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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by year, source, volume, issue, page.
Page 17: 1 (1) 2 (101) 3 (201) 4 (301) 5 (401) 6 (501) 7 (601) 8 (701) 9 (801) 10 (901) 11 (1001) 12 (1101) 13 (1201) 14 (1301) 15 (1401) 16 (1501) 17 (1601) 18 (1701) 19 (1801) 20 (1901) 21 (2001) 22 (2101) 23 (2201) 24 (2301)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1601 | 27 | 57 | 1601 1997 JOURNAL OF INHERITED METABOLIC DISEASE 20(2):139-151 Hoogeveen AT; Oostra BA The fragile X syndrome | 6 | 10 |
| 1602 | 0 | 0 | 1602 1997 JOURNAL OF MEDICAL GENETICS 34:SP69-SP69 Webb J; Murray A; Conway G; Jacobs P Premature ovarian failure and fragile X | 0 | 0 |
| 1603 | 0 | 0 | 1603 1997 JOURNAL OF MEDICAL GENETICS 34:505-505 Brady AF; Suri M; Emerson J; Bell J; Chotai K; Singh H; Pocha M; Brueton LA Unusual X chromosome inactivation resulting in fragile X phenotype in a girl with a deletion on (X)(q26q27) | 0 | 0 |
| 1604 | 0 | 0 | 1604 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 |
| 1605 | 0 | 0 | 1605 1997 JOURNAL OF MEDICAL GENETICS 34:539-539 Buckingham A; Bell JA; Payne SJ; Masters K; Emmerson J; Holder SE Recurrence of Turner's syndrome in a fragile-X family | 0 | 0 |
| 1606 | 0 | 0 | 1606 1997 JOURNAL OF MEDICAL GENETICS 34:541-541 Moore S; Dean JCS; Cole GF; Hamilton L; Kelly KF; Strain L; Warner J Fragile X Syndrome resulting from a deletion of the FMR1 gene | 0 | 0 |
| 1607 | 17 | 29 | 1607 1997 JOURNAL OF MEDICAL GENETICS 34(1):1-5 Morton JE; Bundey S; Webb TP; MacDonald F; Rindl PM; Bullock S Fragile X syndrome is less common than previously estimated | 25 | 45 |
| 1608 | 7 | 10 | 1608 1997 JOURNAL OF MEDICAL GENETICS 34(3):250-251 Willemsen R; Los F; Mohkamsing S; vandenOuweland A; Deelen W; Galjaard H; Oostra B Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A new appraisal | 10 | 12 |
| 1609 | 0 | 1 | 1609 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 |
| 1610 | 1 | 2 | 1610 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1611 | 12 | 38 | 1611 1997 JOURNAL OF MEDICAL GENETICS 34(11):907-911 vanRijn MA; deVries BBA; Tibben A; vandenOuweland AMW; Halley DJJ; Niermeijer MF DNA testing for fragile X syndrome: implications for parents and family | 3 | 4 |
| 1612 | 10 | 15 | 1612 1997 JOURNAL OF MEDICAL GENETICS 34(11):924-926 Losekoot M; Hoogendoorn E; Olmer R; Jansen CCAM; Oosterwijk JC; vandenOuweland AMW; Halley DJJ; Warren ST; Willemsen R; Oostra BA; Bakker E 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 |
| 1613 | 23 | 59 | 1613 1997 JOURNAL OF NEUROSCIENCE 17(5):1539-1547 Feng Y; Gutekunst CA; Eberhart DE; Yi H; Warren ST; Hersch SM Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodendritic ribosomes | 71 | 131 |
| 1614 | 5 | 12 | 1614 1997 JOURNAL OF SPECIAL EDUCATION 31(3):362-376 Powell L; Houghton S; Douglas G Comparison of etiology-specific cognitive functioning profiles for individuals with fragile X and individuals with Down syndrome | 2 | 4 |
| 1615 | 7 | 35 | 1615 1997 JOURNAL OF THEORETICAL BIOLOGY 188(1):53-67 Bat O; Kimmel M; Axelrod DE Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease | 1 | 4 |
| 1616 | 42 | 92 | 1616 1997 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 3(4):313-322 Abbeduto L; Hagerman RJ Language and communication in fragile X syndrome | 10 | 14 |
| 1617 | 24 | 47 | 1617 1997 MOLECULAR CELL 1(1):109-118 Feng Y; Absher D; Eberhart DE; Brown V; Malter HE; Warren ST FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association | 65 | 114 |
| 1618 | 7 | 20 | 1618 1997 MOLECULAR DIAGNOSIS 2(4):259-269 Hamdan H; Tynan JA; Fenwick RA; Leon JA Automated detection of trinucleotide repeats in fragile X syndrome | 4 | 6 |
| 1619 | 22 | 42 | 1619 1997 NATURE GENETICS 15(2):165-169 Malter HE; Iber JC; Willemsen R; deGraaff E; Tarleton JC; Leisti J; Warren ST; Oostra BA Characterization of the full fragile X syndrome mutation in fetal gametes | 45 | 84 |
| 1620 | 7 | 34 | 1620 1997 NATURE STRUCTURAL BIOLOGY 4(9):712-716 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; Nilges M; Pastore A The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome | 5 | 40 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1621 | 1 | 1 | 1621 1997 NATURE STRUCTURAL BIOLOGY 4(10):840-840 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; Nilges M; Pastore A The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome (vol 4, pg 712, 1997) | 0 | 0 |
| 1622 | 0 | 0 | 1622 1997 NEUROLOGY 48(3):5062-5062 Mostofsky SH; Mazzocco MM; Aakalu G; Warsofsky IS; Denckla MB; Reiss AL Aberrant posterior vermis size in fragile X syndrome: Correlation with neurocognitive performance | 0 | 0 |
| 1623 | 3 | 10 | 1623 1997 PEDIATRICS 99(5):753-753 Hagerman R Fragile X: Treatment of hyperactivity | 0 | 1 |
| 1624 | 21 | 69 | 1624 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(9):4587-4592 Hansen RS; Canfield TK; Fjeld AD; Mumm S; Laird CD; Gartler SM A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication | 8 | 41 |
| 1625 | 16 | 58 | 1625 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(10):5395-5400 Weiler IJ; Irwin SA; Klintsova AY; Spencer CM; Brazelton AD; Miyashiro K; Comery TA; Patel B; Eberwine J; Greenough WT Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation | 86 | 174 |
| 1626 | 10 | 29 | 1626 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(10):5401-5404 Comery TA; Harris JB; Willems PJ; Oostra BA; Irwin SA; Weiler IJ; Greenough WT Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits | 111 | 201 |
| 1627 | 23 | 44 | 1627 1997 PSYCHIATRIC GENETICS 7(3):115-119 ODwyer J; Holmes J; Mueller R; Taylor G The prevalence of Fragile-X syndrome in an institution for people with learning disability | 1 | 2 |
| 1628 | 2 | 54 | 1628 1997 PSYCHIATRY RESEARCH-NEUROIMAGING 75(1):31-48 Kates WR; Abrams MT; Kaufmann WE; Breiter SN; Reiss AL Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome | 16 | 53 |
| 1629 | 29 | 49 | 1629 1997 REVISTA DE NEUROLOGIA 25(143):1068-1071 EstevezGonzalez A; Roig C; Piles S; Pineda M; GarciaSanchez C Fragile-X syndrome and mental retardation | 0 | 0 |
| 1630 | 4 | 10 | 1630 1997 SOUTH AFRICAN MEDICAL JOURNAL 87(4):418-420 Goldman A; Krause A; Jenkins T Fragile X syndrome occurs in the South African black population | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1631 | 76 | 123 | 1631 1997 WESTERN JOURNAL OF MEDICINE 166(2):129-137 Hagerman RJ Fragile X syndrome - Molecular and clinical insights and treatment issues | 5 | 8 |
| 1632 | 8 | 22 | 1632 1997 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 97(8):33-37 Gorbachevskaya NL; Denisova LV Bioelectric brain activity in patients with syndrome of fragile X-chromosome and in their mothers | 0 | 1 |
| 1633 | 20 | 33 | 1633 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 79(3):200-204 Bonaventure G; Torrado M; Barreiro C; Chertkoff L Fragile X founder effects in Argentina | 0 | 2 |
| 1634 | 0 | 0 | 1634 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 81(6):452-453 Oostra BA Fragile X syndrome is caused by a fragile gene. | 0 | 0 |
| 1635 | 0 | 0 | 1635 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 81(6):552-552 von Gontard A; Backes M; Schreck J; Genc B; Doerfler W Behavioural phenotype of the fragile-X-syndrome. | 0 | 0 |
| 1636 | 0 | 0 | 1636 1998 AMERICAN JOURNAL OF PATHOLOGY 153(5):1651-1651 Wages J; Bloch W; Burman R; Popovich B; Kruckeberg KE; Tester DJ; Snow K Size accuracy in a fragile X size-polymorphism assay | 0 | 0 |
| 1637 | 13 | 23 | 1637 1998 AMERICAN JOURNAL ON MENTAL RETARDATION 103(1):29-39 Bailey DB; Hatton DD; Skinner M Early developmental trajectories of males with fragile X syndrome | 28 | 30 |
| 1638 | 19 | 30 | 1638 1998 ANNALS OF HUMAN GENETICS 62:337-347 Huggins RM; Loesch DZ; Sherman SL A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation | 1 | 2 |
| 1639 | 2 | 5 | 1639 1998 ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE 152(1):89-90 Tsuchiya KD; Forsythe M; Robin NH; Tunnessen WW Picture of the month - Fragile X syndrome | 0 | 0 |
| 1640 | 14 | 24 | 1640 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):9-17 Felix TM; De Pina-Neto JM Fragile X syndrome - Clinical and cytogenetic studies | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1641 | 12 | 30 | 1641 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):18-23 Guerreiro MM; Camargo EE; Kato M; Marques-De-Faria AP; Ciasca SM; Guerreiro CAM; Netto JRM; Moura-Ribeiro MVL Fragile X syndrome - Clinical, electroencephalographic and neuroimaging characteristics | 7 | 13 |
| 1642 | 12 | 28 | 1642 1998 CLINICAL GENETICS 53(3):179-183 Chan SY; Wong V DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome | 2 | 5 |
| 1643 | 8 | 10 | 1643 1998 CLINICAL GENETICS 53(3):200-201 Mornet E; Chateau C; Simon-Bouy B; Serre JL The intermediate alleles of the fragile X CGG repeat in patients with mental retardation | 3 | 6 |
| 1644 | 18 | 30 | 1644 1998 CLINICAL GENETICS 54(4):309-314 Russo S; Briscioli V; Cogliati F; Macchi M; Lalatta F; Larizza L An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutation | 0 | 1 |
| 1645 | 0 | 2 | 1645 1998 CLINICAL GENETICS 54(4):365-365 Toro-Sola MA Fragile X and Rett syndromes in Puerto Rico | 0 | 0 |
| 1646 | 7 | 12 | 1646 1998 CLINICAL GENETICS 54(4):366-367 Vatta S; Cigui I; Demori E; Morgutti M; Pecile V; Benussi DG; Serra C; Amoroso A Fragile X syndrome, mental retardation and macroorchidism | 3 | 3 |
| 1647 | 29 | 107 | 1647 1998 CURRENT OPINION IN GENETICS & DEVELOPMENT 8(2):245-253 Tapscott SJ; Klesert TR; Widrow RJ; Stoger R; Laird CD Fragile-X syndrome and myotonic dystrophy: parallels and paradoxes | 0 | 10 |
| 1648 | 12 | 14 | 1648 1998 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 40(1):62-64 Gringras P; Barnicoat A Retesting for fragile X syndrome in cytogenetically normal males | 1 | 3 |
| 1649 | 8 | 26 | 1649 1998 EPIGENETICS 214:280-290 Laird; Pillus; Hirst; Bestor; Jaenisch; Wilkins; Gasser; Wolffe; Francke; Bird; Riggs; Horz Rules of DNA methylation in humans inferred from the fragile X gene, FMR1 - Final general discussion | 0 | 0 |
| 1650 | 0 | 0 | 1650 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:44-44 Tamanini F; van Unen L; Bontekoe C; Bakker; Willemsen R; Oostra BA; Hoogeveen AT Oligomerization and intracellular transport of the Fragile X Mental Retardation Protein | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1651 | 0 | 0 | 1651 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:63-63 Weinhausel A; Skarits C; Wolschek M; Haas OA Diagnostic evaluation of the fragile X syndrome with methylation-sensitive PCR (MS-PCR) | 0 | 0 |
| 1652 | 0 | 0 | 1652 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:107-107 Peixoto A; Santos R; Seruca R; Amorim A; Castedo S Haplotype analysis in fragile X and normal Portuguese populations | 0 | 0 |
| 1653 | 0 | 0 | 1653 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:116-116 Duran M; Valverde L; Molina M; Onaindia ML; Tejada MI Carrier screening for fragile X by PCR in females: comparison with obligated carriers | 0 | 0 |
| 1654 | 0 | 0 | 1654 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:144-144 Patsalis P; Sismani C; Hettinger JA; Boumba I; Georgiou I; Stylianidou G; Anastasiadou V; Koukoulli R; Pagoulatos G; Syrrou M Population-based molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes: incidence, genetic variation and stability | 0 | 0 |
| 1655 | 0 | 0 | 1655 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:159-159 Strelnikov V; Nemstova M; Demina N; Galkina V; Kuleshov N; Zaletayev D DNA testing for fragile X syndrome | 0 | 0 |
| 1656 | 23 | 30 | 1656 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6(5):518-522 Peixoto A; dos Santos MR; Seruca R; Amorim A; Castedo S Analysis of FMR1 and flanking microsatellite markers in normal and fragile X chromosomes in Portugal: evidence for a "protector" haplotype | 1 | 1 |
| 1657 | 0 | 0 | 1657 1998 FASEB JOURNAL 12(8):A1322-A1322 Warren ST The molecular basis of Fragile X syndrome | 0 | 0 |
| 1658 | 0 | 10 | 1658 1998 GENERAL HOSPITAL PSYCHIATRY 20(2):126-127 Silva JA; Ferrari MM; Leong GB Erotomania in a case of fragile-X syndrome | 0 | 1 |
| 1659 | 4 | 7 | 1659 1998 HUMAN GENETICS 102(1):54-56 Storm K; Handig I; Reyniers E; Oostra BA; Kooy RF; Willems PJ Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome | 0 | 1 |
| 1660 | 21 | 41 | 1660 1998 HUMAN GENETICS 102(4):440-445 Gronskov K; Hallberg A; Brondum-Nielsen K Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations | 3 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1661 | 0 | 0 | 1661 1998 HUMAN GENETICS 103(3):366-366 Gronskov K; Brondum-Nielsen K Regarding the letter from Dr. Stephen T. Warren of the Emory University School of Medicine concerning our article "Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations" | 0 | 0 |
| 1662 | 19 | 29 | 1662 1998 HUMAN HEREDITY 48(5):256-265 Hecimovic S; Barisic I; Pavelic K DNA analysis of the fragile X syndrome in an at risk pediatric population in Croatia: Simple clinical preselection criteria can considerably improve the cost-effectiveness of fragile X screening studies | 3 | 5 |
| 1663 | 13 | 28 | 1663 1998 HUMAN MOLECULAR GENETICS 7(1):109-113 Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G In vitro reactivation of the FMR1 gene involved in fragile X syndrome | 21 | 47 |
| 1664 | 13 | 29 | 1664 1998 HUMAN MOLECULAR GENETICS 7(13):2121-2128 Khandjian EW; Bardoni B; Corbin F; Sittler A; Giroux S; Heitz D; Tremblay S; Pinset C; Montarras D; Rousseau F; Mandel JL Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis | 17 | 27 |
| 1665 | 2 | 4 | 1665 1998 HUMAN MUTATION 12(6):431-431 Vincent JB; Gurling HMD Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome | 3 | 5 |
| 1666 | 0 | 0 | 1666 1998 HUMAN MUTATION 12(6):432-432 Wang YC; Li SY Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome - Response | 0 | 1 |
| 1667 | 18 | 36 | 1667 1998 HUMAN REPRODUCTION 13(5):1184-1187 Conway GS; Payne NN; Webb J; Murray A; Jacobs PA Fragile X premutation screening in women with premature ovarian failure | 8 | 31 |
| 1668 | 14 | 22 | 1668 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 107:29-36 Baskaran S; Naseerullah MK; Manjunatha KR; Chetan GK; Arthi R; Rao GVB; Girimaji SR; Srinath S; Sheshadri S; Devi RR; Brahmachari V Triplet repeat polymorphism & fragile X syndrome in the Indian context | 2 | 6 |
| 1669 | 14 | 26 | 1669 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 108:12-16 Jain U; Verma IC; Kapoor AK Prevalence of fragile X(A) syndrome in mentally retarded children at a genetics referral centre in Delhi, India | 2 | 3 |
| 1670 | 13 | 42 | 1670 1998 JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES 11(3):175-191 Turk J Fragile X syndrome and attentional deficits | 11 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1671 | 10 | 39 | 1671 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(4):321-328 Mazzocco MMM; Pulsifer M; Fiumara A; Cocuzza M; Nigro F; Incorpora G; Barone R Brief report: Autistic behaviors among children with fragile X or Rett syndrome: Implications for the classification of pervasive developmental disorder | 4 | 8 |
| 1672 | 53 | 104 | 1672 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(5):393-405 Feinstein C; Reiss AL Autism: The point of view from fragile X studies | 15 | 42 |
| 1673 | 17 | 28 | 1673 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):499-508 Bailey DB; Mesibov GB; Hatton DD; Clark RD; Roberts JE; Mayhew L Autistic behavior in young boys with fragile X syndrome | 29 | 36 |
| 1674 | 12 | 36 | 1674 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 | 8 | 11 |
| 1675 | 10 | 37 | 1675 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(25):15521-15527 Brown V; Small K; Lakkis L; Feng Y; Gunter C; Wilkinson KD; Warren ST Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein | 36 | 62 |
| 1676 | 6 | 30 | 1676 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 | 2 | 6 |
| 1677 | 3 | 66 | 1677 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 | 13 |
| 1678 | 10 | 33 | 1678 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 |
| 1679 | 7 | 40 | 1679 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 |
| 1680 | 46 | 75 | 1680 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1681 | 0 | 0 | 1681 1998 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 19(5):381-381 Taylor RJ; Scharfenaker S; O'Connor R; Lampe M; Kovach T; Hills J; Tassone F; Taylor AK; Hagerman RJ Severe language impairment in fragile X syndrome: Clinical correlates and treatment approaches | 0 | 0 |
| 1682 | 24 | 41 | 1682 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:81-89 Elbaz A; Suedois J; Duquesnoy M; Beldjord C; Berchel C; Merault G Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies | 5 | 8 |
| 1683 | 17 | 41 | 1683 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:490-499 Turk J; Cornish K Face recognition and emotion perception in boys with fragile-X syndrome | 9 | 15 |
| 1684 | 0 | 0 | 1684 1998 JOURNAL OF INVESTIGATIVE MEDICINE 46(1):87A-87A Miller LJ; McIntosh D; McGrath J; Shyu V; Lampe M; Taylor AK; Tassone F; Neitzel K; Stackhouse T; Hagerman RJ Electrodermal responses to sensory stimuli in individuals with fragile X sydrome. | 0 | 0 |
| 1685 | 27 | 51 | 1685 1998 JOURNAL OF MEDICAL GENETICS 35(2):103-111 Wohrle D; Salat U; Glaser D; Mucke J; Meisel-Stosiek M; Schindler D; Vogel W; Steinbach P Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats | 15 | 28 |
| 1686 | 134 | 197 | 1686 1998 JOURNAL OF MEDICAL GENETICS 35(7):579-589 de Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF The fragile X syndrome | 28 | 50 |
| 1687 | 5 | 8 | 1687 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 |
| 1688 | 6 | 39 | 1688 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 | 16 |
| 1689 | 14 | 40 | 1689 1998 JOURNAL OF NEUROSCIENCE RESEARCH 51(1):41-48 Berry-Kravis E; Ciurlionis R Overexpression of fragile X gene (FMR-1) transcripts increases cAMP production in neural cells | 0 | 1 |
| 1690 | 20 | 36 | 1690 1998 JOURNAL OF PEDIATRICS 133(3):363-365 Meyer GA; Blum NJ; Hitchcock W; Fortina P Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1691 | 0 | 0 | 1691 1998 MOLECULAR BIOLOGY OF THE CELL 9:185A-185A Lichtenstein H; Tartakoff A Nuclear export of the Fragile X gene product, FMRP | 0 | 0 |
| 1692 | 1 | 1 | 1692 1998 MOLECULAR DIAGNOSIS 3(4):249-249 Hamdan H; Tynan JA; Fenwick RA; Leon JA Automated detection of trinucleotide repeats in Fragile X syndrome (vol 2, pg 259, 1997) | 0 | 0 |
| 1693 | 18 | 63 | 1693 1998 NEUROLOGY 50(1):121-130 Mostofsky SH; Mazzocco MMM; Aakalu G; Warsofsky IS; Denckla MB; Reiss AL Decreased cerebellar posterior vermis size in fragile X syndrome - Correlation with neurocognitive performance | 18 | 44 |
| 1694 | 0 | 0 | 1694 1998 NEUROLOGY 50(4):A86-A86 Mostofsky SH; Reiss AL; Freund L Examination of posterior vermis size in young males with fragile X syndrome | 0 | 0 |
| 1695 | 17 | 36 | 1695 1998 NEUROPSYCHOLOGIA 36(11):1239-1246 Cornish KM; Munir F; Cross G The nature of the spatial deficit in young females with Fragile-X syndrome: A neuropsychological and molecular perspective | 10 | 14 |
| 1696 | 6 | 11 | 1696 1998 NEUROREPORT 9(3):477-481 Steward O; Bakker CE; Willems PJ; Oostra BA No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome | 10 | 16 |
| 1697 | 19 | 33 | 1697 1998 OPTOMETRY AND VISION SCIENCE 75(12):856-859 Kranjc BS; Brezigar A; Peterlin B Bilateral macular dysplasia in fragile X syndrome | 0 | 0 |
| 1698 | 29 | 41 | 1698 1998 REVISTA MEDICA DE CHILE 126(8):911-918 Jara L; Lopez M; Mellado C; Aspillaga M; Avendano I; Blanco R Clinical and metabolic screening for fragile X syndrome in 300 patients with unspecific mental retardation | 0 | 0 |
| 1699 | 9 | 25 | 1699 1998 REVISTA MEDICA DE CHILE 126(12):1447-1454 Aspillaga M; Jara L; Avendano I; Lopez M Fragile X syndrome. Clinical analysis of 300 Chilean patients with unspecific mental retardation | 1 | 1 |
| 1700 | 2 | 13 | 1700 1998 STEROIDS 63(1):2-4 Joseph DR The rat androgen-binding protein (ABP/SHBG) gene contains triplet repeats similar to unstable triplets: Evidence that the ABP/SHBG and the fragile X-related 2 genes overlap | 0 | 8 |
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