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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 |
|---|---|---|---|---|---|
| 1701 | 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 |
| 1702 | 15 | 24 | 1702 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(1):98-103 Willemsen R; Anar B; Otero YD; de Vries BBA; Hilhorst-Hofstee Y; Smits A; van Looveren E; Willems PJ; Galjaard H; Oostra BA Noninvasive test for fragile X syndrome, using hair root analysis | 18 | 20 |
| 1703 | 22 | 52 | 1703 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(3):680-688 Nolin SL; Houck GE; Gargano AD; Blumstein H; Dobkin CS; Brown WT FMR1 CCG-repeat instability by single sperm and lymphocytes of fragile-X premutation males | 7 | 15 |
| 1704 | 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 |
| 1705 | 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 |
| 1706 | 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 |
| 1707 | 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 |
| 1708 | 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 |
| 1709 | 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 |
| 1710 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1711 | 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 |
| 1712 | 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 |
| 1713 | 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 |
| 1714 | 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 |
| 1715 | 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 |
| 1716 | 0 | 0 | 1716 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A403-A403 Xu B; School JM; Buroker NE; Scott CR; Chen SH High frequency of the FMR-1 INV10+14c/t polymorphism in Asians, and its association with the Fragile X Syndrome in Caucasians. | 0 | 1 |
| 1717 | 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 |
| 1718 | 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 |
| 1719 | 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 |
| 1720 | 27 | 53 | 1720 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(1):25-30 Abrams MT; Kaufmann WE; Rousseau F; Oostra BA; Wolozin B; Taylor CV; Lishaa N; Morel ML; Hoogeveen A; Reiss AL FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome | 8 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1721 | 5 | 20 | 1721 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(3):206-211 McConkie-Rosell A; Spiridigliozzi GA; Rounds K; Dawson DV; Sullivan JA; Burgess D; Lachiewicz AM Parental attitudes regarding carrier testing in children at risk for fragile X syndrome | 2 | 7 |
| 1722 | 0 | 5 | 1722 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(2):140-141 Hjalgrim H; Jacobsen TB; Norgaard K; Lou HC; Brondum-Nielsen K; Jonassen O Frontal-subcortical hypofunction in the fragile X syndrome | 5 | 6 |
| 1723 | 36 | 61 | 1723 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):221-236 Holden JJA; Percy M; Allingham-Hawkins D; Brown WT; Chiurazzi P; Fisch G; Gane L; Gunter C; Hagerman R; Jenkins EC; Kooy RF; Lubs HA; Murray A; Neri G; Schwartz C; Tranebjaerg L; Villard L; Willems PJ Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997 | 1 | 4 |
| 1724 | 6 | 35 | 1724 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):248-252 Weiler IJ; Greenough WT Synaptic synthesis of the Fragile X protein: Possible involvement in synapse maturation and elimination | 27 | 42 |
| 1725 | 8 | 23 | 1725 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):253-256 Fisch GS; Holden JJK; Carpenter NJ; Howard-Peebles PN; Maddalena A; Pandya A; Nance W Age-related language characteristics of children and adolescents with fragile X syndrome | 7 | 8 |
| 1726 | 13 | 26 | 1726 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):257-263 Fisch GS; Carpenter NJ; Holden JJA; Simensen R; Howard-Peebles PN; Maddalena A; Pandya A; Nance W Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: Growth, development, and profiles | 7 | 7 |
| 1727 | 16 | 54 | 1727 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):268-279 Miller LJ; McIntosh DN; 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 syndrome: A preliminary report | 29 | 36 |
| 1728 | 4 | 9 | 1728 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):281-285 Teisl JT; Reiss AL; Mazzocco MMM Maximizing the sensitivity of a screening questionnaire for determining fragile X at-risk status | 2 | 2 |
| 1729 | 27 | 47 | 1729 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):286-295 Kaufmann WE; Abrams MT; Chen WM; Reiss AL Genotype, molecular phenotype, and cognitive phenotype: Correlations in fragile X syndrome | 27 | 33 |
| 1730 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1731 | 4 | 28 | 1731 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):298-301 Kotilainen J; Pirinen S Dental maturity is advanced in fragile X syndrome | 2 | 2 |
| 1732 | 19 | 35 | 1732 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):302-307 Parvari R; Mumm S; Galil A; Manor E; Bar-David Y; Carmi R Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth | 2 | 6 |
| 1733 | 11 | 20 | 1733 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):308-312 Fisch GS; Carpenter N; Holden JJA; Howard-Peebles PN; Maddalena A; Borghgraef M; Steyaert J; Fryns JP Longitudinal changes in cognitive and adaptive behavior in fragile X females: A prospective multicenter analysis | 9 | 14 |
| 1734 | 13 | 41 | 1734 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):313-317 Hagerman RJ; Hills J; Scharfenaker S; Lewis H Fragile X syndrome and selective mutism | 11 | 18 |
| 1735 | 10 | 22 | 1735 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):318-321 Linden MG; Tassone F; Gane LW; Hills JL; Hagerman RJ; Taylor AK Compound heterozygous female with fragile X syndrome | 0 | 1 |
| 1736 | 3 | 6 | 1736 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):322-325 Allingham-Hawkins SJ; Babul-Hirji R; Chitayat D; Holden JJA; Yang KT; Lee C; Hudson R; Gorwill H; Nolin SL; Glicksman A; Jenkins EC; Brown WT; Howard-Peebles PN; Becchi C; Cummings E; Fallon L; Seitz S; Black SH; Vianna-Morgante AM; Costa SS; Otto PA; Mingroni-Netto RC; Murray A; Webb J; MacSwinney F; Dennis N; Jacobs PA; Syrrou M; Georgiou I; Patsalis PC; Uzielli MLG; Guarducci S; Lapi E; Cecconi A; Ricci U Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data | 10 | 19 |
| 1737 | 4 | 6 | 1737 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):326-326 Vianna-Morgante AM Twinning and premature ovarian failure in premutation fragile X carriers | 8 | 9 |
| 1738 | 5 | 11 | 1738 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):327-328 Braat DDM; Smits APT; Thomas CMG Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: A pilot study | 8 | 11 |
| 1739 | 3 | 9 | 1739 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):331-333 Wen GY; Jenkins EC; Goldberg EM; Genovese M; Brown WT; Wisniewski HM Ultrastructure of the fragile X chromosome: New observations on the fragile site | 0 | 3 |
| 1740 | 6 | 11 | 1740 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):338-341 Dobkin C; Ding XH; Li SY; Houck G; Nolin SL; Glicksman A; Zhong N; Jenkins EC; Brown WT Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1741 | 7 | 14 | 1741 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):342-346 Jenkins EC; Wen GY; Kim KS; Zhong N; Sapienza VJ; Hong H; Chen J; Li SY; Houck GE; Ding XH; Nolin SL; Dobkin CS; Brown WT Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies | 2 | 2 |
| 1742 | 10 | 14 | 1742 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):347-349 Chiurazzi P; Pomponi MG; Sharrock A; Macpherson J; Lormeau S; Morel ML; Rousseau F DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature | 2 | 10 |
| 1743 | 3 | 7 | 1743 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):350-351 Faradz SMH; Buckley M; Tang LP; Leigh D; Holden JJA Molecular screening for fragile X syndrome among Indonesian children with developmental disability | 3 | 4 |
| 1744 | 18 | 37 | 1744 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):184-190 Patsalis PC; Sismani C; Hettinger JA; Boumba I; Georgiou I; Stylianidou G; Anastasiadou V; Koukoulli R; Pagoulatos G; Syrrou M Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: Incidence, genetic variation, and stability | 7 | 18 |
| 1745 | 20 | 34 | 1745 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):191-194 Zhong N; Ju WN; Xu WM; Ye LL; Shen Y; Wu GY; Chen SH; Jin RM; Hu XF; Yang AD; Liu XX; Poon P; Pang C; Zheng Y; Song L; Zhao P; Fu BJ; Gu HJ; Brown WT Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians | 6 | 10 |
| 1746 | 4 | 5 | 1746 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):202-203 Tuncbilek E; Alikasifoglu M; Boduroglu K; Aktas D; Anar B Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology | 3 | 3 |
| 1747 | 20 | 26 | 1747 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):204-207 Mingroni-Netto RC; Costa SS; Angeli CB; Vianna-Morgante AM DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population | 0 | 3 |
| 1748 | 10 | 14 | 1748 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):214-216 Pekarik V; Blazkova M; Kozak L Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic | 1 | 3 |
| 1749 | 19 | 25 | 1749 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):221-225 Schmucker B; Seidel J Mosaicism for a full mutation and a normal size allele in two fragile X males | 4 | 6 |
| 1750 | 10 | 20 | 1750 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):226-228 Glaser D; Wohrle D; Salat U; Vogel W; Steinbach P; Mucke J Mitotic behavior of expanded CGG repeats studied on cultured cells: Further evidence for methylation-mediated triplet repeat stability in fragile X syndrome | 4 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1751 | 17 | 22 | 1751 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):229-232 Petek E; Kroisel PM; Schuster M; Zierler H; Wagner K Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene | 1 | 1 |
| 1752 | 31 | 40 | 1752 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):233-239 Taylor AK; Tassone F; Dyer PN; Hersch SM; Harris JB; Greenough WT; Hagerman RJ Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome | 15 | 23 |
| 1753 | 20 | 37 | 1753 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):245-249 Reyniers E; Martin JJ; Cras P; Van Marck E; Handig I; Jorens HZJ; Oostra BA; Kooy RF; Willems PJ Postmortem examination of two fragile X brothers with an FMR1 full mutation | 14 | 19 |
| 1754 | 44 | 64 | 1754 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):250-261 Tassone F; Hagerman RJ; Ikle DN; Dyer PN; Lampe M; Willemsen R; Oostra BA; Taylor AK FMRP expression as a potential prognostic indicator in fragile X syndrome | 52 | 62 |
| 1755 | 14 | 23 | 1755 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):268-271 Zhong N; Ju W; Nelson D; Dobkin C; Brown WT Reduced mRNA for G3BP in fragile X cells: Evidence of FMR1 gene regulation | 3 | 5 |
| 1756 | 4 | 36 | 1756 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):272-276 Currie JR; Brown WT KH domain-containing proteins of yeast: Absence of a fragile X gene homologue | 0 | 4 |
| 1757 | 11 | 27 | 1757 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):300-303 Uzielli MLG; Guarducci S; Lapi E; Cecconi A; Ricci U; Ricotti G; Biondi C; Scarselli B; Vieri F; Scarnato P; Gori F; Sereni A Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data | 11 | 24 |
| 1758 | 4 | 11 | 1758 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):306-308 Syrrou M; Georgiou I; Patsalis PC; Bouba I; Adonakis G; Papoulatos GN Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction | 1 | 9 |
| 1759 | 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 |
| 1760 | 5 | 13 | 1760 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):197-201 Freedenberg DL; Gane LW; Richards CS; Lampe M; Hills J; O'Connor R; Manchester D; Taylor A; Tassone F; Hulseberg D; Hagerman RJ; Patil SR Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1761 | 10 | 14 | 1761 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):311-316 Grasso M; Faravelli F; Lo Nigro C; Chiurazzi P; Sperandeo MP; Argusti A; Pomponi MG; Lecora M; Sebastio GF; Perroni L; Andria G; Neri G; Bricarelli FD Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients | 1 | 1 |
| 1762 | 7 | 12 | 1762 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 86(2):162-164 Sun YJ; Baumer A Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts | 1 | 3 |
| 1763 | 5 | 12 | 1763 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(4):366-368 Torrioli MG; Vernacotola S; Mariotti P; Bianchi E; Calvani M; De Gaetano A; Chiurazzi P; Neri G Double-blind, placebo-controlled study of L-acetylcarnitine for the treatment of hyperactive behavior in fragile X syndrome | 3 | 5 |
| 1764 | 3 | 6 | 1764 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(5):436-439 Einfeld S; Tonge B; Turner G Longitudinal course of behavioral and emotional problems in Fragile X syndrome | 5 | 5 |
| 1765 | 88 | 136 | 1765 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 88(1):11-24 Kaufmann WE; Reiss AL Molecular and cellular genetics of fragile X syndrome | 15 | 26 |
| 1766 | 17 | 24 | 1766 1999 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 181(4):789-792 Wenstrom KD; Descartes M; Franklin J; Cliver SP A five-year experience with fragile X screening of high-risk gravid women | 1 | 1 |
| 1767 | 21 | 38 | 1767 1999 ANNALES DE GENETIQUE 42(4):197-201 Arrieta I; Criado B; Martinez B; Telez M; Nunez T; Penagarikano O; Ortega B; Lostao CM A survey of fragile X syndrome in a sample from Spanish Basque country | 3 | 4 |
| 1768 | 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 |
| 1769 | 0 | 0 | 1769 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-768 Lanham DC; Mazzocco MM; Denckla MB Depression and anxiety in girls with Fragile X or Turner Syndrome. | 1 | 1 |
| 1770 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1771 | 17 | 36 | 1771 1999 BIOCHEMICAL JOURNAL 343:517-523 Tamanini F; van Unen L; Bakker C; Sacchi N; Galjaard H; Oostra BA; Hoogeveen AT Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P | 15 | 20 |
| 1772 | 46 | 98 | 1772 1999 BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE 77(4):331-342 Khandjian EW Biology of the fragile X mental retardation protein, an RNA-binding protein | 12 | 22 |
| 1773 | 34 | 44 | 1773 1999 CLINICAL GENETICS 55(5):346-351 Tassone F; Longshore J; Zunich J; Steinbach P; Salat U; Taylor AK Tissue-specific methylation differences in a fragile X premutation carrier | 2 | 4 |
| 1774 | 8 | 12 | 1774 1999 CLINICAL GENETICS 56(1):98-99 Millan JM; Martinez F; Cadroy A; Gandia J; Casquero M; Beneyto M; Badin L; Prieto F Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain | 2 | 3 |
| 1775 | 15 | 30 | 1775 1999 CORTEX 35(2):263-271 Cornish KM; Munir F; Cross G Spatial cognition in males with Fragile-X syndrome: Evidence for a neuropsychological phenotype | 12 | 14 |
| 1776 | 35 | 50 | 1776 1999 CURRENT OPINION IN PSYCHIATRY 12(5):573-578 Harris SW; Hagerman RJ Fragile X syndrome: new developments | 2 | 2 |
| 1777 | 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 |
| 1778 | 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 |
| 1779 | 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 |
| 1780 | 13 | 65 | 1780 1999 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 41(9):625-632 Hatton DD; Bailey DB; Hargett-Beck MQ; Skinner M; Clark RD Behavioral style of young boys with fragile X syndrome | 8 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1781 | 16 | 23 | 1781 1999 DIAGNOSTIC MOLECULAR PATHOLOGY 8(3):152-156 Tzeng CC; Cho WC; Kuo PL; Chen RM Pilot fragile X screening in normal population of Taiwan | 7 | 9 |
| 1782 | 22 | 54 | 1782 1999 EPILEPSIA 40(8):1092-1099 Musumeci SA; Hagerman RJ; Ferri R; Bosco P; Dalla Bernardina B; Tassinari CA; De Sarro GB; Elia M Epilepsy and EEG findings in males with fragile X syndrome | 9 | 18 |
| 1783 | 14 | 23 | 1783 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(2):212-216 Ryynanen M; Heinonen S; Makkonen M; Kajanoja E; Mannermaa A; Pertti K Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies | 12 | 16 |
| 1784 | 18 | 33 | 1784 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(5):526-532 Kooy RF; Reyniers E; Verhoye M; Sijbers J; Bakker CE; Oostra BA; Willems PJ; Van der Linden A Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging | 7 | 20 |
| 1785 | 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 |
| 1786 | 13 | 21 | 1786 1999 GENETIC TESTING 3(3):301-304 Melis MA; Addis M; Lepiani C; Congeddu E; Cossu P; Cao A A strategy for fragile-X carrier screening | 0 | 2 |
| 1787 | 3 | 8 | 1787 1999 GENETICS AND MOLECULAR BIOLOGY 22(2):169-172 Pena SDJ; Sturzeneker R Diagnosis of the fragile X syndrome in males using methylation-specific PCR of the FMR1 locus | 0 | 2 |
| 1788 | 5 | 14 | 1788 1999 GENETICS AND MOLECULAR BIOLOGY 22(4):471-474 Vianna-Morgante AM; Costa SS; Pavanello RDM; Otto PA; Mingroni-Netto RC Premature ovarian failure (POF) in Brazilian fragile X carriers | 1 | 4 |
| 1789 | 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 |
| 1790 | 17 | 50 | 1790 1999 HUMAN MOLECULAR GENETICS 8(5):863-869 Tamanini F; Bontekoe C; Bakker CE; van Unen L; Anar B; Willemsen R; Yoshida M; Galjaard H; Oostra BA; Hoogeveen AT Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations | 26 | 36 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1791 | 17 | 39 | 1791 1999 HUMAN MOLECULAR GENETICS 8(13):2557-2566 Bardoni B; Schenck A; Mandel JL A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein | 26 | 44 |
| 1792 | 16 | 32 | 1792 1999 HUMAN MUTATION 14(1):71-79 Panagopoulos I; Lassen C; Kristoffersson U; Aman P A methylation PCR approach for detection of fragile X syndrome | 3 | 4 |
| 1793 | 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 |
| 1794 | 0 | 0 | 1794 1999 HUMAN REPRODUCTION 14:354-355 Gersak K; Kregar-Velikonja N; Meden-Vrtovec H; Peterlin B Fragile X premutation screening in women with premature menopause | 1 | 1 |
| 1795 | 9 | 29 | 1795 1999 INTERNATIONAL JOURNAL OF BEHAVIORAL DEVELOPMENT 23(2):519-531 Burack JA; Shulman C; Katzir E; Schaap T; Brennan JM; Iarocci G; Wilansky P; Amir N Cognitive and behavioural development of Israeli males with fragile X and Down Syndrome | 1 | 1 |
| 1796 | 59 | 96 | 1796 1999 INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 3(6):639-645 Pimentel MMG Fragile X syndrome | 0 | 5 |
| 1797 | 7 | 41 | 1797 1999 JOURNAL OF BIOLOGICAL CHEMISTRY 274(18):12797-12802 Fry M; Loeb LA Human Werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)(n) | 9 | 96 |
| 1798 | 7 | 18 | 1798 1999 JOURNAL OF CHILD NEUROLOGY 14(2):108-112 Singh R; Sutherland GR; Manson J Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndrome | 1 | 1 |
| 1799 | 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 |
| 1800 | 8 | 10 | 1800 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:47-53 Carmichael B; Pembrey M; Turner G; Barnicoat A Diagnosis of fragile-X syndrome: the experiences of parents | 9 | 11 |
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