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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 23: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2201 | 0 | 0 | 1666 1998 HUMAN MUTATION 12(6):432-432 Wang YC; Li SY Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome - Response | 0 | 1 |
| 2202 | 26 | 38 | 1597 1997 HUMAN MUTATION 10(5):393-399 Wang YC; Lin ML; Lin SJ; Li YC; Li SY Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome | 6 | 9 |
| 2203 | 5 | 37 | 1488 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(38):22937-22940 Wang YH; Griffith J Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion | 1 | 22 |
| 2204 | 15 | 21 | 1492 1996 JOURNAL OF MEDICAL GENETICS 33(5):376-378 Wang ZM; Taylor AK; Bridge JA FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 17 | 22 |
| 2205 | 0 | 0 | 2038 2001 JOURNAL OF MEDICAL GENETICS 38:S63-S63 Warburton S; Waters J; Davison V Targeted diagnostic testing for fragile X syndrome | 0 | 0 |
| 2206 | 0 | 0 | 1071 1993 BEHAVIOR GENETICS 23(6):569-569 WARD M; HAY DA COGNITION AND READING-ABILITY IN FRAGILE-X MALES - IS THERE A RELATIONSHIP | 0 | 0 |
| 2207 | 7 | 21 | 549 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):681-688 WARREN ST FRAGILE-X SYNDROME - A HYPOTHESIS REGARDING THE MOLECULAR MECHANISM OF THE PHENOTYPE | 5 | 6 |
| 2208 | 0 | 0 | 1231 1994 JOURNAL OF CELLULAR BIOCHEMISTRY :184-184 WARREN ST OVERVIEW AND UPDATE ON FMR1 AND FRAGILE-X SYNDROME | 0 | 0 |
| 2209 | 5 | 8 | 1588 1997 HOSPITAL PRACTICE 32(4):73-& Warren ST Trinucleotide repetition and fragile X syndrome | 3 | 5 |
| 2210 | 0 | 0 | 1657 1998 FASEB JOURNAL 12(8):A1322-A1322 Warren ST The molecular basis of Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2211 | 70 | 125 | 1304 1995 ANNUAL REVIEW OF NEUROSCIENCE 18:77-99 WARREN ST; ASHLEY CT TRIPLET REPEAT EXPANSION MUTATIONS - THE EXAMPLE OF FRAGILE-X SYNDROME | 24 | 56 |
| 2212 | 6 | 24 | 234 1984 SOMATIC CELL AND MOLECULAR GENETICS 10(4):409-413 WARREN ST; DAVIDSON RL EXPRESSION OF FRAGILE X-CHROMOSOME IN HUMAN RODENT SOMATIC-CELL HYBRIDS | 14 | 19 |
| 2213 | 1 | 15 | 281 1985 HUMAN GENETICS 69(1):44-46 WARREN ST; GLOVER TW; DAVIDSON RL; JAGADEESWARAN P LINKAGE AND RECOMBINATION BETWEEN FRAGILE X-LINKED MENTAL-RETARDATION AND THE FACTOR-IX GENE | 20 | 37 |
| 2214 | 3 | 18 | 731 1990 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 87(10):3856-3860 WARREN ST; KNIGHT SJL; PETERS JF; STAYTON CL; CONSALEZ GG; ZHANG FP ISOLATION OF THE HUMAN CHROMOSOMAL BAND XQ28 WITHIN SOMATIC-CELL HYBRIDS BY FRAGILE X-SITE BREAKAGE | 24 | 69 |
| 2215 | 41 | 81 | 1227 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):536-542 WARREN ST; NELSON DL ADVANCES IN MOLECULAR ANALYSIS OF FRAGILE-X SYNDROME | 59 | 125 |
| 2216 | 4 | 18 | 542 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):613-623 WARREN ST; ZHANG F; SUTCLIFFE JS; PETERS JF STRATEGY FOR MOLECULAR-CLONING OF THE FRAGILE-X SITE DNA | 7 | 12 |
| 2217 | 12 | 37 | 493 1987 SCIENCE 237(4813):420-423 WARREN ST; ZHANG FP; LICAMELI GR; PETERS JF THE FRAGILE-X SITE IN SOMATIC-CELL HYBRIDS - AN APPROACH FOR MOLECULAR-CLONING OF FRAGILE SITES | 29 | 71 |
| 2218 | 5 | 22 | 514 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):115-121 WATSON MS; BREG WR; PAULS D; BROWN WT; CARROLL AJ; HOWARDPEEBLES PN; MERYASH D; SHAPIRO LR ANEUPLOIDY AND THE FRAGILE-X SYNDROME | 6 | 8 |
| 2219 | 6 | 11 | 225 1984 NEW ENGLAND JOURNAL OF MEDICINE 310(22):1462-1462 WATSON MS; LECKMAN JF; ANNEX B; BREG WR; BOLES D; VOLKMAR FR; COHEN DJ; CARTER C FRAGILE X IN A SURVEY OF 75 AUTISTIC MALES | 34 | 56 |
| 2220 | 4 | 8 | 264 1985 CLINICAL GENETICS 27(5):520-521 WEBB GC DETECTION OF THE FRAGILE X-CHROMOSOME AND OTHER FRAGILE SITES | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2221 | 0 | 15 | 70 1982 JOURNAL OF MEDICAL GENETICS 19(1):44-48 WEBB GC; HALLIDAY JL; PITT DB; JUDGE CG; LEVERSHA M FRAGILE (X)(Q27) SITES IN A PEDIGREE WITH FEMALE CARRIERS SHOWING MILD TO SEVERE MENTAL-RETARDATION | 19 | 36 |
| 2222 | 1 | 1 | 27 1981 LANCET 2(8257):1231-1232 WEBB GC; ROGERS JG; PITT DB; HALLIDAY J; THEOBALD T TRANSMISSION OF FRAGILE (X) (Q27) SITE FROM A MALE | 40 | 66 |
| 2223 | 0 | 0 | 1383 1995 NEW SCIENTIST 147(1985):10-10 WEBB J QUESTION MARK HANGS OVER FRAGILE-X TEST IN NEWBORNS | 0 | 0 |
| 2224 | 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 |
| 2225 | 0 | 0 | 711 1990 JOURNAL OF MEDICAL GENETICS 27(3):208-209 WEBB T PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 2226 | 6 | 6 | 870 1991 JOURNAL OF MEDICAL GENETICS 28(12):814-817 WEBB T MOLECULAR-GENETICS OF FRAGILE-X - A CYTOGENETICS VIEWPOINT - REPORT OF THE 5TH INTERNATIONAL-SYMPOSIUM ON X-LINKED MENTAL-RETARDATION, STRASBOURG, FRANCE, 12 TO 16 AUGUST 1991 | 3 | 7 |
| 2227 | 11 | 23 | 893 1991 PRENATAL DIAGNOSIS 11(5):333-338 WEBB T EXPRESSION OF FRAGILE-X IN A FEMALE FETUS DIAGNOSED AFTER CHORIONIC VILLUS SAMPLING | 3 | 4 |
| 2228 | 7 | 15 | 952 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(6):1057-1062 WEBB T DELAYED REPLICATION OF XQ27 IN INDIVIDUALS WITH THE FRAGILE X-SYNDROME | 2 | 16 |
| 2229 | 4 | 4 | 867 1991 JOURNAL OF MEDICAL GENETICS 28(5):358-358 WEBB T; BUNDEY S PREVALENCE OF FRAGILE X-SYNDROME | 5 | 8 |
| 2230 | 15 | 22 | 712 1990 JOURNAL OF MENTAL DEFICIENCY RESEARCH 34:67-73 WEBB T; CRAWLEY P; BUNDEY S FOLATE TREATMENT OF A BOY WITH FRAGILE-X SYNDROME | 2 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2231 | 7 | 21 | 158 1983 PRENATAL DIAGNOSIS 3(2):131-137 WEBB T; GOSDEN CM; RODECK CH; HAMILL MA; EASON PE PRENATAL-DIAGNOSIS OF X-LINKED MENTAL-RETARDATION WITH FRAGILE (X) USING FETOSCOPY AND FETAL BLOOD-SAMPLING | 16 | 32 |
| 2232 | 9 | 16 | 394 1986 JOURNAL OF MEDICAL GENETICS 23(5):400-406 WEBB T; THAKE A; TODD J 12 FAMILIES WITH FRAGILE X(Q27) | 7 | 8 |
| 2233 | 1 | 4 | 221 1984 LANCET 1(8370):220-220 WEBB T; THAKE A; TODD J; BUNDEY S PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 2234 | 5 | 14 | 265 1985 CLINICAL GENETICS 27(6):529-534 WEBB TP CO-CULTIVATION STUDIES IN THE EXPRESSION OF FRAGILE(X) (Q27) IN LYMPHOCYTES | 1 | 2 |
| 2235 | 0 | 0 | 730 1990 PRENATAL DIAGNOSIS 10(8):546-546 WEBB TP RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 2236 | 3 | 3 | 660 1989 PRENATAL DIAGNOSIS 9(11):777-781 WEBB TP; BUNDEY S; MCKINLEY M MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 3 | 5 |
| 2237 | 4 | 11 | 393 1986 JOURNAL OF MEDICAL GENETICS 23(5):396-399 WEBB TP; BUNDEY S; THAKE A; TODD J THE FREQUENCY OF THE FRAGILE X-CHROMOSOME AMONG SCHOOLCHILDREN IN COVENTRY | 68 | 105 |
| 2238 | 0 | 0 | 216 1984 JOURNAL OF MEDICAL GENETICS 21(4):298-298 WEBB TP; BUNDEY SE; THAKE A; TODD J STUDY OF THE FRAGILE X-CHROMOSOME AND MENTAL-RETARDATION | 0 | 3 |
| 2239 | 0 | 0 | 391 1986 JOURNAL OF MEDICAL GENETICS 23(2):166-166 WEBB TP; BUNDEY SE; THAKE A; TODD J THE PREVALENCE OF THE FRAGILE-X SYNDROME IN SCHOOLCHILDREN IN COVENTRY | 0 | 0 |
| 2240 | 12 | 22 | 492 1987 PRENATAL DIAGNOSIS 7(3):203-214 WEBB TP; RODECK CH; NICOLAIDES KH; GOSDEN CM PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME USING FETAL BLOOD AND AMNIOTIC-FLUID | 9 | 18 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2241 | 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 |
| 2242 | 16 | 58 | 1625 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(10):5395-5400 Weiler IJ; Irwin SA; Klintsova AY; Spencer CM; Brazelton AD; Miyashiro K; Comery TA; Patel B; Eberwine J; Greenough WT Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation | 86 | 174 |
| 2243 | 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 |
| 2244 | 34 | 47 | 2022 2001 HUMAN GENETICS 108(6):450-458 Weinhausel A; Haas OA Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR | 2 | 6 |
| 2245 | 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 |
| 2246 | 26 | 45 | 1957 2000 NUCLEIC ACIDS RESEARCH 28(7):1535-1541 Weisman-Shomer P; Cohen E; Fry M Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures | 5 | 11 |
| 2247 | 7 | 58 | 2188 2002 NUCLEIC ACIDS RESEARCH 30(17):3672-3681 Weisman-Shomer P; Cohen E; Fry M Distinct domains in the CArG-box binding factor A destabilize tetraplex forms of the fragile X expanded sequence d(CGG)(n) | 1 | 2 |
| 2248 | 16 | 50 | 2301 2003 NUCLEIC ACIDS RESEARCH 31(14):3963-3970 Weisman-Shomer P; Cohen E; Hershco I; Khateb S; Wolfovitz-Barchad O; Hurley LH; Fry M The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)(n) | 2 | 3 |
| 2249 | 14 | 50 | 1905 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(3):2231-2238 Weisman-Shomer P; Naot Y; Fry M Tetrahelical forms of the fragile X syndrome expanded sequence d(CGG)(n) are destabilized by two heterogeneous nuclear ribonucleoprotein-related telomeric DNA-binding proteins | 5 | 9 |
| 2250 | 5 | 20 | 1517 1996 VARIATION IN THE HUMAN GENOME 197:126-136 Weiss KM; Sutherland GR; Harper PS; Bodmer W; Bowcock AM; Freimer NB; Kidd KK; Chakraborty R; Armour J; Donnelly P; Clark A; Chakravarti A; Weatherall DJ; Edwards JH; Balmain A; Zechner R Unusual inheritance patterns due to dynamic mutation in fragile X syndrome - Discussion | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2251 | 6 | 12 | 329 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):291-296 WELLS TE; MADISON LS ASSESSMENT OF BEHAVIOR-CHANGE IN A FRAGILE-X SYNDROME MALE TREATED WITH FOLIC-ACID | 3 | 5 |
| 2252 | 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 |
| 2253 | 3 | 14 | 1554 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(4):445-449 Wen GY; Jenkins EC; Yao XL; Yoon D; Brown WT; Wisniewski HM Transmission electron microscopy of chromosomes by longitudinal section preparation: Application to fragile X chromosome analysis | 3 | 5 |
| 2254 | 0 | 0 | 406 1986 PEDIATRIC RESEARCH 20(4):A273-A273 WENGER SL; HENNESSEY JC; STEELE MW INCREASED SISTER CHROMATID EXCHANGE (SCE) AT THE FRAGILE X-SITE IN AFFECTED MALES | 0 | 0 |
| 2255 | 8 | 19 | 414 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):909-914 WENGER SL; HENNESSEY JC; STEELE MW INCREASED SISTER CHROMATID EXCHANGE FREQUENCY AT XQ27-SITE IN AFFECTED FRAGILE-X MALES | 5 | 23 |
| 2256 | 26 | 80 | 2189 2002 OBSTETRICS AND GYNECOLOGY CLINICS OF NORTH AMERICA 29(2):367-+ Wenstrom KD Fragile X and other trinucleotide repeat diseases | 1 | 3 |
| 2257 | 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 |
| 2258 | 0 | 0 | 10 1981 ANGLO-WELSH REVIEW (68):6-9 WESTLEY M 'FRAGILE-X' | 0 | 0 |
| 2259 | 0 | 0 | 1572 1997 BRITISH MEDICAL JOURNAL 315(7102):208-208 White C Screening for fragile X is cost effective and accurate | 0 | 0 |
| 2260 | 0 | 0 | 1908 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :98-98 White CD; Menon V; Eliez S; Reiss AL An fMRI study of brain activation in Fragile X Syndrome during a go-nogo task | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2261 | 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 |
| 2262 | 0 | 0 | 1204 1994 CANADIAN FAMILY PHYSICIAN 40:290-295 WIEBE E; WIEBE A FRAGILE-X SYNDROME | 0 | 1 |
| 2263 | 4 | 6 | 1214 1994 GENETIC COUNSELING 5(4):377-380 WIEGERS AM; CURFS LMG; MEIJER H; OOSTRA B; FRYNS JP A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1-GENE CAUSES FRAGILE X-LIKE PSYCHOLOGICAL FEATURES | 0 | 0 |
| 2264 | 4 | 9 | 1064 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 47(2):216-220 WIEGERS AM; CURFS LMG; VERMEER ELMH; FRYNS JP ADAPTIVE-BEHAVIOR IN THE FRAGILE X-SYNDROME - PROFILE AND DEVELOPMENT | 5 | 6 |
| 2265 | 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 |
| 2266 | 15 | 32 | 2186 2002 NEUROPSYCHOLOGIA 40(8):1343-1349 Wilding J; Cornish K; Munir F Further delineation of the executive deficit in males with fragile-X syndrome | 4 | 4 |
| 2267 | 3 | 6 | 1962 2000 PRENATAL DIAGNOSIS 20(10):854-855 Wilkin H; Tuohy J; Theewis W Prenatal diagnosis of fragile X and Turner mosaicism in a 12-week fetus | 1 | 1 |
| 2268 | 0 | 0 | 72 1982 JOURNAL OF MEDICAL GENETICS 19(5):371-371 WILLATT LR; DAVIS J FRAGILE-X MENTAL-RETARDATION IN TWINS - A CASE-HISTORY | 0 | 0 |
| 2269 | 0 | 0 | 1362 1995 JOURNAL OF CELLULAR BIOCHEMISTRY :373-373 WILLEMS PJ; BAKKER CE; REYNIERS E; VERHEIJ C; DEBOULLE K; OOSTRA BA A TRANSGENIC MOUSE MODEL FOR FRAGILE-X SYNDROME | 0 | 0 |
| 2270 | 2 | 5 | 829 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(4):524-524 WILLEMS PJ; VANROY B; RAEYMAEKERS P; OOSTRA B RISK CALCULATIONS IN THE FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2271 | 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 |
| 2272 | 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 |
| 2273 | 7 | 10 | 1608 1997 JOURNAL OF MEDICAL GENETICS 34(3):250-251 Willemsen R; Los F; Mohkamsing S; vandenOuweland A; Deelen W; Galjaard H; Oostra B Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A new appraisal | 10 | 12 |
| 2274 | 8 | 9 | 1377 1995 LANCET 345(8958):1147-1148 WILLEMSEN R; MOHKAMSING S; DEVRIES B; DEVYS D; VANDENOUWELAND A; MANDEL JL; GALJAARD H; OOSTRA B RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME | 73 | 94 |
| 2275 | 12 | 16 | 1935 2000 JOURNAL OF MEDICAL GENETICS 37(8):603-604 Willemsen R; Olmer R; Otero YD; Oostra BA Twin sisters, monozygotic with the fragile X mutation, but with a different phenotype | 7 | 8 |
| 2276 | 3 | 4 | 1499 1996 LANCET 348(9032):967-968 Willemsen R; Oosterwijk JC; Los FJ; Galjaard H; Oostra BA Prenatal diagnosis of fragile X syndrome | 11 | 16 |
| 2277 | 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 |
| 2278 | 38 | 102 | 2351 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):60-67 Willemsen R; Oostra BA; Bassell GJ; Dictenberg J The fragile X syndrome: From molecular genetics to neurobiology | 0 | 0 |
| 2279 | 11 | 15 | 1589 1997 HUMAN GENETICS 99(3):308-311 Willemsen R; Smits A; Mohkamsing S; vanBeerendonk H; deHaan A; deVries B; vandenOuweland A; Sistermans E; Galjaard H; Oostra BA Rapid antibody test for diagnosing fragile X syndrome: A validation of the technique | 34 | 41 |
| 2280 | 18 | 22 | 2283 2003 JOURNAL OF MEDICAL GENETICS 40(5):377-379 Willemsen R; Smits A; Severijnen LA; Jansen M; Jacobs A; De Bruyn E; Oostra B Predictive testing for cognitive functioning in female carriers of the fragile X syndrome using hair root analysis | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2281 | 0 | 0 | 101 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A161-A161 WILLEY A; HATCHER N; HEALY N FRAGILE-X FAMILIES - GENETIC INSTABILITY, OR UNEXPECTED CYTOGENETIC ABERRATIONS | 0 | 0 |
| 2282 | 4 | 11 | 324 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):207-211 WILLIAMS CA; CANTU ES; FRIAS JL BRIEF CLINICAL REPORT - METAPHYSEAL DYSOSTOSIS AND CONGENITAL NYSTAGMUS IN A MALE INFANT WITH THE FRAGILE-X SYNDROME | 2 | 6 |
| 2283 | 3 | 4 | 553 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):733-734 WILSON DP; CARPENTER NJ; BERKOVITZ G THYROID-FUNCTION IN MEN WITH FRAGILE X-LINKED MR | 3 | 3 |
| 2284 | 0 | 1 | 92 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A122-A122 WILSON DP; CARPENTER NJ; BERKOVITZ GD; BROWN TR; MIGEON CJ THYROID-FUNCTION IN FRAGILE X-LINKED MENTAL-RETARDATION | 2 | 2 |
| 2285 | 6 | 16 | 231 1984 PRENATAL DIAGNOSIS 4(1):61-66 WILSON MG; MARCHESE CA PRENATAL-DIAGNOSIS OF FRAGILE-X IN A HETEROZYGOUS FEMALE FETUS AND POSTNATAL FOLLOW-UP | 5 | 9 |
| 2286 | 0 | 0 | 102 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A162-A162 WILSON MG; MARCHESE CA; LIN MS; HERBERT WS; PERDELWITZ M PRENATAL-DIAGNOSIS OF FRAGILE-X IN A HETEROZYGOUS FEMALE FETUS AND POSTNATAL FOLLOW-UP | 0 | 0 |
| 2287 | 9 | 24 | 1130 1993 MENTAL RETARDATION 31(4):221-227 WILSON PG; MAZZOCCO MMM AWARENESS AND KNOWLEDGE OF FRAGILE-X SYNDROME AMONG SPECIAL EDUCATORS | 2 | 3 |
| 2288 | 0 | 0 | 2137 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:323-323 Wilson R; Epstein JH; McKelvie K; Grisgby J; Nagamoto H; Harris S; Reynolds A; Hagerman R Psychological and neuropsychological findings in adults with the premutation and full mutation for Fragile X Syndrome | 0 | 0 |
| 2289 | 0 | 7 | 1442 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):378-381 Wingrove EJ; Norris J; Barton PL; Hagerman R Experiences and attitudes concerning genetic testing and insurance in a Colorado population: A survey of families diagnosed with fragile X syndrome | 0 | 8 |
| 2290 | 10 | 12 | 460 1987 HUMAN GENETICS 77(3):297-298 WINTER R; PEMBREY M INTERPRETATION OF THE HETEROGENEITY IN THE LINKAGE RELATIONSHIPS OF DNA MARKERS AROUND THE FRAGILE-X LOCUS | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2291 | 4 | 7 | 451 1987 HUMAN GENETICS 75(3):269-271 WINTER RM POPULATION-GENETICS IMPLICATIONS OF THE PREMUTATION HYPOTHESIS FOR THE GENERATION OF THE FRAGILE X-MENTAL RETARDATION GENE | 11 | 12 |
| 2292 | 0 | 0 | 471 1987 JOURNAL OF MEDICAL GENETICS 24(4):240-240 WINTER RM POPULATION-GENETICS IMPLICATIONS OF THE PREMUTATION HYPOTHESIS FOR THE GENERATION OF THE FRAGILE-X MENTAL-RETARDATION GENE | 0 | 0 |
| 2293 | 6 | 8 | 626 1989 ARCHIVES OF DISEASE IN CHILDHOOD 64(9):1223-1224 WINTER RM FRAGILE-X MENTAL-RETARDATION | 1 | 3 |
| 2294 | 9 | 16 | 387 1986 HUMAN GENETICS 74(1):93-97 WINTER RM; PEMBREY ME ANALYSIS OF LINKAGE RELATIONSHIPS BETWEEN GENETIC-MARKERS AROUND THE FRAGILE X LOCUS WITH SPECIAL REFERENCE TO THE DAUGHTERS OF NORMAL TRANSMITTING MALES | 13 | 17 |
| 2295 | 1 | 4 | 298 1985 JOURNAL OF MEDICAL GENETICS 22(5):397-397 WINTER RM; PEMBREY ME; DAVIES KE ANALYSIS OF LINKAGE DATA WITH FACTOR-IX CORROBORATES THE HYPOTHESIS THAT A PREMUTATION, FOLLOWED BY A RECOMBINATION EVENT, GENERATES THE FULL MUTATION IN FRAGILE X-LINKED MENTAL-RETARDATION | 2 | 2 |
| 2296 | 13 | 39 | 1910 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(4):278-282 Wisbeck JM; Huffman LC; Freund L; Gunnar MR; Davis EP; Reiss AL Cortisol and social stressors in children with fragile X: A pilot study | 8 | 10 |
| 2297 | 9 | 47 | 255 1985 ANNALS OF NEUROLOGY 18(6):665-669 WISNIEWSKI KE; FRENCH JH; FERNANDO S; BROWN WT; JENKINS EC; FRIEDMAN E; HILL AL; MIEZEJESKI CM FRAGILE X-SYNDROME - ASSOCIATED NEUROLOGICAL ABNORMALITIES AND DEVELOPMENTAL-DISABILITIES | 27 | 43 |
| 2298 | 0 | 0 | 1053 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1513-1513 WITTWER B; ZYGULSKA M; MINY P; EIGEL A; HORST J TESTING FOR FRAGILE X-SYNDROME IN 120 FAMILIES WITH A HISTORY OF MENTAL-RETARDATION | 0 | 0 |
| 2299 | 24 | 65 | 706 1990 HUMAN GENETICS 85(6):659-665 WOHRLE D; FRYNS JP; STEINBACH P FRAGILE-X EXPRESSION AND FRAGILE-X INACTIVATION .1. THE EXPRESSION OF THE FRAGILE SITE AT XQ27.3 IS NOT SUPPRESSED ON INACTIVE X-CHROMOSOMES SEPARATED FROM THE ACTIVE HOMOLOG | 7 | 9 |
| 2300 | 19 | 23 | 1136 1993 NATURE GENETICS 4(2):140-142 WOHRLE D; HENNIG I; VOGEL W; STEINBACH P MITOTIC STABILITY OF FRAGILE-X MUTATIONS IN DIFFERENTIATED CELLS INDICATES EARLY POSTCONCEPTIONAL TRINUCLEOTIDE REPEAT EXPANSION | 58 | 120 |
Page 23: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
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