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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
Page 3: 1 (A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT) 2 (AMERICAN JOURNAL OF HUMAN GENETICS) 3 (AMERICAN JOURNAL OF HUMAN GENETICS) 4 (AMERICAN JOURNAL OF HUMAN GENETICS) 5 (AMERICAN JOURNAL OF MEDICAL GENETICS) 6 (AMERICAN JOURNAL OF MEDICAL GENETICS) 7 (AMERICAN JOURNAL OF MEDICAL GENETICS) 8 (AMERICAN JOURNAL OF MEDICAL GENETICS) 9 (AMERICAN JOURNAL OF MEDICAL GENETICS) 10 (ANNALS OF NEUROLOGY) 11 (BIOPHYSICAL JOURNAL) 12 (CLINICAL GENETICS) 13 (CURRENT BIOLOGY) 14 (DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY) 15 (GENETIC TESTING) 16 (HUMAN GENETICS) 17 (JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION) 18 (JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS) 19 (JOURNAL OF MEDICAL GENETICS) 20 (JOURNAL OF NEUROSCIENCE RESEARCH) 21 (MEDICAL ANTHROPOLOGY QUARTERLY) 22 (NATURE REVIEWS NEUROSCIENCE) 23 (PEDIATRIC RESEARCH) 24 (REVISTA DE NEUROLOGIA)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 201 | 0 | 0 | 1275 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):965-965 NOLIN SL; GLICKSMAN A; LEWIS FA; YE LL; HOUCK GE; ASHLEY AE; SHERMAN SL; BROWN WT EVIDENCE FOR A FAMILIAL FACTOR INVOLVED IN CGG REPEAT EXPANSION IN FRAGILE-X SYNDROME | 0 | 0 |
| 202 | 0 | 0 | 1276 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1088-1088 CURLEY D; ZHONG N; WANG DW; JU W; DOBKIN C; BROWN WT NEW INTRAGENIC ALU POLYMORPHISMS IN THE FRAGILE-X GENE | 0 | 0 |
| 203 | 0 | 0 | 1277 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1218-1218 FALIKBORENSTEIN TC; YALON M; SHACHAK L; DAR C; BOROCHOWITZ Z; NELSON DL; MACPHERSON JN; EICHLER EE LONG UNINTERRUPTED CGG REPEATS WITHIN THE FMR1 GENE - POSSIBLE MECHANISM FOR THE PREVALENCE OF THE FRAGILE-X SYNDROME AMONG TUNISIAN JEWS | 0 | 0 |
| 204 | 0 | 0 | 1278 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1273-1273 MILA M; CASTELLVIBEL S; BARCELO A; SANCHEZ A; JIMENEZ D; MANDEL JL; ESTIVILL X MUTATIONS IN THE CPG ISLAND OF THE FMR1 GENE - ARE THEY RESPONSIBLE FOR FRAGILE-X SYNDROME | 0 | 0 |
| 205 | 0 | 0 | 1279 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1300-1300 PULKKINEN L; MANNERMAA A; KAJANOJA E; RYYNANANEN M; SAARIKOSKI S DELETION IN THE FMR1 GENE IN A FRAGILE-X-MALE | 0 | 0 |
| 206 | 0 | 0 | 1280 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1344-1344 WILLEMSEN R; BAKKER C; MANDEL JL; DEVRIES B; DEVYS D; OOSTRA BA RAPID SCREENING-TEST FOR FRAGILE-X SYNDROME | 0 | 0 |
| 207 | 0 | 0 | 1281 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1395-1395 HART PS; OLSON SM; CRANDALL K; TARLETON J FRAGILE-X SYNDROME RESULTING FROM A 400 BASEPAIR DELETION WITHIN THE FMR1 GENE | 0 | 2 |
| 208 | 0 | 0 | 1282 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1407-1407 JOHNSON JP; CURRY C; MICEK M; LOUIE E; ABRAMS L; DIETZ L TRANSMISSION OF STABLE AND UNSTABLE PREMUTATIONS FROM GREAT-GRANDMOTHER AND GREAT-GRANDFATHER RESPECTIVELY - LESSONS FOR GENETIC-COUNSELING IN FRAGILE-X SYNDROME FAMILIES | 0 | 0 |
| 209 | 0 | 0 | 1283 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1603-1603 BUCHANAN JA; KLOCK RJ; DORAN K; KENNEDY D; WYATT P PRENATAL TEST FOR FRAGILE-X SYNDROME REVEALS APPARENT FMR1 GENE CONTRACTION | 0 | 0 |
| 210 | 0 | 0 | 1284 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1676-1676 SHAPIRO LR; WILMOT PL; MARINELLO MJ NONINDUCED FRAGILE-X CHROMOSOMES DETECTED IN ROUTINE AMNIOTIC-FLUID CELL-CULTURE - DETERMINATION OF SIGNIFICANCE | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 211 | 0 | 0 | 1285 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1705-1705 DEVRIES BBA; VANDENOUWELAND AMW; MOHKAMSING S; HALLEY DJJ; TIBBEN A; OOSTRA BA; GALJAARD H; NIERMEIJER MF ACCEPTANCE OF SCREENING FOR THE FRAGILE-X SYNDROME AMONG 1878 MENTALLY-RETARDED INDIVIDUALS IN INSTITUTES AND SPECIAL SCHOOLS IN THE NETHERLANDS | 0 | 0 |
| 212 | 0 | 0 | 1286 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1838-1838 EIGEL A; ZYGULSKA M; DOLSCHEID T; BOGDANOVA N; DWORNICZAK B; STEGER F; SANGUANSERMSRI T; FLATZ G; HORST J FRAGILE-X PREMUTATION FREQUENCY IN NORTHERN THAILAND | 0 | 0 |
| 213 | 1 | 1 | 1287 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1914-1914 GOONEWARDENA P; ZHANG J A SINGLE TUBE NONRADIOACTIVE PCR ASSAY FOR THE DETECTION OF THE FULL SPECTRUM OR FMR1 CGG REPEATS SEEN IN THE NORMAL, CARRIER AND FRAGILE-X SYNDROME INDIVIDUALS | 0 | 0 |
| 214 | 0 | 0 | 1288 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1921-1921 JOHNSON DB; QUAN F; BUCHANNAN JA; POPOVICH BW ALLELIC SIZE LADDERS FCR THE ACCURATE SIZING OF TRINUCLEOTIDE REPEATS IN HUNTINGTON DISEASE AND FRAGILE-X SYNDROME | 0 | 0 |
| 215 | 0 | 0 | 1289 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1941-1941 TSAI MS; CHIEN TY; YANG YL; CHEN HR; HWANG SM IDENTIFICATION OF THE NUMBER OF THE FRAGILE-X SYNDROME CGG REPEAT USING SILVER STAIN | 0 | 0 |
| 216 | 11 | 21 | 1290 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(5):991-993 SHERMAN SL THE HIGH PREVALENCE OF FRAGILE-X PREMUTATION CARRIER FEMALES - IS THIS FREQUENCY UNIQUE TO THE FRENCH-CANADIAN POPULATION | 7 | 14 |
| 217 | 33 | 42 | 1291 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(5):1006-1018 ROUSSEAU F; ROUILLARD P; MOREL ML; KHANDJIAN EW; MORGAN K PREVALENCE OF CARRIERS OF PREMUTATION-SIZE ALLELES OF THE FMRI GENE AND IMPLICATIONS FOR THE POPULATION-GENETICS OF THE FRAGILE-X SYNDROME | 78 | 105 |
| 218 | 20 | 27 | 1292 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1408-1413 LOESCH DZ; HUGGINS R; PETROVIC V; SLATER H EXPANSION OF THE CGG REPEAT IN FRAGILE-X IN THE FMR1 GENE DEPENDS ON THE SEX OF THE OFFSPRING | 5 | 12 |
| 219 | 26 | 42 | 1293 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1414-1425 ASHLEY AE; SHERMAN SL POPULATION-DYNAMICS OF A MEIOTIC MITOTIC EXPANSION MODEL FOR THE FRAGILE-X SYNDROME | 13 | 20 |
| 220 | 14 | 20 | 1394 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(1):237-239 Antinolo G; Borrego S; Cabeza JC; Sanchez R; Sanchez J; Sanchez B Reverse mutation in fragile X syndrome | 7 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 221 | 6 | 13 | 1395 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(3):641-643 Brown WT; Zhong N; Dobkin C Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution | 6 | 12 |
| 222 | 4 | 21 | 1396 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(5):906-913 Knight SJL; Ritchie RJ; Chakrabarti L; Cross G; Taylor GR; Mueller RF; Hurst J; Paterson J; Yates JRW; Dow DJ; Davies KE A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom | 11 | 41 |
| 223 | 15 | 37 | 1397 1996 AMERICAN JOURNAL OF HUMAN GENETICS 59(3):540-546 Vaisanen ML; Haataja R; Leisti L Decrease in the CGG(n) trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission | 4 | 9 |
| 224 | 24 | 41 | 1526 1997 AMERICAN JOURNAL OF HUMAN GENETICS 60(1):103-112 FalikZaccai TC; Shachak E; Yalon M; Lis Z; Borochowitz Z; Macpherson JN; Nelson DL; Eichler EE Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype | 15 | 26 |
| 225 | 22 | 35 | 1527 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(3):660-667 deVries BBA; vandenOuweland AMW; Mohkamsing S; Duivenvoorden HJ; Mol E; Gelsema K; vanRijn M; Halley DJJ; Sandkuijl LA; Oostra BA; Tibben A; Niermeijer MF Screening and diagnosis for the fragile X syndrome among the mentally retarded: An epidemiological and psychological survey | 35 | 70 |
| 226 | 0 | 0 | 1528 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Fisch GS; Holden JJA; Chalifoux M; Carpenter NJ; Howard-Peebles PN; Maddalena A; Simensen R; Tarleton J; Borghgraef M; Steyaert J; Fryns JP Natural history of cognitive and adaptive behavior in young fragile X males and females: A 6-year prospective multicenter study. | 0 | 0 |
| 227 | 0 | 0 | 1529 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Kenneson A; Cramer DW; Warren ST The fragile X premutation is not a major risk for early menopause. | 0 | 0 |
| 228 | 0 | 0 | 1530 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A26-A26 Corbin F; Bouillon M; Rousseau F; Khandjian EW The fragile-X mental retardation protein is a mRNA chaperone associated with translating complexes. | 0 | 0 |
| 229 | 0 | 0 | 1531 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A26-A26 Brown VL; Small K; Lakkis L; Wilkinson KD; Warren ST Purification and characterization of the fragile X mental retardation protein. | 0 | 0 |
| 230 | 0 | 0 | 1532 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A33-A33 Ju W; Xu WM; Hwang YW; Brown WT; Zhong N Molecular pathogenetic studies of the fragile X syndrome: Double knockouts of FMR1 and FXR1 affect early development of Xenopus oocytes. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 231 | 0 | 0 | 1533 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A100-A100 Hagerman RJ; Staley-Gane L; Linden MG; Tassone F; Hills J; Taylor AK A compound heterozygous female with fragile X syndrome. | 0 | 0 |
| 232 | 0 | 0 | 1534 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A109-A109 Perroni L; Grasso M; Garavelli L; Argusti A; Cavani S; Lo Nigro C; Bricarelli FD Three cases of high functioning fragile X males | 0 | 0 |
| 233 | 0 | 0 | 1535 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A110-A110 Rhee LE; Hatcher SL; Robb KM; Towner DR Fragile X syndrome associated with birth defects. | 0 | 0 |
| 234 | 0 | 0 | 1536 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A128-A128 Jenkins EC; Wen GY; Goldberg EM; Genovese M; Brown WT; Wisniewski HM Fragile X chromosome longitudinal sections studied by transmission electron microscopy. | 0 | 0 |
| 235 | 0 | 0 | 1537 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Osthus RC; DiMaio MS; Mahoney MJ; Bale AE Significance of borderline fragile X premutations. | 0 | 0 |
| 236 | 0 | 0 | 1538 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Paradee W; Rasmussen D; Melikian H; Conn PJ; Warren ST Hippocampus-independent deficits in the Fragile X mouse. | 0 | 0 |
| 237 | 0 | 0 | 1539 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A170-A170 Feng Y; Absher D; Brown V; Eberhart DE; Malter HE; Warren ST FMRP associates with polyribosomes as an mRNP and the I304N mutation causing severe fragile X syndrome abolishes this association. | 0 | 0 |
| 238 | 0 | 0 | 1540 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A175-A175 Kaufmann WE; Abrams MT; Chen W; Reiss AL Genotype and molecular phenotype in fragile X syndrome. | 0 | 0 |
| 239 | 0 | 0 | 1541 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A192-A192 Staley-Gane L; Holloway SL; Flynn L; Logan L; Hageman RJ Assessment of patient agenda prior to genetic counseling for fragile X syndrome. | 0 | 0 |
| 240 | 0 | 0 | 1542 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A219-A219 de Vries BBA; van den Ouweland AMW; Mohkamsing S; Duivenvoorden HJ; Halley DJJ; Sandkuijl LA; Oostra BA; Tibben A; Niermeijer MF A fragile X screening program in The Netherlands: prevalence of fragile X syndrome lower than previously considered, but the disorder is still underdiagnosed. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 241 | 0 | 0 | 1543 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A304-A304 Bat O; Kimmel M; Axelrod DE; Chakraborty R Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease. | 0 | 0 |
| 242 | 0 | 0 | 1544 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A306-A306 Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G In vitro reactivation of the fragile X syndrome gene. | 1 | 1 |
| 243 | 0 | 0 | 1545 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A313-A313 Layman LC; Moffitt DV; McDonough PG; Song M; Shamoun D; Ledbetter DH; Das S Correlation and vertical transmission of fragile X syndrome and ovarian failure within a single family. | 0 | 0 |
| 244 | 0 | 0 | 1546 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A321-A321 Tassone F; Hagerman RJ; Ikle D; Dyer PN; Lampe M; Willemsen R; Oostra BA; Taylor AK FMRP expression as a potential prognostic indicator in fragile X syndrome. | 1 | 1 |
| 245 | 0 | 0 | 1547 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A324-A324 Zhong N; Ju W; Xu WM; Liu B; Dobkin C; Brown WT Molecular pathogenetic studies of the fragile X syndrome: A candidate transcript targeted by the fragile X protein FMRP. | 0 | 0 |
| 246 | 0 | 0 | 1548 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A330-A330 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; Popovich B; Prior TW; Arinami T; Ravine D; Ledbetter DH Methylation analysis of the fragile X syndrome by PCR. | 0 | 0 |
| 247 | 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 |
| 248 | 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 |
| 249 | 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 |
| 250 | 30 | 43 | 1552 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(6):1362-1369 Kenneson A; Cramer DW; Warren ST Fragile X premutations are not a major cause of early menopause | 11 | 22 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 251 | 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 |
| 252 | 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 |
| 253 | 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 |
| 254 | 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 |
| 255 | 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 |
| 256 | 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 |
| 257 | 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 |
| 258 | 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 |
| 259 | 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 |
| 260 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 261 | 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 |
| 262 | 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 |
| 263 | 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 |
| 264 | 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 |
| 265 | 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 |
| 266 | 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 |
| 267 | 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 |
| 268 | 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 |
| 269 | 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 |
| 270 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 271 | 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 |
| 272 | 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 |
| 273 | 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 |
| 274 | 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 |
| 275 | 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 |
| 276 | 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 |
| 277 | 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 |
| 278 | 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 |
| 279 | 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 |
| 280 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 281 | 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 |
| 282 | 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 |
| 283 | 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 |
| 284 | 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 |
| 285 | 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 |
| 286 | 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 |
| 287 | 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 |
| 288 | 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 |
| 289 | 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 |
| 290 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 291 | 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 |
| 292 | 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 |
| 293 | 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 |
| 294 | 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 |
| 295 | 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 |
| 296 | 28 | 40 | 1966 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(2):351-360 Toledano-Alhadef H; Basel-Vanagaite L; Magal N; Davidov B; Ehrlich S; Drasinover V; Taub E; Halpern GJ; Ginott N; Shohat M Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel | 12 | 20 |
| 297 | 18 | 34 | 1967 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(3):504-515 Wohrle D; Salat U; Hameister H; Vogel W; Steinbach P Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells | 4 | 7 |
| 298 | 0 | 0 | 1968 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):177-177 Hagerman RJ; Greco C; Chudley A; Leehey M; Tassone F; Grigsby J; Hills J; Wilson R; Harris SW; Hagerman PJ Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. | 3 | 4 |
| 299 | 0 | 0 | 1969 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):291-291 Thiele H; Peters H; Bahrke D; Hansmann I Homozygosity for a premutation of the FMR1 gene and normal phenotype in two sisters from a family with fragile X syndrome. | 0 | 0 |
| 300 | 0 | 0 | 1970 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):352-352 Gantois I; Reyniers E; Kooy RF Identification of genes differentially expressed in the fragile X syndrome. | 0 | 0 |
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