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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.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1801 | 19 | 34 | 1801 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 |
| 1802 | 11 | 42 | 1802 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 | 0 | 1 |
| 1803 | 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 |
| 1804 | 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 |
| 1805 | 10 | 21 | 1805 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 |
| 1806 | 2 | 5 | 1806 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-171 Macpherson J; Murray A; Webb J; Jacobs P Fragile X syndrome: of POF and premutations | 0 | 1 |
| 1807 | 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 |
| 1808 | 12 | 18 | 1808 1999 JOURNAL OF MEDICAL GENETICS 36(3):253-257 Helderman-van den Enden ATJM; Maaswinkel-Mooij PD; Hoogendoorn E; Willemsen R; Maat-Kievit JA; Losekoot M; Oostra BA Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities | 3 | 8 |
| 1809 | 16 | 22 | 1809 1999 JOURNAL OF MEDICAL GENETICS 36(6):467-470 de Vries BBA; Mohkamsing S; van den Ouweland AMW; Mol E; Gelsema K; van Rijn M; Tibben A; Halley DJJ; Duivenvoorden HJ; Oostra BA; Niermeijer MF; Collaborative Fragile X Study Grp Screening for the fragile X syndrome among the mentally retarded: a clinical study | 2 | 8 |
| 1810 | 5 | 6 | 1810 1999 JOURNAL OF MEDICAL GENETICS 36(7):565-566 Moore SJ; Strain L; Cole GF; Miedzybrodzka Z; Kelly KF; Dean JCS Fragile X syndrome with FMR1 and FMR2 deletion | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1811 | 18 | 28 | 1811 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 |
| 1812 | 20 | 43 | 1812 1999 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 38(10):1294-1301 Murphy DGM; Mentis MJ; Pietrini P; Grady CL; Moore CJ; Horwitz B; Hinton V; Dobkin CS; Schapiro MB; Rapoport SI Premutation female carriers of fragile X syndrome: A pilot study on brain anatomy and metabolism | 6 | 7 |
| 1813 | 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 |
| 1814 | 7 | 113 | 1814 1999 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 5(4):305-313 Hagerman RJ Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome | 0 | 2 |
| 1815 | 19 | 74 | 1815 1999 MOLECULAR AND CELLULAR BIOLOGY 19(8):5675-5684 White PJ; Borts RH; Hirst MC Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism | 9 | 39 |
| 1816 | 14 | 46 | 1816 1999 MOLECULAR AND CELLULAR BIOLOGY 19(12):7925-7932 Ceman S; Brown V; Warren ST Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex | 35 | 64 |
| 1817 | 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 |
| 1818 | 6 | 30 | 1818 1999 NATURE GENETICS 22(1):98-101 Coffee B; Zhang FP; Warren ST; Reines D Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells | 25 | 92 |
| 1819 | 1 | 1 | 1819 1999 NATURE GENETICS 22(2):209-209 Coffee B Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells (vol 22, pg 98, 1999) | 2 | 5 |
| 1820 | 17 | 53 | 1820 1999 NEUROSCIENCE 94(1):185-192 Paradee W; Melikian HE; Rasmussen DL; Kenneson A; Conn PJ; Warren ST Fragile X mouse: Strain effects of knockout phenotype and evidence suggesting deficient amygdala function | 19 | 37 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1821 | 12 | 23 | 1821 1999 PRENATAL DIAGNOSIS 19(13):1223-1230 Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; Vandervorst M; Van Steirteghem A; Liebaers I Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG | 2 | 26 |
| 1822 | 14 | 43 | 1822 1999 RNA-A PUBLICATION OF THE RNA SOCIETY 5(9):1248-1258 Adinolfi S; Bagni C; Musco G; Gibson T; Mazzarella L; Pastore A Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains | 15 | 22 |
| 1823 | 10 | 20 | 1823 1999 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 27(3):175-181 Sarimski K Play and communicative behaviour in young boys with fragile-X syndrome. | 0 | 1 |
| 1824 | 22 | 40 | 1824 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(1):6-15 Tassone F; Hagerman RJ; Taylor AK; Gane LW; Godfrey TE; Hagerman PJ Elevated levels of FMR1 mRNA in carrier males: A new mechanism of involvement in the fragile-X syndrome | 49 | 82 |
| 1825 | 9 | 28 | 1825 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):413-418 Hundscheid RDL; Sistermans EA; Thomas CMG; Braat DDM; Straatman H; Kiemeney LALM; Oostra BA; Smits APT Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations | 14 | 29 |
| 1826 | 26 | 52 | 1826 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):480-493 Crawford DC; Schwartz CE; Meadows KL; Newman JL; Taft LF; Gunter C; Brown WT; Carpenter NJ; Howard-Peebles PN; Monaghan KG; Nolin SL; Reiss AL; Feldman GL; Rohlfs EM; Warren ST; Sherman SL Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population | 7 | 16 |
| 1827 | 8 | 8 | 1827 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):11-13 Sherman SL Premature ovarian failure among fragile X premutation carriers: Parent-of-origin effect? | 4 | 8 |
| 1828 | 2 | 4 | 1828 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):253-254 Murray A; Ennis S; Morton N No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers | 9 | 16 |
| 1829 | 6 | 8 | 1829 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):254-255 Vianna-Morgante AM; Costa SS Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X | 8 | 15 |
| 1830 | 3 | 3 | 1830 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):256-258 Hundscheid RDL; Thomas CMG; Braat DDM; Oostra BA; Smits APT Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X - Reply | 2 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1831 | 0 | 0 | 1831 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Jin P; Feng Y; Brown V; Warren ST Identification of polyribosomes-associated mRNAs regulated by fragile X mental retardation protein (FMRP) using oligonucleotide microarrays. | 1 | 2 |
| 1832 | 0 | 0 | 1832 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Brown V; Ceman S; Jin P; Jin C; Wilkinson KD; Warren ST Messenger RNAs associated with the fragile X mental retardation protein in mouse brain. | 1 | 1 |
| 1833 | 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 |
| 1834 | 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 |
| 1835 | 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 |
| 1836 | 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 |
| 1837 | 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 |
| 1838 | 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 |
| 1839 | 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 |
| 1840 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1841 | 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 |
| 1842 | 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 |
| 1843 | 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 |
| 1844 | 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 |
| 1845 | 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 |
| 1846 | 0 | 0 | 1846 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):360-360 Ramos FJ; Mila M; Ortilles M; Rife M; Tazon B; De Diego Y; Willemsen R Validity of the analysis of the FMRP expression in bloodsmears as a screening method for the Fragile X Syndrome. | 1 | 1 |
| 1847 | 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 |
| 1848 | 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 |
| 1849 | 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 |
| 1850 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1851 | 27 | 42 | 1851 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(4):229-236 Lachiewicz AM; Dawson DV; Spiridigliozzi GA Physical characteristics of young boys with fragile X syndrome: Reasons for difficulties in making a diagnosis in young males | 9 | 10 |
| 1852 | 8 | 22 | 1852 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(5):336-342 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Carrier testing in fragile X syndrome: Effect on self-concept | 2 | 4 |
| 1853 | 21 | 33 | 1853 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 93(2):99-106 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Macpherson JN; Brondum-Nielsen K; Hasholt L; Norgaard-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 | 2 | 6 |
| 1854 | 26 | 35 | 1854 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(3):232-236 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; Hagerman PJ Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA | 16 | 23 |
| 1855 | 3 | 24 | 1855 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(5):345-360 Fryns JP; Borghgraef M; Brown TW; Chelly J; Fisch GS; Hamel B; Hanauer A; Lacombe D; Luo L; MacPherson JN; Mandel JL; Moraine C; Mulley J; Nelson D; Oostra B; Partington M; Ramakers GJA; Ropers HH; Rousseau F; Schwartz C; Steinbach P; Stoll C; Tranebjaerg L; Turner G; Van Bokhoven H; Vianna-Morgante A; Villard L; Warren ST 9th international workshop on fragile X syndrome and X-linked mental retardation | 0 | 2 |
| 1856 | 10 | 14 | 1856 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):105-107 Tuncbilek E; Alikasifoglu M; Aktas D; Duman F; Yanik H; Anar B; Oostra B; Willemsen R Screening for the fragile X syndrome among mentally retarded males by hair root analysis | 6 | 6 |
| 1857 | 16 | 33 | 1857 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):123-129 Hjalgrim H; Hansen BF; Brondum-Nielsen K; Nolting D; Kjaer I Aspects of skeletal development in fragile X syndrome fetuses | 2 | 3 |
| 1858 | 26 | 59 | 1858 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):150-156 Backes M; Genc B; Schreck J; Doerfler W; Lehmkuhl G; von Gontard A Cognitive and behavioral profile of fragile X boys: Correlations to molecular data | 7 | 10 |
| 1859 | 12 | 46 | 1859 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):307-315 Gould EL; Loesch DZ; Martin MJ; Hagerman RJ; Armstrong SM; Huggins RM Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study | 10 | 15 |
| 1860 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1861 | 4 | 9 | 1861 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(5):516-517 Limprasert P; Jaruratanasirikul S; Vasiknanonte P Unilateral macroorchidism in fragile X syndrome | 2 | 2 |
| 1862 | 68 | 116 | 1862 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(2):153-163 Bardoni B; Mandel JL; Fisch GS FMR1 gene and fragile X syndrome | 10 | 20 |
| 1863 | 33 | 48 | 1863 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):183-188 Willemsen R; Oostra BA FMRP detection assay for the diagnosis of the fragile X syndrome | 1 | 4 |
| 1864 | 22 | 33 | 1864 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):189-194 Sherman SL Premature ovarian failure in the fragile X syndrome | 12 | 24 |
| 1865 | 27 | 40 | 1865 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):195-203 Tassone F; Hagerman RJ; Chamberlain WD; Hagerman PJ Transcription of the FMR1 gene in individuals with fragile X syndrome | 16 | 24 |
| 1866 | 14 | 37 | 1866 2000 AMERICAN JOURNAL ON MENTAL RETARDATION 105(4):286-299 Kau ASM; Reider EE; Payne L; Meyer WA; Freund L Early behavior signs of psychiatric phenotypes in fragile X syndrome | 2 | 4 |
| 1867 | 20 | 37 | 1867 2000 ANNALES DE GENETIQUE 43(1):29-34 Gonzalez-del Angel A; Vidal S; Saldana Y; del Castillo V; Alcantara MA; Macias M; Luna JP; Orozco L Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico | 2 | 3 |
| 1868 | 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 |
| 1869 | 21 | 41 | 1869 2000 ANNALS OF SAUDI MEDICINE 20(3-4):214-217 Iqbal MA; Sakati N; Nester M; Ozand P Cytogenetic diagnosis of fragile X syndrome: Study of 305 suspected cases in Saudi Arabia | 0 | 0 |
| 1870 | 5 | 8 | 1870 2000 AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE 30(1):86-88 Driscoll G; Clark J; Elakis G; Turner G Early menopause in a family carrying a fragile X premutation | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1871 | 2 | 29 | 1871 2000 BEHAVIOR RESEARCH METHODS INSTRUMENTS & COMPUTERS 32(1):5-10 Boccia ML; Roberts JE Behavior and autonomic nervous system function assessed via heart period measures: The case of hyperarousal in boys with fragile X syndrome | 8 | 9 |
| 1872 | 10 | 33 | 1872 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(3):973-980 Sung YJ; Conti J; Currie JR; Brown WT; Denman RB RNAs that interact with the Fragile X syndrome RNA binding protein FMRP | 23 | 30 |
| 1873 | 3 | 46 | 1873 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 278(3):833-838 Patel PK; Bhavesh NS; Hosur RV Cation-dependent conformational switches in d-TGGCGGC containing two triplet repeats of Fragile X Syndrome: NMR observations | 4 | 9 |
| 1874 | 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 |
| 1875 | 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 |
| 1876 | 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 |
| 1877 | 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 |
| 1878 | 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 |
| 1879 | 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 |
| 1880 | 6 | 13 | 1880 2000 CLINICAL GENETICS 57(6):456-458 Lisik M The comparison of anthropometric variables in mentally retarded boys with and without fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1881 | 20 | 33 | 1881 2000 CLINICAL GENETICS 58(2):111-115 Kallinen J; Heinonen S; Mannermaa A; Ryynanen M Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation | 3 | 5 |
| 1882 | 23 | 46 | 1882 2000 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 42(11):768-774 Sheldon L; Turk J Monozygotic boys with fragile X syndrome | 1 | 2 |
| 1883 | 18 | 32 | 1883 2000 EPILEPSIA 41(1):19-23 Musumeci SA; Bosco P; Calabrese G; Bakker C; De Sarro GB; Elia M; Ferri R; Oostra BA Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome | 23 | 30 |
| 1884 | 9 | 21 | 1884 2000 EUROPEAN JOURNAL OF HUMAN GENETICS 8(4):247-252 Murray A; Ennis S; MacSwiney F; Webb J; Morton NE Reproductive and menstrual history of females with fragile X expansions | 10 | 13 |
| 1885 | 0 | 0 | 1885 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:305-305 Beckel-Mitchener AC; Weiler IJ; Klintsova AY; Harms L; Belt B; Spangler CC; Greenough WT Analysis of protein synthesis in Fragile X knockout mice | 0 | 0 |
| 1886 | 0 | 18 | 1886 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12(1):381-384 Miller WJ; Skinner JA; Foss GS; Davies KE Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain | 0 | 7 |
| 1887 | 0 | 0 | 1887 2000 GENETIC COUNSELING 11(3):281-311 [Anon] ACTS: Of the 9th International Workshop on Fragile X Syndrome and X Linked Mental Retardation August 23-25, 1999, Le Bischenberg, Strasbourg, France - Abstracts | 0 | 0 |
| 1888 | 9 | 16 | 1888 2000 GENETIC TESTING 4(3):235-239 Tzountzouris J; Kennedy D; Skuterud M; Connolly-Wilson M; Holden JJA; Lin CC; Mak-Tam E; Somerville MJ; Summers AM; Allingham-Hawkins DJ Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome | 0 | 1 |
| 1889 | 5 | 10 | 1889 2000 GENETIC TESTING 4(3):241-242 Brown WT; Nolin SL Apparent FMR1 allele instability in non-Fragile X males - Invited commentary | 0 | 1 |
| 1890 | 16 | 20 | 1890 2000 GENETIC TESTING 4(3):289-292 Geva E; Yaron Y; Shomrat R; Ben-Yehuda A; Zabari S; Peretz H; Naiman T; Yeger H; Orr-Urtreger A The risk of Fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known Fragile X families | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1891 | 27 | 44 | 1891 2000 GENETICS IN MEDICINE 2(4):242-248 Burman RW; Anoe KS; Popovich BW Fragile X full mutations ave more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics | 1 | 2 |
| 1892 | 11 | 12 | 1892 2000 HUMAN GENETICS 106(3):366-369 Arocena DG; de Diego Y; Oostra BA; Willemsen R; Rodriguez MM A fragile X case with an amplification/deletion mosaic pattern | 0 | 0 |
| 1893 | 3 | 6 | 1893 2000 HUMAN GENETICS 107(2):195-196 Castellvi-Bel S; Fernandez-Burriel M; Rife M; Jimenez D; Mallolas J; Sanchez A; Ramos F; Mila M Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles | 1 | 2 |
| 1894 | 46 | 82 | 1894 2000 HUMAN MOLECULAR GENETICS 9(6):901-908 Jin P; Warren ST Understanding the molecular basis of fragile X syndrome | 36 | 73 |
| 1895 | 23 | 55 | 1895 2000 HUMAN MOLECULAR GENETICS 9(10):1487-1493 Tamanini F; Kirkpatrick LL; Schonkeren J; van Unen L; Bontekoe C; Bakker C; Nelson DL; Galjaard H; Oostra BA; Hoogeveen AT The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins | 7 | 12 |
| 1896 | 31 | 62 | 1896 2000 HUMAN MOLECULAR GENETICS 9(12):1759-1769 Crawford DC; Zhang FP; Wilson B; Warren ST; Sherman SL Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability | 5 | 10 |
| 1897 | 25 | 55 | 1897 2000 HUMAN MOLECULAR GENETICS 9(19):2909-2918 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 | 3 | 9 |
| 1898 | 0 | 0 | 1898 2000 HUMAN REPRODUCTION 15:12-12 Apessos A; Harper J; Delhanty JDA Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers | 0 | 0 |
| 1899 | 0 | 0 | 1899 2000 HUMAN REPRODUCTION 15:47-48 Hundscheid RDL; Sistermans EA; Thomas CMG; Straatman H; Kiemeney LALM; Oostra BA; Smits APT; Braat DDM Shorter reproductive life and a high risk for premature ovarian failure (POF) in women who have inherited fragile X premutations from their fathers | 0 | 0 |
| 1900 | 16 | 41 | 1900 2000 HUMAN REPRODUCTION 15(1):197-202 Marozzi A; Vegetti W; Manfredini E; Tibiletti MG; Testa G; Crosignani PG; Ginelli E; Meneveri R; Dalpra L Association between idiopathic premature ovarian failure and fragile X premutation | 10 | 29 |
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Version: 2004.08.24