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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2001 | 0 | 0 | 1549 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A389-A389 Ye LL; Ju W; Xu WM; Schupf N; Jenkins EC; Brown WT; Zhong N Distribution of apolipoprotein E genotypes in the fragile X syndrome, Batten disease, and Down syndrome populations. | 0 | 0 |
| 2002 | 0 | 0 | 1550 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A407-A407 Sucharov CC; Varandas FR; Rondinelli E; Carakushansky G; Moura-Neto RS Establishment of a differential diagnostic of patients with Mental Retardation based on Southern-blot and PCR considering the frequency of Fragile X trinucleotide repeats from normal population in Rio de Janeiro, Brazil. | 0 | 0 |
| 2003 | 0 | 0 | 1551 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A407-A407 Taylor AK; Tassone F; Staley-Gane L; Hagerman RJ Identical premutation size in multiple tissues of a male fragile X carrier. | 0 | 0 |
| 2004 | 12 | 39 | 1558 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 74(2):167-171 Miezejeski CM; Heaney G; Belser R; Brown WT; Jenkins EC; Sersen EA Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation | 0 | 0 |
| 2005 | 0 | 0 | 1559 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 74(6):568-568 Bleiweiss H; Pollini A; Goldemberg A; Schuarzberg C; Staszauer M; Bleiweiss D Treatment of patients with fragile X syndrome and psychiatric abnormalities. | 0 | 0 |
| 2006 | 0 | 0 | 1560 1997 AMERICAN JOURNAL OF PATHOLOGY 151(5):G3-G3 Shrimpton AE; Hicks K; Lamberson CM Fragile X syndrome molecular detection. | 0 | 0 |
| 2007 | 2 | 15 | 1562 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):457-460 BillonGalland IO The fragile X syndrome and its clinical psychotic expression | 0 | 0 |
| 2008 | 0 | 0 | 1563 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):460-460 Koupernik; Doutheau; Rapporteur The fragile X syndrome and its clinical psychotic expression - Discussion | 0 | 0 |
| 2009 | 0 | 0 | 1566 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Mornet E Fragile X syndrome - Response | 0 | 0 |
| 2010 | 1 | 1 | 1567 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Beauvais P Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2011 | 1 | 1 | 1570 1997 ARCHIVES OF MEDICAL RESEARCH 28(1):149-149 Rivera H Fragile X studies and authorship (vol 27, pg 587, 1996) | 0 | 0 |
| 2012 | 0 | 0 | 1572 1997 BRITISH MEDICAL JOURNAL 315(7102):208-208 White C Screening for fragile X is cost effective and accurate | 0 | 0 |
| 2013 | 0 | 0 | 1580 1997 CYTOGENETICS AND CELL GENETICS 77(1-2):P250-P250 Malarchuk S; Li S; Wertelecki W; Bychkova A; Livshits L Analysis of patients with fragile X syndrome in Ukraine. | 0 | 0 |
| 2014 | 0 | 0 | 1581 1997 CYTOGENETICS AND CELL GENETICS 77(1-2):P287-P287 Tengstrom C; Ikonen A; Kaski M; Autio S High resolution banding and fragile X - screening in persons with mild mental retardation. | 0 | 0 |
| 2015 | 1 | 1 | 1583 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(5):304-304 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; Naeem R Five-year experience with Fragile X-testing - Setting laboratory standards of practice and a cost-effective protocol (vol 6, pg 161, 1997) | 0 | 0 |
| 2016 | 26 | 48 | 1585 1997 FOLIA HISTOCHEMICA ET CYTOBIOLOGICA 35(3):135-141 Szot M The fragile X syndrome | 0 | 0 |
| 2017 | 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 |
| 2018 | 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 |
| 2019 | 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 |
| 2020 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2021 | 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 |
| 2022 | 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 |
| 2023 | 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 |
| 2024 | 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 |
| 2025 | 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 |
| 2026 | 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 |
| 2027 | 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 |
| 2028 | 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 |
| 2029 | 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 |
| 2030 | 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 |
| 2031 | 0 | 2 | 1645 1998 CLINICAL GENETICS 54(4):365-365 Toro-Sola MA Fragile X and Rett syndromes in Puerto Rico | 0 | 0 |
| 2032 | 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 |
| 2033 | 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 |
| 2034 | 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 |
| 2035 | 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 |
| 2036 | 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 |
| 2037 | 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 |
| 2038 | 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 |
| 2039 | 0 | 0 | 1657 1998 FASEB JOURNAL 12(8):A1322-A1322 Warren ST The molecular basis of Fragile X syndrome | 0 | 0 |
| 2040 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2041 | 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 |
| 2042 | 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 |
| 2043 | 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 |
| 2044 | 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 |
| 2045 | 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 |
| 2046 | 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 |
| 2047 | 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 |
| 2048 | 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 |
| 2049 | 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 |
| 2050 | 71 | 144 | 1701 1998 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 98(9):54-63 Vorsanova SG; Vekhova NV; Demidova IA; Yurov YB Syndrome of mental retardation, linked with fragile X-chromosome: problems of diagnostics and inheritance | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2051 | 0 | 0 | 1704 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A29-A29 Ceman S; Brown V; Warren ST Isolation of an FMRP-associated mRNP and the identification of nucleolin and the fragile X-related proteins as components of the complex. | 0 | 0 |
| 2052 | 0 | 0 | 1705 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A49-A49 Drasinover V; Ehrlich S; Magal N; Taub E; Libman V; Shohat T; Shohat M Increased transmission of the premutated allele compared to the normal allele in female carriers of the fragile X syndrome. | 0 | 0 |
| 2053 | 0 | 0 | 1706 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A68-A68 Fisch GS; Howard-Peebles PN; Carpenter N; Tarleton J; Simensen R; Holden JJA Age-related features of genetic mutations producing cognitive impairment: the Fragile X mutation, NF1, and Williams Syndrome. | 0 | 0 |
| 2054 | 0 | 0 | 1707 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A103-A103 Brown WT; Rabe A; Durnas R; Haubenstock H; Dobkin C FMR1 knockout mouse shows a strain-specific severe learning impairment: A robust model for the fragile X syndrome. | 0 | 0 |
| 2055 | 0 | 0 | 1708 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A105-A105 Kenneson A; Hagedorn CH; Warren ST Quantitative studies of the fragile X mental retardation 1 (FMR1) gene product, FMRP. | 0 | 0 |
| 2056 | 0 | 0 | 1709 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A145-A145 Chernoff EJ; Nunes M; White B; McClellan J; Coll E; Maggio K; Levin S Fragile X premutation status in a male with mental retardation. | 0 | 0 |
| 2057 | 0 | 0 | 1710 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A165-A165 Iqbal MA; Sakati N; Nester A; Ozand P Cytogenetic diagnosis of fragile X syndrome a study of 305 suspected cases in Saudi Arabia. | 0 | 0 |
| 2058 | 0 | 0 | 1711 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A214-A214 Falik-Zaccai TC; Shachak E; Borochowitz Z; Magal N; Zatz S; Shochat M; Ziv H; Navon R; Ligum C; Shomrat R Fragile X syndrome: Population carrier screening and implication for prenatal diagnosis. | 0 | 0 |
| 2059 | 0 | 0 | 1712 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A266-A266 Burman RW; Popovich BW; Yates PA; Jacky PB; Schnell JL; Turker MS Fully expanded fragile X CGG repeats exhibit a length-and differentiation-dependent instability in cell hybrids that is independent of DNA methylation. | 0 | 0 |
| 2060 | 0 | 0 | 1713 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A268-A268 Crawford DC; Schwartz CE; Warren ST; Sherman SL Novel repeat structures identified in African-Americans represent a new mechanism leading to fragile X CGG repeat instability. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2061 | 0 | 0 | 1714 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A270-A270 El-Hazmi MF Fragile X mental retardation in syndrome in Saudi Arabia. | 0 | 0 |
| 2062 | 0 | 0 | 1715 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A279-A279 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Macpherson J; Brondum-Nielsen K; Hasholt L; Norgarrd-Pedersen B; Vuust J Haplotype and AGG-interspersion analysis of FMR1(CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles | 0 | 0 |
| 2063 | 0 | 0 | 1717 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A471-A471 Ventura KA; Fraer LM; Smith EE; Merrill AE; Treat KJ; Wang Z; Allitto BA; DeMarchi JM; Hogge WA Transmission on a fragile X full mutation through a normal transmitting male. | 0 | 0 |
| 2064 | 0 | 0 | 1718 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A474-A474 Lazarou LP; Warburton S; Roberts CE; Lindley VH; Bartlett S; Hughes HE; Meredith L; Ravine D Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male. | 0 | 0 |
| 2065 | 0 | 0 | 1719 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A493-A493 Tassone F; Hagerman RJ; Taylor AK; Mills JB; Wood S; Gane LW; Hagerman PJ FMR1 mRNA expression levels in fragile X. | 0 | 0 |
| 2066 | 4 | 13 | 1730 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):296-297 Ferri R; Del Gracco S; Elia M; Musumeci SA; Pettinato S Heart rate variability and autonomic function during sleep in fragile X syndrome | 0 | 0 |
| 2067 | 3 | 13 | 1759 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):309-310 Zhong N; Ju WN; Brown WT; Ye LL; Jenkins EC; Schupf N Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease | 0 | 0 |
| 2068 | 0 | 0 | 1768 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-767 Lesniak-Karpiak K; Mazzocco MM; Lanham DC; Denckla MB Behavioral assessment of social skills in children with Turner syndrome or Fragile X. | 0 | 0 |
| 2069 | 10 | 18 | 1770 1999 AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY 33(3):436-440 Al-Semaan Y; Malla AK; Lazosky A Schizoaffective disorder in a fragile-X carrier | 0 | 0 |
| 2070 | 0 | 0 | 1777 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):137-138 Arrieta I; Criado B; Martinez B; Telez M; Fiores P; Ortega B; Penagarikano O; Lostao CM Molecular and cytogenetic analysis of the fragile X syndrome in a sample from Basque Country: are the Basques a population with a low risk of developing the syndrome? | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2071 | 0 | 0 | 1778 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):165-165 Sofocleous C; Mavrou A; Fryssira H; Kolialexi A; Tsenghi C; Metaxotou C FMRP (Fragile X Mental Retardation Protein) studies in mentally retarded children in Greece | 0 | 0 |
| 2072 | 0 | 0 | 1779 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):167-167 Tayel SM; Al-Naggar RL; Ali FE; Al-Awadi SA Two-step fragile X screening program in mentally retarded males | 0 | 0 |
| 2073 | 0 | 0 | 1785 1999 FASEB JOURNAL 13(5):A703-A703 Greenough WT; Weiler IJ; Angenstein F; Klintsova A; Bauchwitz R Synthesis of the fragile X mental retardation protein at synapses: Possible role in synaptic development and plasticity | 0 | 0 |
| 2074 | 5 | 10 | 1789 1999 HEREDITAS 130(2):189-190 Sucharov CC; Silva R; Rondinelli E; Moura-Neto RS Fragile X trinucleotide repeats from a normal population in Rio de Janeiro, Brazil | 0 | 0 |
| 2075 | 0 | 0 | 1793 1999 HUMAN REPRODUCTION 14:235-235 Sermon K; Seneca S; Lissens W; De Vos A; Vandervorst M; Vanderfaellie A; Bonnefont JP; Van Steirteghem A; Liebaers I Preimplantation genetic diagnosis for fragile-X syndrome | 0 | 0 |
| 2076 | 1 | 45 | 1799 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 |
| 2077 | 0 | 0 | 1803 1999 JOURNAL OF MEDICAL GENETICS 36:S64-S64 Lazarau L; Warburton SA; Roberts CE; Hughes HE; Bartlett S; Meredith AL; Ravine D Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male | 0 | 0 |
| 2078 | 0 | 0 | 1804 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 |
| 2079 | 0 | 0 | 1807 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 |
| 2080 | 4 | 5 | 1813 1999 MEDICAL JOURNAL OF AUSTRALIA 170(12):624-624 Cohen J; Loesch DZ Fragile X syndrome: do professionals know about it? | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2081 | 0 | 0 | 1817 1999 MOLECULAR PSYCHIATRY 4:S56-S56 Fisch GS; Carpenter N; Holden JA; Pandya A; Howard-Peebles PN; Tarleton J Psychopathology in genetic disorders producing cognitive deficits: Adaptive and maladative behavior in the fragile X syndrome, Williams syndrome and neurofibromatosis type 1. | 0 | 0 |
| 2082 | 0 | 0 | 1833 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):25-25 Crawford DC; Wilson B; Sherman SL Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool-PCR. | 0 | 0 |
| 2083 | 0 | 0 | 1834 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):26-26 Hagerman RJ; Tassone F; Leehey M; Hills J; Wilson R; Landau W; Grigsby J; Gage B; Hagerman PJ Cerebellar tremor and cerebellar cortical atrophy in older males with the fragile X premutation. | 0 | 0 |
| 2084 | 0 | 0 | 1835 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P; Oostra BA Differential reactivation of the FMR1 gene in fragile X patients cell lines. | 0 | 0 |
| 2085 | 0 | 0 | 1836 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Kenneson A; Zhang F; Warren ST Fragile X premutation alleles are associated with reduced FMRP levels due to a reduction of message translatability. | 0 | 0 |
| 2086 | 0 | 0 | 1837 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):57-57 Li MM; Nelson L; Bamshad M; Ward K Fragile X mosaics in a family with multiple mildly affected individuals. | 0 | 0 |
| 2087 | 0 | 0 | 1838 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):130-130 Khalifa M; Struthers J High frequency of Klinefelter syndrome among a large population of patients referred for Fragile X syndrome testing due to undiagnosed mental retardation. | 0 | 0 |
| 2088 | 0 | 0 | 1839 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):135-135 Harris SW; Brown KE; Hills JL; Tassone F; Hagerman PJ; Taylor AK; Hagerman RJ Adaptive functioning and molecular relationships in individuals with fragile X syndrome. | 0 | 0 |
| 2089 | 0 | 0 | 1840 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):184-184 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ Clinical and molecular correlations in individuals with a fragile X full mutation. | 0 | 0 |
| 2090 | 0 | 0 | 1841 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):236-236 Mathews DJ; Hudson R; Eichier E; Chakravarti A Sequence variation and linkage disequilibrium at the fragile X syndrome locus. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2091 | 0 | 0 | 1842 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):247-247 Brown NM; Friez MJ; Longshore JW; Stenzel TT Evaluation of an automated commercially available PCR kit for determination of Fragile X (FRAXA) normal, gray-zone and premutation allele sizes. | 0 | 0 |
| 2092 | 0 | 0 | 1843 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):248-248 Murphy KM; Nunes ME Comparison of child-only versus mother/child sample collection in Fragile X testing. | 0 | 0 |
| 2093 | 0 | 0 | 1844 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):254-254 Weinhaeusel A; Skarits C; Haas OA Methylation-sensitive PCR (MS-PCR) analysis of the fragile X (FRAXA) syndrome. | 0 | 0 |
| 2094 | 0 | 0 | 1845 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):348-348 Dyack S; Steele L; Koultchitski G; Yang Y; Weksberg R; Ray PN; Pearson CE AGG interruptions in the CGG trinucleotide repeat tract of the FMR1 gene may contribute to stability of Fragile X premutations. | 0 | 0 |
| 2095 | 0 | 0 | 1847 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):365-365 O'Donnell WT; Warren ST Investigating the cause of macroorchidism in fragile X syndrome using oligonucleotide microarrays. | 0 | 0 |
| 2096 | 0 | 0 | 1848 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Parades WJ; Warren ST Meiotic stability of a fragile X premutation CGG trinucleotide repeat in a mouse model. | 0 | 0 |
| 2097 | 0 | 0 | 1849 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):415-415 Najmabadi H; Taghizadeh F; Teimourian SH; Karimi-Nejad R; Shafeghati Y; Mohammady GB; Al-Madany SN; Hoseiny SS; Karimi-Nejad MH Molecular analysis of Fragile X syndrome in Iranian population. | 0 | 0 |
| 2098 | 0 | 0 | 1850 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):428-428 Brown WT; Ding X; Idrissi AE; Scalia J; Glicksman A; Bauchwitz R; Dobkin C Fragile X transgene and embryonic lethality in mice. | 0 | 0 |
| 2099 | 3 | 11 | 1860 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):358-360 Missirian C; Moncla A; Voelckel MA; Ravix V; Philip N Fragile X syndrome and 22q11.2 microdeletion in the same sibship | 0 | 0 |
| 2100 | 5 | 19 | 1868 2000 ANNALS OF SAUDI MEDICINE 20(1):16-19 Al Husain M; Salih MAM; Zaki OK; Al Othman L; Al Nasser MN A clinical study of mentally retarded children with fragile X syndrome in Saudi Arabia | 0 | 0 |
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