE 79(1):1-8 Padlyak BV; Koepke C; Wisniewski K; Grinberg M; Gutsze A; et al. Spectroscopic evaluation of the CGG (CaO-Ga2O3-GeO2) glass doped with chromium | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1951 | 0 | 23 | 24 1981 JOURNAL OF MEDICAL GENETICS 18(5):366-373 PROOPS R; WEBB T THE FRAGILE X-CHROMOSOME IN THE MARTIN-BELL-RENPENNING SYNDROME AND IN MALES WITH OTHER FORMS OF FAMILIAL MENTAL-RETARDATION | 20 | 32 |
| 1952 | 0 | 15 | 73 1982 JOURNAL OF MEDICAL GENETICS 19(1):44-48 WEBB GC; HALLIDAY JL; PITT DB; JUDGE CG; LEVERSHA M FRAGILE (X)(Q27) SITES IN A PEDIGREE WITH FEMALE CARRIERS SHOWING MILD TO SEVERE MENTAL-RETARDATION | 19 | 36 |
| 1953 | 0 | 0 | 74 1982 JOURNAL OF MEDICAL GENETICS 19(1):64-64 DAKER MG; CHIDIAC P; FEAR CN; BERRY AC FRAGILE X-CHROMOSOME IN BROTHERS WITH NORMAL INTELLIGENCE, OR THE MAN WHO MIGHT HAVE BEEN A GENIUS | 0 | 2 |
| 1954 | 0 | 0 | 75 1982 JOURNAL OF MEDICAL GENETICS 19(5):371-371 WILLATT LR; DAVIS J FRAGILE-X MENTAL-RETARDATION IN TWINS - A CASE-HISTORY | 0 | 0 |
| 1955 | 8 | 31 | 146 1983 JOURNAL OF MEDICAL GENETICS 20(3):169-178 MCDERMOTT A; WALTERS R; HOWELL RT; GARDNER A FRAGILE X-CHROMOSOME - CLINICAL AND CYTOGENETIC STUDIES ON CASES FROM 7 FAMILIES | 14 | 18 |
| 1956 | 0 | 11 | 147 1983 JOURNAL OF MEDICAL GENETICS 20(4):280-285 HARRISON CJ; JACK EM; ALLEN TD; HARRIS R THE FRAGILE X - A SCANNING ELECTRON-MICROSCOPE STUDY | 27 | 54 |
| 1957 | 4 | 12 | 148 1983 JOURNAL OF MEDICAL GENETICS 20(4):286-289 VANROY BC; DESMEDT MC; RAES RA; DUMON JE; LEROY JG FRAGILE X TRAIT IN A LARGE KINDRED - TRANSMISSION ALSO THROUGH NORMAL MALES | 22 | 32 |
| 1958 | 3 | 9 | 149 1983 JOURNAL OF MEDICAL GENETICS 20(4):314-315 HUNTER AGW; MACDONALD J; EVANS JA ABSENCE OF THE FRAGILE-X IN A GROUP OF PATIENTS WITH IDIOPATHIC MENTAL-RETARDATION | 0 | 0 |
| 1959 | 5 | 25 | 150 1983 JOURNAL OF MEDICAL GENETICS 20(6):404-407 VEKEMANS M; POPOVICH B; ROSENBLATT D; MONROE P CHROMOSOMAL BREAKAGE IN NORMAL AND FRAGILE-X SUBJECTS USING LOW FOLATE CULTURE CONDITIONS | 12 | 21 |
| 1960 | 0 | 1 | 151 1983 JOURNAL OF MEDICAL GENETICS 20(6):476-476 MORICPETROVIC S; LACA Z A FATHER AND DAUGHTER WITH FRAGILE X-CHROMOSOME | 6 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1961 | 1 | 3 | 217 1984 JOURNAL OF MEDICAL GENETICS 21(1):74-75 SUTHERLAND GR ROUTINE DIAGNOSTIC-DETECTION OF THE FRAGILE X | 1 | 4 |
| 1962 | 32 | 83 | 218 1984 JOURNAL OF MEDICAL GENETICS 21(2):84-91 DEARCE MA; KEARNS A THE FRAGILE X-SYNDROME - THE PATIENTS AND THEIR CHROMOSOMES | 9 | 20 |
| 1963 | 0 | 0 | 219 1984 JOURNAL OF MEDICAL GENETICS 21(4):298-298 WEBB TP; BUNDEY SE; THAKE A; TODD J STUDY OF THE FRAGILE X-CHROMOSOME AND MENTAL-RETARDATION | 0 | 3 |
| 1964 | 0 | 0 | 220 1984 JOURNAL OF MEDICAL GENETICS 21(4):299-299 PEMBREY ME; WINTER RM; DAVIES KE A PERMUTATION THAT GENERATES THE DEFINITIVE MUTATION BY RECOMBINATION EXPLAINS THE INHERITANCE OF THE MARTIN-BELL SYNDROME (FRAGILE-X) | 9 | 13 |
| 1965 | 0 | 4 | 221 1984 JOURNAL OF MEDICAL GENETICS 21(5):373-373 FITCHETT M; SEABRIGHT M DELETED X-CHROMOSOMES IN PATIENTS WITH THE FRAGILE X-SYNDROME | 10 | 14 |
| 1966 | 3 | 15 | 299 1985 JOURNAL OF MEDICAL GENETICS 22(2):85-91 TUCKERMAN E; WEBB T; BUNDEY SE FREQUENCY AND REPLICATION STATUS OF THE FRAGILE-X, FRA(X)(Q27-28), IN A PAIR OF MONOZYGOTIC TWINS OF MARKEDLY DIFFERING INTELLIGENCE | 21 | 36 |
| 1967 | 5 | 29 | 300 1985 JOURNAL OF MEDICAL GENETICS 22(4):258-266 BUNDEY S; WEBB TP; THAKE A; TODD J A COMMUNITY STUDY OF SEVERE MENTAL-RETARDATION IN THE WEST MIDLANDS AND THE IMPORTANCE OF THE FRAGILE X-CHROMOSOME IN ITS ETIOLOGY | 16 | 32 |
| 1968 | 1 | 4 | 301 1985 JOURNAL OF MEDICAL GENETICS 22(5):397-397 WINTER RM; PEMBREY ME; DAVIES KE ANALYSIS OF LINKAGE DATA WITH FACTOR-IX CORROBORATES THE HYPOTHESIS THAT A PREMUTATION, FOLLOWED BY A RECOMBINATION EVENT, GENERATES THE FULL MUTATION IN FRAGILE X-LINKED MENTAL-RETARDATION | 2 | 2 |
| 1969 | 0 | 0 | 395 1986 JOURNAL OF MEDICAL GENETICS 23(2):166-166 WEBB TP; BUNDEY SE; THAKE A; TODD J THE PREVALENCE OF THE FRAGILE-X SYNDROME IN SCHOOLCHILDREN IN COVENTRY | 0 | 0 |
| 1970 | 0 | 0 | 396 1986 JOURNAL OF MEDICAL GENETICS 23(2):166-167 CONNOR JM; COLGAN JM; CROSSLEY JA; IMRIE SJ; YATES JRW MULTIPOINT LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE-X SYNDROME | 2 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1971 | 4 | 11 | 397 1986 JOURNAL OF MEDICAL GENETICS 23(5):396-399 WEBB TP; BUNDEY S; THAKE A; TODD J THE FREQUENCY OF THE FRAGILE X-CHROMOSOME AMONG SCHOOLCHILDREN IN COVENTRY | 70 | 105 |
| 1972 | 9 | 16 | 398 1986 JOURNAL OF MEDICAL GENETICS 23(5):400-406 WEBB T; THAKE A; TODD J 12 FAMILIES WITH FRAGILE X(Q27) | 7 | 8 |
| 1973 | 6 | 13 | 399 1986 JOURNAL OF MEDICAL GENETICS 23(5):407-410 TUCKERMAN E; WEBB T; THAKE A REPLICATION STATUS OF FRAGILE X(Q27.3) IN 13 FEMALE HETEROZYGOTES | 12 | 16 |
| 1974 | 16 | 41 | 472 1987 JOURNAL OF MEDICAL GENETICS 24(1):14-22 CONNOR JM; PIRRIT LA; YATES JRW; CROSSLEY JA; IMRIE SJ; et al. LINKAGE ANALYSIS USING MULTIPLE XQ DNA POLYMORPHISMS IN NORMAL-FAMILIES, FAMILIES WITH THE FRAGILE X-SYNDROME, AND OTHER FAMILIES WITH X-LINKED CONDITIONS | 7 | 12 |
| 1975 | 17 | 38 | 473 1987 JOURNAL OF MEDICAL GENETICS 24(1):23-31 VEENEMA H; GERAEDTS JPM; BEVERSTOCK GC; PEARSON PL THE FRAGILE X-SYNDROME IN A LARGE FAMILY .1. CYTOGENETIC AND CLINICAL INVESTIGATIONS | 14 | 21 |
| 1976 | 5 | 21 | 474 1987 JOURNAL OF MEDICAL GENETICS 24(1):32-38 VEENEMA H; VEENEMA T; GERAEDTS JPM THE FRAGILE X-SYNDROME IN A LARGE FAMILY .2. PSYCHOLOGICAL INVESTIGATIONS | 29 | 40 |
| 1977 | 0 | 0 | 475 1987 JOURNAL OF MEDICAL GENETICS 24(4):240-240 WINTER RM POPULATION-GENETICS IMPLICATIONS OF THE PREMUTATION HYPOTHESIS FOR THE GENERATION OF THE FRAGILE-X MENTAL-RETARDATION GENE | 0 | 0 |
| 1978 | 13 | 33 | 476 1987 JOURNAL OF MEDICAL GENETICS 24(7):413-421 VEENEMA H; CARPENTER NJ; BAKKER E; HOFKER MH; WARD AM; et al. THE FRAGILE-X SYNDROME IN A LARGE FAMILY .3. INVESTIGATIONS ON LINKAGE OF FLANKING DNA MARKERS WITH THE FRAGILE SITE-XQ27 | 17 | 38 |
| 1979 | 0 | 0 | 477 1987 JOURNAL OF MEDICAL GENETICS 24(10):635-635 CONNOR JM; OSMAN H; STEPHANIE L; NEVIN NC; HOFKER M LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE X SYNDROME USING CX55-7 (DXS105) | 3 | 3 |
| 1980 | 0 | 0 | 478 1987 JOURNAL OF MEDICAL GENETICS 24(10):640-640 SENIOR J; KILPATRICK M; WEBB T COMPARATIVE LINKAGE STUDIES IN THE FRAGILE X-SYNDROME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1981 | 0 | 0 | 479 1987 JOURNAL OF MEDICAL GENETICS 24(10):641-641 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 1 | 1 |
| 1982 | 1 | 1 | 605 1988 JOURNAL OF MEDICAL GENETICS 25(1):64-64 LACA Z; BRANKOVIC S EXPRESSION OF FRAGILE X-CHROMOSOME AND POSSIBLE DELETION IN SUCCESSIVE CELL DIVISIONS | 0 | 0 |
| 1983 | 0 | 0 | 606 1988 JOURNAL OF MEDICAL GENETICS 25(2):128-128 ENGLISH C ANTHROPOMETRIC STUDIES IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 1984 | 0 | 0 | 607 1988 JOURNAL OF MEDICAL GENETICS 25(2):129-129 DAVIES KE; PATTERSON M; BELL M; KENWRICK SJ MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 1985 | 0 | 0 | 608 1988 JOURNAL OF MEDICAL GENETICS 25(2):131-131 MCKINLEY MJ; KEARNEY LU; NICOLAIDES K PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY PLACENTAL BIOPSY | 0 | 0 |
| 1986 | 5 | 17 | 609 1988 JOURNAL OF MEDICAL GENETICS 25(6):407-414 LOESCH DZ; HAY DA CLINICAL-FEATURES AND REPRODUCTIVE PATTERNS IN FRAGILE-X FEMALE HETEROZYGOTES | 33 | 43 |
| 1987 | 4 | 9 | 653 1989 JOURNAL OF MEDICAL GENETICS 26(7):439-442 VOULLAIRE LE; WEBB GC; LEVERSHA M FRAGILE X-TESTING IN A DIAGNOSTIC CYTOGENETICS LABORATORY | 3 | 7 |
| 1988 | 0 | 0 | 716 1990 JOURNAL OF MEDICAL GENETICS 27(3):208-208 GLASS IA; WHITE EM; PIRRIT LA; BELL MV; CONNOR JM LINKAGE STUDY OF F8 IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1989 | 0 | 0 | 717 1990 JOURNAL OF MEDICAL GENETICS 27(3):208-209 WEBB T PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1990 | 4 | 4 | 874 1991 JOURNAL OF MEDICAL GENETICS 28(5):358-358 WEBB T; BUNDEY S PREVALENCE OF FRAGILE X-SYNDROME | 6 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1991 | 0 | 0 | 875 1991 JOURNAL OF MEDICAL GENETICS 28(12):809-810 JACOBS PA THE FRAGILE-X SYNDROME | 6 | 10 |
| 1992 | 6 | 9 | 876 1991 JOURNAL OF MEDICAL GENETICS 28(12):811-813 CONNOR JM CLONING OF THE GENE FOR THE FRAGILE-X SYNDROME - IMPLICATIONS FOR THE CLINICAL GENETICIST | 1 | 1 |
| 1993 | 6 | 6 | 877 1991 JOURNAL OF MEDICAL GENETICS 28(12):814-817 WEBB T MOLECULAR-GENETICS OF FRAGILE-X - A CYTOGENETICS VIEWPOINT - REPORT OF THE 5TH INTERNATIONAL-SYMPOSIUM ON X-LINKED MENTAL-RETARDATION, STRASBOURG, FRANCE, 12 TO 16 AUGUST 1991 | 3 | 7 |
| 1994 | 5 | 10 | 878 1991 JOURNAL OF MEDICAL GENETICS 28(12):818-823 RICHARDS RI; HOLMAN K; KOZMAN H; KREMER E; LYNCH M; et al. FRAGILE-X SYNDROME - GENETIC LOCALIZATION BY LINKAGE MAPPING OF 2 MICROSATELLITE REPEATS FRAXAC1 AND FRAXAC2 WHICH IMMEDIATELY FLANK THE FRAGILE SITE | 63 | 102 |
| 1995 | 11 | 17 | 879 1991 JOURNAL OF MEDICAL GENETICS 28(12):824-829 HIRST MC; NAKAHORI Y; KNIGHT SJL; SCHWARTZ C; THIBODEAU SN; et al. GENOTYPE PREDICTION IN THE FRAGILE-X SYNDROME | 27 | 36 |
| 1996 | 11 | 20 | 880 1991 JOURNAL OF MEDICAL GENETICS 28(12):830-836 ROUSSEAU F; HEITZ D; OBERLE I; MANDEL JL SELECTION IN BLOOD-CELLS FROM FEMALE CARRIERS OF THE FRAGILE-X SYNDROME - INVERSE CORRELATION BETWEEN AGE AND PROPORTION OF ACTIVE X-CHROMOSOMES CARRYING THE FULL MUTATION | 64 | 86 |
| 1997 | 1 | 6 | 881 1991 JOURNAL OF MEDICAL GENETICS 28(12):837-839 GRIFFITHS MJ; STRACHAN MC A SINGLE LYMPHOCYTE CULTURE FOR FRAGILE-X INDUCTION AND PROMETAPHASE CHROMOSOME ANALYSIS | 0 | 1 |
| 1998 | 2 | 2 | 999 1992 JOURNAL OF MEDICAL GENETICS 29(4):287-287 SMART RD FRAGILE X-SYNDROME - AS COMMON AS 1ST THOUGHT | 3 | 4 |
| 1999 | 14 | 20 | 1000 1992 JOURNAL OF MEDICAL GENETICS 29(6):368-374 MULLEY JC; YU S; GEDEON AK; DONNELLY A; TURNER G; et al. EXPERIENCE WITH DIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X | 28 | 39 |
| 2000 | 3 | 10 | 1001 1992 JOURNAL OF MEDICAL GENETICS 29(8):599-599 TIZZANO EF; BAIGET M HIGH PROPORTION OF TWINS IN CARRIERS OF FRAGILE X-SYNDROME | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2001 | 7 | 8 | 1002 1992 JOURNAL OF MEDICAL GENETICS 29(10):726-729 TARLETON J; WONG S; HEITZ D; SCHWARTZ C DIFFICULT DIAGNOSIS OF THE FRAGILE X-SYNDROME MADE POSSIBLE BY DIRECT DETECTION OF DNA MUTATIONS | 1 | 1 |
| 2002 | 23 | 34 | 1003 1992 JOURNAL OF MEDICAL GENETICS 29(11):794-801 HEITZ D; DEVYS D; IMBERT G; KRETZ C; MANDEL JL INHERITANCE OF THE FRAGILE-X SYNDROME - SIZE OF THE FRAGILE-X PREMUTATION IS A MAJOR DETERMINANT OF THE TRANSITION TO FULL MUTATION | 84 | 111 |
| 2003 | 8 | 9 | 1004 1992 JOURNAL OF MEDICAL GENETICS 29(12):919-920 TARLETON J; WONG S; SCHWARTZ C DIRECT ANALYSIS OF THE FMR-1 GENE PROVIDES AN EXPLANATION FOR AN EXCEPTIONAL CASE OF A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE IN A FRAGILE-X FAMILY | 1 | 2 |
| 2004 | 10 | 13 | 1131 1993 JOURNAL OF MEDICAL GENETICS 30(2):94-96 SMITS APT; DREESEN JCFM; POST JG; SMEETS DFCM; DEDIESMULDERS C; et al. THE FRAGILE-X SYNDROME - NO EVIDENCE FOR ANY RECENT MUTATIONS | 27 | 35 |
| 2005 | 10 | 11 | 1132 1993 JOURNAL OF MEDICAL GENETICS 30(3):193-197 KNOBLOCH O; PELZ F; WICK U; NELSON DL; ZOLL B DIRECT VERSUS INDIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X MENTAL-RETARDATION IN 40 GERMAN FAMILIES AT RISK | 1 | 1 |
| 2006 | 22 | 25 | 1133 1993 JOURNAL OF MEDICAL GENETICS 30(5):410-413 OOSTRA BA; JACKY PB; BROWN WT; ROUSSEAU F GUIDELINES FOR THE DIAGNOSIS OF FRAGILE-X SYNDROME | 49 | 61 |
| 2007 | 7 | 12 | 1134 1993 JOURNAL OF MEDICAL GENETICS 30(6):454-459 JACOBS PA; BULLMAN H; MACPHERSON J; YOUINGS S; ROONEY V; et al. POPULATION STUDIES OF THE FRAGILE-X - A MOLECULAR APPROACH | 55 | 81 |
| 2008 | 15 | 29 | 1135 1993 JOURNAL OF MEDICAL GENETICS 30(8):647-650 HIRST MC; KNIGHT SJL; CHRISTODOULOU Z; GREWAL PK; FRYNS JP; et al. ORIGINS OF THE FRAGILE-X SYNDROME MUTATION | 22 | 33 |
| 2009 | 10 | 27 | 1136 1993 JOURNAL OF MEDICAL GENETICS 30(9):761-766 DEVRIES BBA; FRYNS JP; BUTLER MG; CANZIANI F; WESBYVANSWAAY E; et al. CLINICAL AND MOLECULAR STUDIES IN FRAGILE-X PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE | 19 | 33 |
| 2010 | 7 | 9 | 1137 1993 JOURNAL OF MEDICAL GENETICS 30(9):785-787 SUZUMORI K; YAMAUCHI M; SEKI N; KONDO I; HORI T PRENATAL-DIAGNOSIS OF A HYPERMETHYLATED FULL FRAGILE-X MUTATION IN CHORIONIC VILLI OF A MALE FETUS | 1 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2011 | 3 | 8 | 1258 1994 JOURNAL OF MEDICAL GENETICS 31(1):76-78 TEJADA MI; MORNET E; TIZZANO E; MOLINA M; BAIGET M; et al. IDENTIFICATION BY MOLECULAR DIAGNOSIS OF MOSAIC TURNERS-SYNDROME IN AN OBLIGATE CARRIER FEMALE FOR FRAGILE-X SYNDROME | 4 | 8 |
| 2012 | 0 | 0 | 1259 1994 JOURNAL OF MEDICAL GENETICS 31(2):170-170 STRAIN L; PORTEOUS MEM; BONTHRON DT PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION | 0 | 0 |
| 2013 | 0 | 0 | 1260 1994 JOURNAL OF MEDICAL GENETICS 31(2):173-173 WANG Q; GREEN EP; MATHEW CG; BOBROW M NONRADIOACTIVE PCR BASED SCREENING FOR FRAGILE-X SYNDROME | 0 | 0 |
| 2014 | 0 | 0 | 1261 1994 JOURNAL OF MEDICAL GENETICS 31(2):173-173 BULLOCK S; LINDLEY V COMPLEMENTARY CYTOGENETIC AND MOLECULAR ANALYSIS OF A REFERRAL FOR FRAGILE-X TESTING | 0 | 0 |
| 2015 | 1 | 3 | 1262 1994 JOURNAL OF MEDICAL GENETICS 31(3):260-261 GILLESSENKAESBACH G; HORSTHEMKE B CLINICAL AND MOLECULAR STUDIES IN FRAGILE-X PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE | 0 | 3 |
| 2016 | 1 | 2 | 1263 1994 JOURNAL OF MEDICAL GENETICS 31(10):820-820 DEVRIES BBA; NIERMEIJER MF THE PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X PATIENTS - A DESIGNATION FACILITATING CLINICAL (AND MOLECULAR) DIFFERENTIAL-DIAGNOSIS | 1 | 6 |
| 2017 | 6 | 12 | 1264 1994 JOURNAL OF MEDICAL GENETICS 31(12):950-952 CURTIS G; DENNIS N; MACPHERSON J THE IMPACT OF GENETIC-COUNSELING ON FEMALES IN FRAGILE-X FAMILIES | 1 | 1 |
| 2018 | 0 | 0 | 1411 1995 JOURNAL OF MEDICAL GENETICS 32(2):144-145 MORTON JE; RINDL PM; BULLOCK S; BUNDEY S; WEBB T FRAGILE-X SYNDROME IS LESS COMMON THAN PREVIOUSLY ESTIMATED | 2 | 2 |
| 2019 | 0 | 0 | 1412 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 WANG Q; GREEN EP; BOBROW M; MATHEW CG SCREENING FOR THE FRAGILE-X A-MUTATION AND E-MUTATION BY AUTOMATED FLUORESCENT ANALYSIS | 0 | 0 |
| 2020 | 0 | 0 | 1413 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 BULLOCK S; LINDLEY VH; STEVENSON K; COLE T MOLECULAR DNA TESTING OF A FAMILY MANIFESTING FRAGILE-X SYNDROME IN BOTH THE FRAX-A FULL MUTATION AND MOSAIC FORMS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2021 | 0 | 0 | 1414 1995 JOURNAL OF MEDICAL GENETICS 32(2):154-154 BULLOCK S; FELIX CA; BUTTERWORTH MA; STEVENSON K; WILLIAMS D THE USE OF MOLECULAR DNA TESTING TO DISTINGUISH BETWEEN MUTATIONS AT THE FRAGILE-X A-SITES AND E-SITES | 0 | 0 |
| 2022 | 10 | 20 | 1415 1995 JOURNAL OF MEDICAL GENETICS 32(3):170-173 WANG Q; GREEN E; BOBROW M; MATHEW CG A RAPID, NONRADIOACTIVE SCREENING-TEST FOR FRAGILE-X MUTATIONS AT THE FRAXA AND FRAXE LOCI | 17 | 28 |
| 2023 | 17 | 27 | 1416 1995 JOURNAL OF MEDICAL GENETICS 32(3):236-239 MACPHERSON JN; CURTIS G; CROLLA JA; DENNIS N; MIGEON B; et al. UNUSUAL (CGG)(N) EXPANSION AND RECOMBINATION IN A FAMILY WITH FRAGILE-X AND DIGEORGE-SYNDROME | 5 | 11 |
| 2024 | 16 | 40 | 1417 1995 JOURNAL OF MEDICAL GENETICS 32(10):764-769 DEVRIES BBA; ROBINSON H; STOLTEDIJKSTRA I; GI CVTP; DIJKSTRA PF; et al. GENERAL OVERGROWTH IN THE FRAGILE-X SYNDROME - VARIABILITY IN THE PHENOTYPIC-EXPRESSION OF THE FMR1 GENE MUTATION | 6 | 16 |
| 2025 | 8 | 12 | 1418 1995 JOURNAL OF MEDICAL GENETICS 32(11):907-908 PINTADO E; DEDIEGO Y; HMADCHA A; CARRASCO M; SIERRA J; et al. INSTABILITY OF THE CGG REPEAT AT THE FRAXA LOCUS AND VARIABLE PHENOTYPIC-EXPRESSION IN A LARGE FRAGILE-X PEDIGREE | 2 | 9 |
| 2026 | 14 | 35 | 1419 1995 JOURNAL OF MEDICAL GENETICS 32(12):925-929 KIRCHGESSNER CU; WARREN ST; WILLARD HF X INACTIVATION OF THE FMR1 FRAGILE-X MENTAL-RETARDATION GENE | 5 | 13 |
| 2027 | 10 | 13 | 1550 1996 JOURNAL OF MEDICAL GENETICS 33(4):338-340 Mila M; CastellviBel S; Sanchez A; Lazaro C; Villa M; et al. Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene | 11 | 16 |
| 2028 | 15 | 21 | 1551 1996 JOURNAL OF MEDICAL GENETICS 33(5):376-378 Wang ZM; Taylor AK; Bridge JA FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 17 | 22 |
| 2029 | 13 | 20 | 1552 1996 JOURNAL OF MEDICAL GENETICS 33(12):1007-1010 deVries BBA; Jansen CCAM; Duits AA; Verheij C; Willemsen R; et al. Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family | 31 | 38 |
| 2030 | 0 | 0 | 1676 1997 JOURNAL OF MEDICAL GENETICS 34:SP69-SP69 Webb J; Murray A; Conway G; Jacobs P Premature ovarian failure and fragile X | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2031 | 0 | 0 | 1677 1997 JOURNAL OF MEDICAL GENETICS 34:505-505 Brady AF; Suri M; Emerson J; Bell J; Chotai K; et al. Unusual X chromosome inactivation resulting in fragile X phenotype in a girl with a deletion on (X)(q26q27) | 0 | 0 |
| 2032 | 0 | 0 | 1678 1997 JOURNAL OF MEDICAL GENETICS 34:531-531 Cottrell S; Redmond E; McMahon C; Genet S; Barnicoat A Two deletions causing reversal to normal phenotype in fragile X syndrome. | 0 | 0 |
| 2033 | 0 | 0 | 1679 1997 JOURNAL OF MEDICAL GENETICS 34:539-539 Buckingham A; Bell JA; Payne SJ; Masters K; Emmerson J; et al. Recurrence of Turner's syndrome in a fragile-X family | 0 | 0 |
| 2034 | 0 | 0 | 1680 1997 JOURNAL OF MEDICAL GENETICS 34:541-541 Moore S; Dean JCS; Cole GF; Hamilton L; Kelly KF; et al. Fragile X Syndrome resulting from a deletion of the FMR1 gene | 0 | 0 |
| 2035 | 17 | 29 | 1681 1997 JOURNAL OF MEDICAL GENETICS 34(1):1-5 Morton JE; Bundey S; Webb TP; MacDonald F; Rindl PM; et al. Fragile X syndrome is less common than previously estimated | 28 | 47 |
| 2036 | 7 | 10 | 1682 1997 JOURNAL OF MEDICAL GENETICS 34(3):250-251 Willemsen R; Los F; Mohkamsing S; vandenOuweland A; Deelen W; et al. Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A new appraisal | 10 | 12 |
| 2037 | 1 | 2 | 1683 1997 JOURNAL OF MEDICAL GENETICS 34(4):350-350 Loesch DZ FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 1 | 1 |
| 2038 | 0 | 1 | 1684 1997 JOURNAL OF MEDICAL GENETICS 34(4):350-350 Taylor AK FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male - Reply | 0 | 0 |
| 2039 | 21 | 32 | 1685 1997 JOURNAL OF MEDICAL GENETICS 34(8):627-631 Kunst CB; Leeflang EP; Iber JC; Arnheim N; Warren ST The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing | 3 | 16 |
| 2040 | 12 | 38 | 1686 1997 JOURNAL OF MEDICAL GENETICS 34(11):907-911 vanRijn MA; deVries BBA; Tibben A; vandenOuweland AMW; Halley DJJ; et al. DNA testing for fragile X syndrome: implications for parents and family | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2041 | 11 | 15 | 1687 1997 JOURNAL OF MEDICAL GENETICS 34(11):924-926 Losekoot M; Hoogendoorn E; Olmer R; Jansen CCAM; Oosterwijk JC; et al. Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus | 1 | 7 |
| 2042 | 27 | 51 | 1778 1998 JOURNAL OF MEDICAL GENETICS 35(2):103-111 Wohrle D; Salat U; Glaser D; Mucke J; Meisel-Stosiek M; et al. Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats | 19 | 32 |
| 2043 | 140 | 197 | 1779 1998 JOURNAL OF MEDICAL GENETICS 35(7):579-589 de Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF The fragile X syndrome | 32 | 52 |
| 2044 | 5 | 8 | 1780 1998 JOURNAL OF MEDICAL GENETICS 35(10):878-878 Jenkins T; Krause A Molecular evidence that fragile X syndrome occurs in the South African black population | 0 | 0 |
| 2045 | 0 | 0 | 1913 1999 JOURNAL OF MEDICAL GENETICS 36:S64-S64 Lazarau L; Warburton SA; Roberts CE; Hughes HE; Bartlett S; et al. Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male | 0 | 0 |
| 2046 | 0 | 0 | 1914 1999 JOURNAL OF MEDICAL GENETICS 36:S65-S65 Chotai K; Payne SJ A fragile-X male mosaic for normal, premutation and full mutation FMR-1 alleles | 0 | 0 |
| 2047 | 10 | 21 | 1915 1999 JOURNAL OF MEDICAL GENETICS 36(2):167-170 de Vries BBA; van den Boer-van den Berg HMA; Niermeijer MF; Tibben A Dilemmas in Counselling females with the fragile X syndrome | 0 | 1 |
| 2048 | 2 | 5 | 1916 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-171 Macpherson J; Murray A; Webb J; Jacobs P Fragile X syndrome: of POF and premutations | 1 | 2 |
| 2049 | 0 | 0 | 1917 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-172 De Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF Fragile X syndrome: of POF and premutations | 0 | 0 |
| 2050 | 12 | 18 | 1918 1999 JOURNAL OF MEDICAL GENETICS 36(3):253-257 Helderman-van den Enden ATJM; Maaswinkel-Mooij PD; Hoogendoorn E; Willemsen R; Maat-Kievit JA; et al. Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities | 3 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2051 | 16 | 22 | 1919 1999 JOURNAL OF MEDICAL GENETICS 36(6):467-470 de Vries BBA; Mohkamsing S; van den Ouweland AMW; Mol E; Gelsema K; et al. Screening for the fragile X syndrome among the mentally retarded: a clinical study | 4 | 12 |
| 2052 | 5 | 6 | 1920 1999 JOURNAL OF MEDICAL GENETICS 36(7):565-566 Moore SJ; Strain L; Cole GF; Miedzybrodzka Z; Kelly KF; et al. Fragile X syndrome with FMR1 and FMR2 deletion | 1 | 3 |
| 2053 | 0 | 0 | 2056 2000 JOURNAL OF MEDICAL GENETICS 37:S18-S18 Mandel JL The fragile X syndrome: from families to CGG expansions and FMR1 gene function | 0 | 0 |
| 2054 | 0 | 0 | 2057 2000 JOURNAL OF MEDICAL GENETICS 37:S20-S20 Fisher A; Macpherson JN; Dennis NR; Barber JCK Targeted testing for fragile X: an audit of the first year. | 0 | 0 |
| 2055 | 0 | 0 | 2058 2000 JOURNAL OF MEDICAL GENETICS 37:S44-S44 James T; Trigg A; Lindley VH; Fews GA; Roberts E; et al. An unexpected finding of fragile X (FRAXA) syndrome in a fetal blood sample referred for abnormalities on ultrasound scan | 0 | 0 |
| 2056 | 0 | 0 | 2059 2000 JOURNAL OF MEDICAL GENETICS 37:S66-S66 Lazarou LP; Myring J; Knight SJL; Gardner AP; Clarke A Fragile X (E) syndrome. How common is it? | 0 | 0 |
| 2057 | 0 | 0 | 2060 2000 JOURNAL OF MEDICAL GENETICS 37:S75-S75 Fratter C; Morsman A; Seller A Genetic analysis for Fragile X syndrome by fluorescent PCR | 0 | 0 |
| 2058 | 0 | 0 | 2061 2000 JOURNAL OF MEDICAL GENETICS 37:S78-S78 Chotai K; Buckingham AE; Bentley CM; Wycherley RJ; Payne SJ Fragile-X intermediate alleles - A clinical dilemma | 0 | 0 |
| 2059 | 21 | 36 | 2062 2000 JOURNAL OF MEDICAL GENETICS 37(1):77-79 Beresford RG; Tatlidil C; Riddell DC; Welch JP; Ludman MD; et al. Absence of fragile X syndrome in Nova Scotia | 4 | 5 |
| 2060 | 12 | 16 | 2063 2000 JOURNAL OF MEDICAL GENETICS 37(8):603-604 Willemsen R; Olmer R; Otero YD; Oostra BA Twin sisters, monozygotic with the fragile X mutation, but with a different phenotype | 8 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2061 | 39 | 66 | 2064 2000 JOURNAL OF MEDICAL GENETICS 37(11):842-850 Salat U; Bardoni B; Wohrle D; Steinbach P Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations? | 4 | 6 |
| 2062 | 0 | 0 | 2174 2001 JOURNAL OF MEDICAL GENETICS 38:S39-S39 Moore C; Daly EM; Tassone F; Schmitz N; Hagerman P; et al. Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| 2063 | 0 | 0 | 2175 2001 JOURNAL OF MEDICAL GENETICS 38:S40-S40 Daly E; Moore CJ; Schmitz N; Jacobs P; Davies K; et al. Premutation expansion of CGG triplet repeats affects brain; a study of Male Carriers of Fragile X Syndrome | 0 | 0 |
| 2064 | 0 | 0 | 2176 2001 JOURNAL OF MEDICAL GENETICS 38:S63-S63 Warburton S; Waters J; Davison V Targeted diagnostic testing for fragile X syndrome | 0 | 0 |
| 2065 | 0 | 0 | 2177 2001 JOURNAL OF MEDICAL GENETICS 38:S64-S64 Wakeling W; King W; Taylor R Chemiluminescence detection offers a safe, effective and convenient alternative to radioisotopic labelling of probes for detection of Fragile X syndrome and other single gene disorders | 0 | 0 |
| 2066 | 14 | 19 | 2178 2001 JOURNAL OF MEDICAL GENETICS 38(7):453-456 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA | 16 | 22 |
| 2067 | 0 | 0 | 2300 2002 JOURNAL OF MEDICAL GENETICS 39:S73-S73 Bilgen T; Keser I; Mihci E; Tacoy S; Haspolat S; et al. Screening of the FMR1 gene (CCG)n expansion by expand long PCR in families with fragile X syndrome in antalya province. | 0 | 0 |
| 2068 | 0 | 0 | 2301 2002 JOURNAL OF MEDICAL GENETICS 39:S76-S76 Jani A; Hodsdon P; Churchley K; Crocker M; Stefanou E; et al. An atypical week for the Oxford Fragile X service: Two interesting cases | 0 | 0 |
| 2069 | 18 | 20 | 2302 2002 JOURNAL OF MEDICAL GENETICS 39(3):196-200 Tarleton J; Kenneson A; Taylor AK; Crandall K; Fletcher R; et al. A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype | 0 | 0 |
| 2070 | 0 | 0 | 2444 2003 JOURNAL OF MEDICAL GENETICS 40:S15-S15 Ennis S; Collins A; Morton NE SNP-based haplotypes and LD blocks in the fragile X region | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2071 | 0 | 0 | 2445 2003 JOURNAL OF MEDICAL GENETICS 40:S49-S49 Dalton A; Mills AC; Rigby A; Manly T; Hollis C; et al. The neuropsychological phenotype of fragile X premutation males | 0 | 0 |
| 2072 | 0 | 0 | 2446 2003 JOURNAL OF MEDICAL GENETICS 40:S80-S80 Payne S; Powell CM Fragile-X intermediate alleles - instability and inconclusion | 0 | 0 |
| 2073 | 18 | 22 | 2447 2003 JOURNAL OF MEDICAL GENETICS 40(5):377-379 Willemsen R; Smits A; Severijnen LA; Jansen M; Jacobs A; et al. Predictive testing for cognitive functioning in female carriers of the fragile X syndrome using hair root analysis | 3 | 3 |
| 2074 | 28 | 41 | 2448 2003 JOURNAL OF MEDICAL GENETICS 40(7):535-539 de Vries BBA; Severijnen LA; Jacobs A; Olmer R; Halley DJJ; et al. FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics | 1 | 1 |
| 2075 | 0 | 0 | 2551 2004 JOURNAL OF MEDICAL GENETICS 41:S64-S64 Turner A; Myring J; Stephens M; Antoniadi T; Butler R The Problem with Premutations: Assessment of new methods for fragile-X screening. | 0 | 0 |
| 2076 | 0 | 0 | 2552 2004 JOURNAL OF MEDICAL GENETICS 41:S82-S82 McConachie M; Conlin L; McKay F; Gillespie K; Berg J A false negative PCR result in a boy with Fragile X syndrome | 0 | 0 |
| 2077 | 10 | 16 | 2553 2004 JOURNAL OF MEDICAL GENETICS 41(4) Zhou Y; Law HY; Boehm CD; Yoon CS; Cutting GR; et al. Robust fragile X (CGG)(n) genotype classification using a methylation specific triple PCR assay | 0 | 0 |
| 2078 | 12 | 15 | 2554 2004 JOURNAL OF MEDICAL GENETICS 41(4) Tassone F; Hagerman RJ; Garcia-Arocena D; Khandjian EW; Greco CM; et al. Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome | 0 | 2 |
| 2079 | 18 | 28 | 1921 1999 JOURNAL OF MEDICAL SCREENING 6(2):70-76 Wildhagen MF; van Os TAM; Polder JJ; ten Kate LP; Habbema JDF Efficacy of cascade testing for fragile X syndrome | 3 | 5 |
| 2080 | 1 | 7 | 25 1981 JOURNAL OF MENTAL DEFICIENCY RESEARCH 25(DEC):253-& RICHARDS BW; SYLVESTER PE; BROOKER C FRAGILE X-LINKED MENTAL-RETARDATION - THE MARTIN-BELL SYNDROME | 37 | 56 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2081 | 8 | 17 | 152 1983 JOURNAL OF MENTAL DEFICIENCY RESEARCH 27(SEP):211-226 NIELSEN KB DIAGNOSIS OF THE FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) - CLINICAL FINDINGS IN 27 MALES WITH THE FRAGILE SITE AT XQ28 | 18 | 26 |
| 2082 | 6 | 21 | 400 1986 JOURNAL OF MENTAL DEFICIENCY RESEARCH 30:27-39 GILLBERG C; PERSSON E; WAHLSTROM J THE AUTISM-FRAGILE-X SYNDROME (AFRAX) - A POPULATION-BASED STUDY OF 10 BOYS | 14 | 25 |
| 2083 | 6 | 45 | 401 1986 JOURNAL OF MENTAL DEFICIENCY RESEARCH 30:129-148 MADISON LS; GEORGE C; MOESCHLER JB COGNITIVE-FUNCTIONING IN THE FRAGILE-X SYNDROME - A STUDY OF INTELLECTUAL, MEMORY AND COMMUNICATION-SKILLS | 25 | 31 |
| 2084 | 4 | 18 | 480 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:73-79 PUESCHEL SM; OBRIEN MM; PADREMENDOZA T KLINEFELTER SYNDROME AND ASSOCIATED FRAGILE-X SYNDROME | 7 | 8 |
| 2085 | 2 | 4 | 481 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:81-85 COWIE VA; SINGH KR; WHEATER R; BIRD J THE FRAGILE-X SYNDROME IN TWIN SISTERS | 1 | 1 |
| 2086 | 15 | 22 | 718 1990 JOURNAL OF MENTAL DEFICIENCY RESEARCH 34:67-73 WEBB T; CRAWLEY P; BUNDEY S FOLATE TREATMENT OF A BOY WITH FRAGILE-X SYNDROME | 2 | 5 |
| 2087 | 3 | 7 | 719 1990 JOURNAL OF MENTAL DEFICIENCY RESEARCH 34:81-86 COLLACOTT RA; DUCKETT DP; MATHEWS D; WARRINGTON JS; YOUNG ID DOWNS-SYNDROME AND FRAGILE-X SYNDROME IN A SINGLE PATIENT | 0 | 0 |
| 2088 | 2 | 44 | 1265 1994 JOURNAL OF MOLECULAR BIOLOGY 243(2):143-151 SMITH SS; LAAYOUN A; LINGEMAN RG; BAKER DJ; RILEY J HYPERMETHYLATION OF TELOMERE-LIKE FOLDBACKS AT CODON-12 OF THE HUMAN C-HA-RAS GENE AND THE TRINUCLEOTIDE REPEAT OF THE FMR-1 GENE OF FRAGILE-X | 12 | 55 |
| 2089 | 11 | 67 | 1420 1995 JOURNAL OF MOLECULAR BIOLOGY 254(4):638-656 KETTANI A; KUMAR RA; PATEL DJ SOLUTION STRUCTURE OF A DNA QUADRUPLEX CONTAINING THE FRAGILE-X SYNDROME TRIPLET REPEAT | 15 | 98 |
| 2090 | 19 | 44 | 1553 1996 JOURNAL OF MOLECULAR BIOLOGY 258(4):614-626 Shimizu M; Gellibolian R; Oostra BA; Wells RD Cloning, characterization and properties of plasmids containing CGG triplet repeats from the FMR-1 gene | 14 | 49 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2091 | 0 | 28 | 1688 1997 JOURNAL OF MOLECULAR BIOLOGY 267(5):1171-1185 Tippin DB; Sundaralingam M Nine polymorphic crystal structures of d(CCGGGCCCGG), d(CCGGGCCm(5)CGG), d(Cm(5)CGGGCCm(5)CGG) and d(CCGGGCC(Br)(5)CGG) in three different conformations: Effects of spermine binding and methylation on the bending and condensation of A-DNA | 0 | 19 |
| 2092 | 10 | 40 | 1781 1998 JOURNAL OF MOLECULAR BIOLOGY 275(1):3-16 Darlow JM; Leach DRF Secondary structures in d(CGG) and d(CCG) repeat tracts | 8 | 44 |
| 2093 | 7 | 29 | 1782 1998 JOURNAL OF MOLECULAR BIOLOGY 275(1):17-23 Darlow JM; Leach DRF Evidence for two preferred hairpin folding patterns in d(CGG).d(CCG) repeat tracts in vivo | 3 | 21 |
| 2094 | 8 | 39 | 1783 1998 JOURNAL OF MOLECULAR BIOLOGY 283(1):111-120 Mariappan SVS; Silks LA; Bradbury EM; Gupta G Fragile X DNA triplet repeats, (GCC)(n), form hairpins with single hydrogen-bonded cytosine center dot cytosine mispairs at the CpG sites: Isotope-edited nuclear magnetic resonance spectroscopy on (GCC)(n) with selective (15)N4-labeled cytosine bases | 4 | 18 |
| 2095 | 41 | 65 | 2555 2004 JOURNAL OF MOLECULAR BIOLOGY 343(1):43-53 Menon RP; Gibson TJ; Pastore A The C terminus of fragile X mental retardation protein interacts with the multi-domain ran-binding protein in the microtubule-organising centre | 0 | 0 |
| 2096 | 5 | 6 | 2065 2000 JOURNAL OF MOLECULAR DIAGNOSTICS 2(3):128-131 Daly TM; Rafii A; Martin RA; Zehnbauer BA Novel polymorphism in the FMR1 gene resulting in a "pseudodeletion" of FMR1 in a commonly used fragile X assay | 0 | 0 |
| 2097 | 0 | 0 | 2556 2004 JOURNAL OF MOLECULAR DIAGNOSTICS 6(4):409-409 Lee JY; Zhang YT; Hopcus-Niccum D; Mulvihill JJ; Li SB A mosaicism of 45,X/46,XX/47,XXX uncovered by molecular fragile X testing | 0 | 0 |
| 2098 | 0 | 0 | 2557 2004 JOURNAL OF MOLECULAR DIAGNOSTICS 6(4):409-409 Williams J; Lyon E; Miller C; Mao R Chromosome aneuploidy detected by fragile X southern blot and PCR analysis | 0 | 0 |
| 2099 | 19 | 34 | 2558 2004 JOURNAL OF MOLECULAR HISTOLOGY 35(4):389-395 Reis SA; Willemsen R; van Unen L; Hoogeveen AT; Oostra BA Prospects of TAT-mediated protein therapy for fragile X syndrome | 0 | 0 |
| 2100 | 2 | 11 | 222 1984 JOURNAL OF NERVOUS AND MENTAL DISEASE 172(9):549-551 KERBESHIAN J; BURD L; MARTSOLF J A FAMILY WITH FRAGILE-X SYNDROME | 7 | 20 |