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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1001 | 0 | 0 | 1461 1996 BIOPHYSICAL JOURNAL 70(2):SU496-SU496 Chen X; Mariappan SVS; Ratliff R; Moyzis RK; Smith SS; Bradbury EM; Gupta G The formation and methylation of the ''slippage structures'' in vitro: The molecular basis of the fragile-X syndrome | 0 | 0 |
| 1002 | 18 | 62 | 2249 2003 BMC MOLECULAR BIOLOGY 4 Chandler SP; Kansagra P; Hirst MC Fragile X (CGG)(n) repeats induce a transcriptional repression in cis upon a linked promoter: Evidence for a chromatin mediated effect | 0 | 2 |
| 1003 | 2 | 6 | 1311 1995 BONE MARROW TRANSPLANTATION 16(4):625-626 MORTON J; ARNOLD L; FLETCHER B; MCCARTHY C; ROWELL J; DURRANT S ALLOGENEIC BMT FROM A DONOR WITH FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR EVALUATION | 0 | 0 |
| 1004 | 34 | 53 | 2000 2001 BRAIN 124:1610-1618 Eliez S; Blasey CM; Freund LS; Hastie T; Reiss AL Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome | 7 | 12 |
| 1005 | 28 | 62 | 2321 2004 BRAIN 127:591-601 Kogan CS; Boutet I; Cornish K; Zangenehpour S; Mullen KT; Holden JJA; Kaloustian VMD; Andermann E; Chaudhuri A Differential impact of the FMR1 gene on visual processing in fragile X syndrome | 0 | 0 |
| 1006 | 1 | 14 | 691 1990 BRAIN & DEVELOPMENT 12(1):128-130 WAHLSTROM J; WITTENGERSTROM I; MELLQUIST L; ANVRET M; ODEN A THE RETT SYNDROME RELATED TO FRAGILE-X(P22) IN CAFFEINE-INDUCED LYMPHOCYTE CULTURE | 0 | 13 |
| 1007 | 26 | 39 | 1312 1995 BRAIN & DEVELOPMENT 17(5):317-321 NANBA E; KOHNO Y; MATSUDA A; YANO M; SATO C; HASHIMOTO K; KOEDA T; YOSHINO K; KIMURA M; MAEOKA Y; YAMAMOTO T; MAEGAKI Y; EDA I; TAKESHITA K NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED JAPANESE MALES | 5 | 15 |
| 1008 | 4 | 5 | 1313 1995 BRAIN & DEVELOPMENT 17(5):322-322 NAKAHORI Y THE INCIDENCE OF THE FRAGILE-X SYNDROME IN JAPANESE - COMMENTARY ON NANBAS PAPER | 0 | 0 |
| 1009 | 4 | 7 | 1314 1995 BRAIN & DEVELOPMENT 17(5):323-323 KONDO I NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN JAPANESE MENTALLY-RETARDED MALES - COMMENT | 0 | 0 |
| 1010 | 5 | 9 | 2110 2002 BRAIN & DEVELOPMENT 24(8):766-769 Incorpora G; Sorge G; Sorge A; Pavone L Epilepsy in fragile X syndrome | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1011 | 0 | 0 | 1315 1995 BRAIN AND COGNITION 28(1):111-111 GRIGSBY J; KAYE K VARIABLE EXPRESSION OF DEVELOPMENTAL GERSTMANN SIGNS IN FRAGILE-X SYNDROME | 0 | 0 |
| 1012 | 0 | 0 | 1316 1995 BRAIN AND COGNITION 28(1):111-112 GRIGSBY J; KAYE K DISSOCIATIONS IN DEVELOPMENTAL DYSCALCULIA SECONDARY TO FRAGILE-X SYNDROME | 0 | 0 |
| 1013 | 11 | 52 | 1874 2000 BRAIN AND COGNITION 44(3):387-401 Munir F; Cornish KM; Wilding J Nature of the working memory deficit in Fragile-X syndrome | 5 | 6 |
| 1014 | 3 | 6 | 2322 2004 BRAIN AND COGNITION 54(3):235-239 Cornish K; Swainson R; Cunnington R; Wilding J; Morris P; Jackson G Do women with fragile X syndrome have problems in switching attention: Preliminary findings from ERP and fMRI | 0 | 0 |
| 1015 | 4 | 44 | 566 1988 BRAIN AND LANGUAGE 34(2):203-221 VILKMAN E; NIEMI J; IKONEN U FRAGILE-X SPEECH PHONOLOGY IN FINNISH | 4 | 5 |
| 1016 | 14 | 46 | 2111 2002 BRAIN RESEARCH 927(1):8-17 Nielsen DM; Derber WJ; McClellan DA; Crnic LS Alterations in the auditory startle response in Fmr1 targeted mutant mouse models of fragile X syndrome | 8 | 9 |
| 1017 | 12 | 41 | 2250 2003 BRAIN RESEARCH 971(1):83-89 Galvez R; Gopal AR; Greenough WT Somatosensory cortical barrel dendritic abnormalities in a mouse model of the fragile X mental retardation syndrome | 2 | 4 |
| 1018 | 25 | 36 | 2251 2003 BRAIN RESEARCH 972(1-2):9-15 Segal M; Kreher U; Greenberger V; Braun K Is fragile X mental retardation protein involved in activity-induced plasticity of dendritic spines? | 0 | 1 |
| 1019 | 28 | 88 | 2001 2001 BRAIN RESEARCH BULLETIN 56(3-4):367-373 Grabczyk E; Kumari D; Usdin K Fragile X syndrome and Friedreich's ataxia: Two different paradigms for repeat induced transcript insufficiency | 0 | 4 |
| 1020 | 42 | 85 | 2002 2001 BRAIN RESEARCH BULLETIN 56(3-4):375-382 Bardoni B; Schenck A; Mandel JL The Fragile X mental retardation protein | 4 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1021 | 32 | 62 | 2003 2001 BRAIN RESEARCH BULLETIN 56(3-4):383-387 Chiurazzi P; Neri G Pharmacological reactivation of inactive genes: The fragile X experience | 0 | 1 |
| 1022 | 20 | 38 | 2252 2003 BRAIN TOPOGRAPHY 15(3):165-171 Castren M; Paakkonen A; Tarkka IM; Ryynanen M; Partanen J Augmentation of auditory N1 in children with fragile X syndrome | 1 | 1 |
| 1023 | 25 | 35 | 1571 1997 BRAZILIAN JOURNAL OF GENETICS 20(4):731-739 Mingroni-Netto RC; Pavanello RCM; Otto PA; Vianna-Morgante AM Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families | 2 | 2 |
| 1024 | 2 | 14 | 692 1990 BRITISH DENTAL JOURNAL 168(4):160-162 NUNN JH; DURNING P FRAGILE-X (MARTIN BELL) SYNDROME AND DENTAL-CARE | 0 | 0 |
| 1025 | 4 | 9 | 628 1989 BRITISH HEART JOURNAL 61(3):289-291 SREERAM N; WREN C; BHATE M; ROBERTSON P; HUNTER S CARDIAC ABNORMALITIES IN THE FRAGILE X-SYNDROME | 6 | 9 |
| 1026 | 14 | 28 | 1203 1994 BRITISH JOURNAL OF CLINICAL PRACTICE 48(1):42-44 PATEL BD THE FRAGILE-X SYNDROME | 1 | 1 |
| 1027 | 0 | 1 | 1462 1996 BRITISH JOURNAL OF DEVELOPMENTAL PSYCHOLOGY 14:247-248 Happe F Behavior and development in fragile X syndrome - Dykens,EM, Hodapp,RM, Leckman,JF | 0 | 0 |
| 1028 | 1 | 8 | 1074 1993 BRITISH JOURNAL OF HAEMATOLOGY 85(2):415-416 VORST EJ; LEVENE NA; NISANI R; BERREBI A FRAGILE-X SYNDROME AND MYELODYSPLASIA DISCOVERED DURING PREGNANCY | 3 | 5 |
| 1029 | 6 | 13 | 693 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17 BUNDEY S FRAGILE-X SYNDROME | 1 | 1 |
| 1030 | 11 | 14 | 1875 2000 BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY 107(8):969-972 Kallinen J; Korhonen K; Kortelainen S; Heinonen S; Ryynanen M Pregnancy outcome in carriers of fragile X | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1031 | 2 | 11 | 116 1983 BRITISH JOURNAL OF PSYCHIATRY 143(SEP):256-260 GILLBERG C IDENTICAL TRIPLETS WITH INFANTILE-AUTISM AND THE FRAGILE-X SYNDROME | 20 | 38 |
| 1032 | 3 | 11 | 368 1986 BRITISH JOURNAL OF PSYCHIATRY 148:655-657 PRIMROSE DA; ELMATMATI R; BOYD E; GOSDEN C; NEWTON M PREVALENCE OF THE FRAGILE-X SYNDROME IN AN INSTITUTION FOR THE MENTALLY-HANDICAPPED | 16 | 22 |
| 1033 | 2 | 4 | 430 1987 BRITISH JOURNAL OF PSYCHIATRY 150:700-702 DEB S; COWIE VA; TIMBERLAKE C A CASE OF MOSAICISM WITH FRAGILE-X AND FRAGILE-XXY COMPONENTS | 5 | 5 |
| 1034 | 83 | 119 | 965 1992 BRITISH JOURNAL OF PSYCHIATRY 160:24-35 TURK J THE FRAGILE-X SYNDROME - ON THE WAY TO A BEHAVIORAL-PHENOTYPE | 24 | 45 |
| 1035 | 0 | 1 | 1317 1995 BRITISH JOURNAL OF PSYCHIATRY 166:688-688 COOKE LB BEHAVIOR AND DEVELOPMENT IN FRAGILE-X SYNDROME - DYKENS,E | 0 | 0 |
| 1036 | 17 | 31 | 431 1987 BRITISH MEDICAL JOURNAL 295(6598):564-565 KINNELL HG FRAGILE X-SYNDROME - AN IMPORTANT PREVENTABLE CAUSE OF MENTAL HANDICAP | 2 | 2 |
| 1037 | 1 | 4 | 432 1987 BRITISH MEDICAL JOURNAL 295(6603):922-922 MCKINLEY MJ; NICOLAIDES KH; KEARNEY LU; HERON O FRAGILE-X SYNDROME | 1 | 3 |
| 1038 | 1 | 2 | 837 1991 BRITISH MEDICAL JOURNAL 302(6789):1359-1359 CHARATAN F GENE FOR FRAGILE-X SYNDROME DISCOVERED | 0 | 0 |
| 1039 | 5 | 11 | 966 1992 BRITISH MEDICAL JOURNAL 305(6847):208-208 MOORE DWY NEW DEVELOPMENTS IN THE FRAGILE-X SYNDROME | 1 | 1 |
| 1040 | 0 | 1 | 1318 1995 BRITISH MEDICAL JOURNAL 310(6973):148-148 CRAFT N STUDY SUPPORTS SCREENING FOR THE FRAGILE-X-SYNDROME | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1041 | 0 | 0 | 1572 1997 BRITISH MEDICAL JOURNAL 315(7102):208-208 White C Screening for fragile X is cost effective and accurate | 0 | 0 |
| 1042 | 4 | 11 | 1573 1997 BRITISH MEDICAL JOURNAL 315(7117):1174-1175 Barnicoat A Screening for fragile X syndrome: a model for genetic disorders? | 1 | 4 |
| 1043 | 8 | 10 | 1574 1997 BRITISH MEDICAL JOURNAL 315(7117):1223-1226 Turner G; Robinson H; Wake S; Laing S; Partington M Case finding for the fragile X syndrome and its consequences | 5 | 9 |
| 1044 | 0 | 0 | 11 1981 BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE 165(9):1197-1206 LEJEUNE J MONOCARBONS METABOLISM AND FRAGILE-X SYNDROME | 22 | 30 |
| 1045 | 2 | 6 | 369 1986 BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE 102(12):1742-1745 ZAKHAROV AF; BEDELBAEVA KA; BARANOVSKAYA LI VARIABILITY OF FRAGILE X-CHROMOSOME EXPRESSION IN CONSECUTIVE CELL GENERATIONS | 0 | 0 |
| 1046 | 0 | 0 | 1204 1994 CANADIAN FAMILY PHYSICIAN 40:290-295 WIEBE E; WIEBE A FRAGILE-X SYNDROME | 0 | 1 |
| 1047 | 0 | 0 | 12 1981 CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES 8(2):191-191 SERGOVICH F; POZSONYI J; HINTON G RECENT ADVANCES IN MENTAL-RETARDATION THE FRAGILE X-CHROMOSOME | 1 | 0 |
| 1048 | 0 | 32 | 52 1982 CANADIAN MEDICAL ASSOCIATION JOURNAL 127(2):123-126 LARBRISSEAU A; JEAN P; MESSIER B; RICHER CL FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 6 | 9 |
| 1049 | 0 | 3 | 257 1985 CANADIAN MEDICAL ASSOCIATION JOURNAL 133(5):358-& SOUDEK D FRAGILE-X - A SYMPTOM OF THE DISEASE | 2 | 4 |
| 1050 | 5 | 31 | 567 1988 CANCER 62(11):2383-2386 CUNNINGHAM M; DICKERMAN JD FRAGILE-X SYNDROME AND ACUTE LYMPHOBLASTIC-LEUKEMIA | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1051 | 1 | 16 | 1205 1994 CANCER RESEARCH 54(19):5212-5216 LEE ST; MCGLENNEN RC; LITZ CE CLONAL DETERMINATION BY THE FRAGILE-X (FMR1) AND PHOSPHOGLYCERATE KINASE (PGK) GENES IN HEMATOLOGICAL MALIGNANCIES | 1 | 12 |
| 1052 | 9 | 34 | 838 1991 CELL 64(4):861-866 BELL MV; HIRST MC; NAKAHORI Y; MACKINNON RN; ROCHE A; FLINT TJ; JACOBS PA; TOMMERUP N; TRANEBJAERG L; FROSTERISKENIUS U; KERR B; TURNER G; LINDENBAUM RH; WINTER R; PEMBREY M; THIBODEAU S; DAVIES KE PHYSICAL MAPPING ACROSS THE FRAGILE-X - HYPERMETHYLATION AND CLINICAL EXPRESSION OF THE FRAGILE-X SYNDROME | 118 | 222 |
| 1053 | 11 | 40 | 839 1991 CELL 65(5):905-914 VERKERK AJMH; PIERETTI M; SUTCLIFFE JS; FU YH; KUHL DPA; PIZZUTI A; REINER O; RICHARDS S; VICTORIA MF; ZHANG FP; EUSSEN BE; VANOMMEN GJB; BLONDEN LAJ; RIGGINS GJ; CHASTAIN JL; KUNST CB; GALJAARD H; CASKEY CT; NELSON DL; OOSTRA BA; WARREN ST IDENTIFICATION OF A GENE (FMR-1) CONTAINING A CGG REPEAT COINCIDENT WITH A BREAKPOINT CLUSTER REGION EXHIBITING LENGTH VARIATION IN FRAGILE-X SYNDROME | 501 | 1246 |
| 1054 | 10 | 15 | 840 1991 CELL 66(4):817-822 PIERETTI M; ZHANG FP; FU YH; WARREN ST; OOSTRA BA; CASKEY CT; NELSON DL ABSENCE OF EXPRESSION OF THE FMR-1 GENE IN FRAGILE-X SYNDROME | 291 | 583 |
| 1055 | 12 | 23 | 841 1991 CELL 67(6):1047-1058 FU YH; KUHL DPA; PIZZUTI A; PIERETTI M; SUTCLIFFE JS; RICHARDS S; VERKERK AJMH; HOLDEN JJA; FENWICK RG; WARREN ST; OOSTRA BA; NELSON DL; CASKEY CT VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX | 368 | 933 |
| 1056 | 18 | 52 | 1075 1993 CELL 73(7):1403-1409 HANSEN RS; CANFIELD TK; LAMB MM; GARTLER SM; LAIRD CD ASSOCIATION OF FRAGILE-X SYNDROME WITH DELAYED REPLICATION OF THE FMR1 GENE | 23 | 121 |
| 1057 | 15 | 56 | 1076 1993 CELL 74(2):291-298 SIOMI H; SIOMI MC; NUSSBAUM RL; DREYFUSS G THE PROTEIN PRODUCT OF THE FRAGILE-X GENE, FMR1, HAS CHARACTERISTICS OF AN RNA-BINDING PROTEIN | 117 | 315 |
| 1058 | 15 | 39 | 1206 1994 CELL 77(1):33-39 SIOMI H; CHOI MY; SIOMI MC; NUSSBAUM RL; DREYFUSS G ESSENTIAL ROLE FOR KH DOMAINS IN RNA-BINDING - IMPAIRED RNA-BINDING BY A MUTATION IN THE KH DOMAIN OF FMR1 THAT CAUSES FRAGILE-X SYNDROME | 64 | 254 |
| 1059 | 20 | 53 | 1207 1994 CELL 77(6):853-861 KUNST CB; WARREN ST CRYPTIC AND POLAR VARIATION OF THE FRAGILE-X REPEAT COULD RESULT IN PREDISPOSING NORMAL ALLELES | 70 | 239 |
| 1060 | 22 | 52 | 1208 1994 CELL 78(1):23-33 BAKKER CE; VERHEIJ C; WILLEMSEN R; VANDERHELM R; OERLEMANS F; VERMEY M; BYGRAVE A; HOOGEVEEN AT; OOSTRA BA; REYNIERS E; DEBOULLE K; DHOOGE R; CRAS P; VANVELZEN D; NAGELS G; MARTIN JJ; DEDEYN PP; DARBY JK; WILLEMS PJ FMR1 KNOCKOUT MICE - A MODEL TO STUDY FRAGILE-X MENTAL-RETARDATION | 78 | 147 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1061 | 9 | 43 | 1463 1996 CELL 85(2):237-245 Musco G; Stier G; Joseph C; Morelli MAC; Nilges M; Gibson TJ; Pastore A Three-dimensional structure and stability of the KH domain: Molecular insights into the fragile X syndrome | 20 | 167 |
| 1062 | 11 | 59 | 1876 2000 CELL 100(3):323-332 Lewis HA; Musunuru K; Jensen KB; Edo C; Chen H; Darnell RB; Burley SK Sequence-specific RNA binding by a Nova KH domain: Implications for paraneoplastic disease and the fragile X syndrome | 7 | 86 |
| 1063 | 22 | 47 | 2004 2001 CELL 107(4):477-487 Brown V; Jin P; Ceman S; Darnell JC; O'Donnell WT; Tenenbaum SA; Jin XK; Feng Y; Wilkinson KD; Keene JD; Darnell RB; Warren ST Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome | 47 | 120 |
| 1064 | 17 | 85 | 2005 2001 CELL 107(4):489-499 Darnell JC; Jensen KB; Jin P; Brown V; Warren ST; Darnell RB Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function | 48 | 116 |
| 1065 | 16 | 17 | 2006 2001 CELL 107(5):555-557 Kaytor MD; Orr HT RNA targets of the fragile X protein | 5 | 13 |
| 1066 | 18 | 37 | 2007 2001 CELL 107(5):591-603 Zhang YQ; Bailey AM; Matthies HJG; Renden RB; Smith MA; Speese SD; Rubin GM; Broadie K Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function | 36 | 71 |
| 1067 | 34 | 62 | 2253 2003 CELL 112(3):317-327 Zalfa F; Giorgi M; Primerano B; Moro A; Di Penta A; Reis S; Oostra B; Bagni C The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at Synapses | 16 | 38 |
| 1068 | 6 | 21 | 2112 2002 CELLULAR & MOLECULAR BIOLOGY LETTERS 7(3):877-883 Denman RB Methylation of the arginine-glycine-rich region in the fragile X mental retardation protein FMRP differentially affects RNA binding | 2 | 4 |
| 1069 | 51 | 135 | 2323 2004 CELLULAR AND MOLECULAR LIFE SCIENCES 61(14):1714-1728 Denman RB; Dolzhanskaya N; Sung YJ Regulating a translational regulator: mechanisms cells use to control the activity of the fragile X mental retardation protein | 0 | 0 |
| 1070 | 21 | 34 | 2008 2001 CELLULAR AND MOLECULAR NEUROBIOLOGY 21(1):29-38 Castren M; Haapasalo A; Oostra BA; Castren E Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1071 | 22 | 79 | 1877 2000 CEREBRAL CORTEX 10(10):1038-1044 Irwin SA; Galvez R; Greenough WT Dendritic spine structural anomalies in fragile-X mental retardation syndrome | 27 | 45 |
| 1072 | 64 | 95 | 1464 1996 CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA 5(4):895-& Hagerman RJ Fragile X syndrome | 1 | 8 |
| 1073 | 16 | 37 | 370 1986 CHILD STUDY JOURNAL 16(4):285-296 BURD L; KERBESHIAN J FRAGILE X-SYNDROME - DEVELOPMENTAL ASPECTS | 0 | 1 |
| 1074 | 1 | 6 | 190 1984 CHINESE MEDICAL JOURNAL 97(11):861-864 XU BZ; REN S; XIAO GF; ZHOU XT A FRAGILE X SYNDROME FAMILY | 0 | 1 |
| 1075 | 0 | 3 | 1465 1996 CHINESE SCIENCE BULLETIN 41(5):436-437 Huang T; Shen Y; Fan Y; Wu GY Expression of two alternative splicing isoforms of fragile X gene in human placenta | 0 | 0 |
| 1076 | 3 | 18 | 1878 2000 CHINESE SCIENCE BULLETIN 45(6):516-520 Chen YT; Bardoni B; Yu M; Zhu N; Wu GY; Mandel JL; Shen Y Fragile X mental retardation protein interacts with TDG | 0 | 0 |
| 1077 | 2 | 19 | 568 1988 CHROMOSOMA 96(5):391-396 SAVAGE JRK; FITCHETT M THE BEHAVIOR OF FRAGILE-X AND OTHER ABERRATIONS DURING RECOVERY FROM LOW FOLATE CONDITIONS | 0 | 3 |
| 1078 | 2 | 29 | 569 1988 CHROMOSOMA 97(1):6-10 KEREM B; GOITEIN R; SCHAAP T CYTOLOGICAL EVIDENCE OF DEFECTIVE TEMPLATE IN THE FRAGILE X-CHROMOSOME | 2 | 5 |
| 1079 | 33 | 48 | 967 1992 CHROMOSOMA 101(7):381-387 OOSTRA BA; VERKERK AJMH THE FRAGILE X-SYNDROME - ISOLATION OF THE FMR-1 GENE AND CHARACTERIZATION OF THE FRAGILE-X MUTATION | 11 | 26 |
| 1080 | 0 | 0 | 258 1985 CLINICAL CHEMISTRY 31(6):1008-1009 THIBODEAU SN; FAULK KR; SMITH AC; BERRY R; HAGERMAN R THE USE OF RECOMBINANT DNA TECHNIQUES TO DOCUMENT THE TRANSMISSION OF FRAGILE-X SYNDROME THROUGH AN UNAFFECTED MALE CARRIER | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1081 | 0 | 0 | 371 1986 CLINICAL CHEMISTRY 32(6):1215-1215 THIBODEAU SN THE USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS (RFLP) TO DETERMINE THE CARRIER STATUS OF FRAGILE-X-SYNDROME | 0 | 0 |
| 1082 | 10 | 29 | 433 1987 CLINICAL CHEMISTRY 33(10):1726-1730 THIBODEAU SN USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS FOR DETECTING CARRIERS OF FRAGILE-X SYNDROME | 1 | 1 |
| 1083 | 0 | 0 | 1319 1995 CLINICAL CHEMISTRY 41(11):30-30 RADU DN; CHIANG CS RAPID, NONRADIOACTIVE SOUTHERN BLOT METHOD FOR DETECTING FRAGILE-X MUTATIONS | 0 | 0 |
| 1084 | 0 | 0 | 1466 1996 CLINICAL CHEMISTRY 42(6):441-441 Tsongalis GJ; Hodges KA; Adkins S; Silverman LM Chemiluminescent detection of the CGG trinucleotide repeat expansion in fragile X syndrome. | 0 | 0 |
| 1085 | 0 | 0 | 1467 1996 CLINICAL CHEMISTRY 42(11):7-7 Hamdan H; Bailey A; Martinez JJ; Fenwick R; Leon JA Improved amplification and automated detection of trinucleotide repeats in the diagnosis of fragile X syndrome. | 0 | 0 |
| 1086 | 0 | 0 | 1879 2000 CLINICAL CHEMISTRY 46(6):A206-A206 Boday A; Prusa R; Matoska V Radioactive PCR for the screening and diagnostics of fragile X chromosome syndrome - FRAXA. | 0 | 0 |
| 1087 | 0 | 18 | 372 1986 CLINICAL ENDOCRINOLOGY 24(3):327-333 OHARE JP; OBRIEN IAD; ARENDT J; ASTLEY P; RATCLIFFE W; ANDREWS H; WALTERS R; CORRALL RJM DOES MELATONIN DEFICIENCY CAUSE THE ENLARGED GENITALIA OF THE FRAGILE-X SYNDROME | 9 | 11 |
| 1088 | 0 | 19 | 13 1981 CLINICAL GENETICS 19(2):101-110 GUSTAVSON KH; HOLMGREN G; BLOMQUIST HK; MIKKELSEN M; NORDENSON I; POULSEN H; TOMMERUP N FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 2 SWEDISH FAMILIES | 28 | 42 |
| 1089 | 0 | 2 | 14 1981 CLINICAL GENETICS 19(2):140-141 SOUDEK D; GORZNY N NO FRAGILE X-CHROMOSOME IN NORMAL MEN | 1 | 3 |
| 1090 | 0 | 0 | 15 1981 CLINICAL GENETICS 19(6):493-493 NIELSEN KB; TOMMERUP N; POULSEN H; MIKKELSEN M DANISH FAMILIES WITH X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1091 | 2 | 4 | 16 1981 CLINICAL GENETICS 20(1):78-78 HOWARDPEEBLES PN FRAGILE-X CHROMOSOME IN NORMAL MALES | 4 | 7 |
| 1092 | 0 | 0 | 117 1983 CLINICAL GENETICS 23(3):216-216 MCDERMOTT A MORE ON THE FRAGILE-X, WITH PARTICULAR REFERENCE TO FIBROBLAST AND AMNIOTIC-FLUID CULTURE, AND X-INACTIVATION | 0 | 0 |
| 1093 | 1 | 1 | 118 1983 CLINICAL GENETICS 23(3):229-229 FONATSCH C FRAGILE X-CHROMOSOME IN FIBROBLASTS - LONGITUDINAL-STUDY ON TECHNICAL VARIATIONS | 3 | 3 |
| 1094 | 0 | 0 | 119 1983 CLINICAL GENETICS 23(3):232-232 VANDERHAGEN CB; ORSTAVIK KH; BAKKE J; BERG K MONOZYGOUS MALE TRIPLETS WITH MENTAL-RETARDATION AND A FRAGILE X-CHROMOSOME | 2 | 2 |
| 1095 | 0 | 0 | 120 1983 CLINICAL GENETICS 23(3):236-236 PAJARES IL; DELICADO A; GALLEGO A; CASTROVIEJO IP FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 6 SPANISH FAMILIES | 1 | 1 |
| 1096 | 0 | 0 | 121 1983 CLINICAL GENETICS 23(3):241-241 NIELSEN KB; TOMMERUP N; MIKKELSEN M CLINICAL AND CYTOGENETIC FINDINGS IN 26 MENTALLY-RETARDED MALES WITH THE FRAGILE-X | 1 | 1 |
| 1097 | 0 | 0 | 122 1983 CLINICAL GENETICS 23(3):250-251 TEJADA I; NICOLAS H; CHERUY C; BOUE J STUDY OF A LARGE SIBSHIP WITH MENTALLY-RETARDED MALES AND FEMALES CARRYING FRAGILE-X | 1 | 1 |
| 1098 | 0 | 0 | 123 1983 CLINICAL GENETICS 23(3):254-254 VEENEMA H; GERAEDTS JPM THE FRAGILE-X CHROMOSOME SEGREGATING IN A LARGE PEDIGREE | 2 | 2 |
| 1099 | 0 | 0 | 124 1983 CLINICAL GENETICS 23(3):255-255 VERSCHRAEGENSPAE MR; VANDENBOSSCHE H; MATTON MT APPROACH TO RELATIVES IN FRAGILE X-LINKED MENTAL-RETARDATION | 0 | 2 |
| 1100 | 5 | 14 | 125 1983 CLINICAL GENETICS 23(4):311-317 GARDNER RJM; SMART RD; CORNELL JM; MERCKEL LM; BEIGHTON P THE FRAGILE X-CHROMOSOME IN A LARGE INDIAN KINDRED | 17 | 20 |
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