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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by GCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1801 | 0 | 0 | 105 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 |
| 1802 | 0 | 1 | 118 1983 BIOLOGY OF THE CELL 48(2-3):A92-A92 LENOARD C; SCHOEVAERT D; SELVA J APPLICATION OF THE AUTOMATIC-ANALYSIS OF METAPHASES TO THE DIAGNOSIS OF THE FRAGILE-X IN MAN | 0 | 0 |
| 1803 | 0 | 0 | 120 1983 CLINICAL GENETICS 23(3):216-216 MCDERMOTT A MORE ON THE FRAGILE-X, WITH PARTICULAR REFERENCE TO FIBROBLAST AND AMNIOTIC-FLUID CULTURE, AND X-INACTIVATION | 0 | 0 |
| 1804 | 0 | 1 | 134 1983 CLINICAL RESEARCH 31(2):A290-A290 BROWN T; JENKINS E; FRIEDMAN E; BROOKS J; DUNCAN C; et al. FOLIC-ACID THERAPY OF FRAGILE-X SYNDROME | 0 | 0 |
| 1805 | 0 | 1 | 135 1983 CLINICAL RESEARCH 31(5):A897-A897 HOWARDPEEBLES PN NORMAL-MALE TRANSMISSION OF THE FRAGILE-X - THE COUNSELING DILEMMA | 0 | 0 |
| 1806 | 3 | 10 | 143 1983 JOURNAL DE GENETIQUE HUMAINE 31(2):133-139 JALBERT H; BAETEMAN MA; TROCHETROYER C; MATTEI MG; MATTEI JF; et al. MENTAL-RETARDATION WITH FRAGILE-X - NEITHER INACTIVATION NOR DELETION OF THE SEGMENT Q28-]Q TER ENZYMATIC AND MORPHOMETRIC DATA | 0 | 0 |
| 1807 | 3 | 9 | 149 1983 JOURNAL OF MEDICAL GENETICS 20(4):314-315 HUNTER AGW; MACDONALD J; EVANS JA ABSENCE OF THE FRAGILE-X IN A GROUP OF PATIENTS WITH IDIOPATHIC MENTAL-RETARDATION | 0 | 0 |
| 1808 | 0 | 0 | 155 1983 MEDICINA-BUENOS AIRES 43(6):756-756 DELREY G; COCO R INVESTIGATION OF FRAGILE X-CHROMOSOMES IN MEN WITH MENTAL-RETARDATION (RM) OF UNKNOWN CAUSE | 0 | 0 |
| 1809 | 0 | 0 | 159 1983 PATHOLOGY 15(1):105-106 JACKY PB; SUTHERLAND GR FRAGILE-X EXPRESSION IN FIBROBLASTS | 0 | 0 |
| 1810 | 6 | 26 | 163 1983 REVISTA MEDICA DE CHILE 111(6):597-600 SANTOS M; MORIZON G THE FRAGILE X SYNDROME - A CHROMOSOMAL DEFECT ASSOCIATED WITH MENTAL-RETARDATION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1811 | 0 | 0 | 169 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(3):322-322 MIXON JC INHIBITION OF FRAGILE-X EXPRESSION BY 5-AZACYTIDINE (AZA) AND BY S-ADENOSYLHOMOCYSTEINE (SAH) | 0 | 0 |
| 1812 | 0 | 2 | 189 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(4):857-858 CHUDLEY AE; KNOLL JH; GERRARD JW FRAGILE-X MALES WITH NORMAL INTELLIGENCE - AND IF SO, WHY - REPLY | 0 | 0 |
| 1813 | 0 | 0 | 198 1984 CLINICAL RESEARCH 32(5):A884-A884 FRIEDMAN JM; HOWARDPEEBLES PN A THEORETICAL-MODEL FOR UNAFFECTED CARRIER MALES IN FRAGILE-X FAMILIES | 0 | 0 |
| 1814 | 0 | 0 | 199 1984 CLINICAL RESEARCH 32(5):A885-A885 HOLMAN GH; ALLEN SM; TUCKER DA; TAWATER BA SEIZURES AND UNUSUAL VISUAL EVOKED-RESPONSES IN FRAGILE-X CARRIERS | 0 | 0 |
| 1815 | 0 | 0 | 200 1984 CYTOGENETICS AND CELL GENETICS 37(1-4):432-432 CAMERINO G; MATTEI MG; MATTEI JF; JAYE M; MANDEL JL CLOSE LINKAGE BETWEEN THE LOCI FOR THE FRAGILE X MENTAL-RETARDATION AND HEMOPHILIA-B | 0 | 0 |
| 1816 | 0 | 0 | 202 1984 EMERGENCY MEDICINE 16(15):103-& [Anon] IN SEARCH OF THE FRAGILE-X | 0 | 0 |
| 1817 | 0 | 0 | 209 1984 IRISH JOURNAL OF MEDICAL SCIENCE 153(1):29-30 DEARCE MA; LAW E A SIMPLE STATISTICAL APPROACH TO AVOID FALSE POSITIVES IN THE CYTOGENETIC DIAGNOSIS OF FRAGILE X-CHROMOSOMES | 0 | 0 |
| 1818 | 0 | 0 | 210 1984 JAPANESE JOURNAL OF GENETICS 59(6):618-619 HORI T; AYUSAWA D; SENO T EXPRESSION OF THE FRAGILE X-CHROMOSOME UNDER CONDITIONS OF THYMIDYLATE STRESS | 0 | 0 |
| 1819 | 0 | 1 | 215 1984 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 5(3):160-161 DESPOSITO F THE FRAGILE X-SYNDROME - DIAGNOSIS, BIOCHEMISTRY AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 1820 | 0 | 1 | 229 1984 NEW ENGLAND JOURNAL OF MEDICINE 310(22):1471-1471 STEIN M THE FRAGILE X SYNDROME - DIAGNOSIS, BIOCHEMISTRY, AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1821 | 0 | 0 | 231 1984 PATHOLOGY 16(1):108-108 SUTHERLAND GR THE FRAGILE X-CHROMOSOME | 0 | 0 |
| 1822 | 0 | 0 | 232 1984 PATHOLOGY 16(1):108-108 THEOBALD TM; HAY DA INDIVIDUAL VARIATION AND SPECIFIC COGNITIVE DEFICITS IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 1823 | 1 | 26 | 240 1985 AMERICAN JOURNAL OF DANCE THERAPY 8:67-80 WOLFSCHEIN EG; FISCH GS; COHEN IL A STUDY OF THE USE OF NONVERBAL SYSTEMS IN THE DIFFERENTIAL-DIAGNOSIS OF AUTISTIC, MENTALLY-RETARDED AND FRAGILE X-INDIVIDUALS | 0 | 0 |
| 1824 | 0 | 1 | 253 1985 AMERICAN JOURNAL OF MENTAL DEFICIENCY 89(4):448-448 CROCKER AC THE FRAGILE X-SYNDROME - DIAGNOSIS, BIOCHEMISTRY, AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 1825 | 0 | 0 | 261 1985 CLINICAL CHEMISTRY 31(6):1008-1009 THIBODEAU SN; FAULK KR; SMITH AC; BERRY R; HAGERMAN R THE USE OF RECOMBINANT DNA TECHNIQUES TO DOCUMENT THE TRANSMISSION OF FRAGILE-X SYNDROME THROUGH AN UNAFFECTED MALE CARRIER | 0 | 0 |
| 1826 | 0 | 0 | 271 1985 CLINICAL GENETICS 28(5):422-423 DAVIES KE; OLD J; MCGLADE S; SPEER A; COUTELLE C; et al. LINKAGE OF RFLPS AROUND THE DMD AND BMD LOCI AND THE FRAGILE X-LOCUS | 0 | 0 |
| 1827 | 0 | 0 | 272 1985 CLINICAL GENETICS 28(5):449-449 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; et al. FRAGILE X-SYNDROME AND MENTAL-RETARDATION IN GREECE | 0 | 0 |
| 1828 | 2 | 5 | 273 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):606-606 CONNOR JM; COLGAN JM; CROSSLEY JA; IMRIE SJ; YATES JRW; et al. MULTIPOINT LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE X-SYNDROME AND FAMILIES WITH HEMOPHILIA-B | 0 | 0 |
| 1829 | 1 | 5 | 274 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):612-612 DAVIES KE; HARPER K; MATTEI MG; MATTEI JF; VEENEMA H; et al. LINKAGE RELATIONSHIP OF DNA SEGMENT 52A (HGM7-DXS51) AND FACTOR-IX (HGM7-F9) TO FRAGILE-X MENTAL-RETARDATION (FRAXQ27) | 0 | 0 |
| 1830 | 0 | 0 | 275 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):645-645 GOONEWARDENA P; TOLUN A; GUSTAVSON KH; HOLMGREN G; LINDSTEN J; et al. STUDIES ON THE FRAGILE-X MENTAL-RETARDATION SYNDROME, DUCHENNE MUSCULAR-DYSTROPHY AND X-LINKED RETINITIS PIGMENTOSA IN SWEDISH FAMILIES, BY THE USE OF DNA PROBES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1831 | 1 | 2 | 279 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):788-788 ZOLL B; ARNEMANN J; KRAWCZAK M; COOPER DN; PESCIA G; et al. THE LOCI FOR FRAGILE X-MENTAL RETARDATION SYNDROME AND COAGULATION FACTOR-IX ARE NOT CLOSELY LINKED | 0 | 0 |
| 1832 | 0 | 0 | 280 1985 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 27(1):95-96 PUESCHEL SM; FINELLI PV NEUROLOGICAL INVESTIGATIONS IN PATIENTS WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1833 | 0 | 0 | 294 1985 JAPANESE JOURNAL OF HUMAN GENETICS 30(2):150-150 IKEDA T; MIYAGI C; HIRAYAMA K FRAGILE X-SYNDROME - REPORT OF 2 FAMILIES AND CYTOGENETIC STUDIES | 0 | 0 |
| 1834 | 0 | 3 | 298 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 LAWRENCE RJ THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME | 0 | 0 |
| 1835 | 1 | 1 | 305 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(2):240-240 SHELL J; CAMPBELL M AUTISM OR FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 1836 | 0 | 1 | 306 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(5):673-674 SZYMANSKI LS THE FRAGILE-X SYNDROME - DIAGNOSIS, BIOCHEMISTRY AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 1837 | 0 | 0 | 309 1985 NEUROPEDIATRICS 16(3):171-172 GRANSTROM ML; SIMOLA KOJ; YLINEN A; RINTAHAKA P THE FRAGILE-X SYNDROME IN CHILDHOOD - A THERAPEUTIC TRIAL WITH FOLIC-ACID | 0 | 0 |
| 1838 | 0 | 0 | 310 1985 PEDIATRIC RESEARCH 19(4):A253-A253 ROSENBLATT DS; ZEESMAN SF; VEKEMANS MJJ; DUSCHENES EA; HELLSTROM FV; et al. FOLIC-ACID BLINDED TRIAL IN IDENTICAL-TWINS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1839 | 4 | 11 | 312 1985 SEMAINE DES HOPITAUX 61(25):1807-1809 LEJEUNE J; RETHORE MO; DEBLOIS MC; RAVEL A ASSAY OF FOLIC-ACID TREATMENT IN FRAGILE-X SYNDROME | 0 | 0 |
| 1840 | 0 | 0 | 315 1986 ACTA NEUROLOGICA SCANDINAVICA 73(4):447-448 BAKKE JV FRAGILE-X SYNDROME AS A CONCOMITANT TO AND PROBABLE CAUSE OF MENTAL-RETARDATION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1841 | 0 | 0 | 359 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 25(1):188-188 SHABTAI F; KLAR D; HART J; HALBRECHT I FRAGILE-X SYNDROME - A GENETIC OR AN INFECTIOUS-DISEASE | 0 | 0 |
| 1842 | 0 | 0 | 366 1986 ARCHIVOS DE BIOLOGIA Y MEDICINA EXPERIMENTALES 19(1):R133-R133 LACASSIE Y; MORENO R; ALLIENDE MA; DELABARRA F; BARAHONA G; et al. LACK OF EFFECT OF FOLIC-ACID THERAPY ON MENTAL RETARDED PATIENTS WITH FRAGILE-X OR OTHER AUTOSOMAL FRAGILITIES IN A DOUBLE-BLIND-STUDY | 0 | 0 |
| 1843 | 0 | 0 | 367 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(3):237-237 TURNER G; LAING S; ROBINSON H; PURVISSMITH S A PROGRAM FOR PRIMARY PREVENTION OF INTELLECTUAL HANDICAP - FRAGILE (X) SCREENING | 0 | 0 |
| 1844 | 0 | 0 | 368 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):350-350 LOESCH DZ; HAY D PHENOTYPIC DIVERSITY OF FRAGILE-X FEMALES AND ITS GENETIC-IMPLICATIONS | 0 | 0 |
| 1845 | 0 | 0 | 369 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):352-352 MULLEY JC; THORN K; SUTHERLAND GR LINKAGE RELATIONSHIPS OF THE FRAGILE-X | 0 | 0 |
| 1846 | 0 | 0 | 370 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):356-356 SUTHERLAND GR; BAKER E INDUCTION OF THE FRAGILE-X IN FIBROBLASTS BY THYMIDINE | 0 | 0 |
| 1847 | 0 | 0 | 371 1986 BIOPHYSICAL JOURNAL 49(2):A18-A18 STUTZIN A; POLLARD HB SYNEXIN-INDUCED FUSION OF CHROMAFFIN GRANULE GHOSTS (CGG) STUDIED BY A NOVEL FLUORESCENCE ASSAY | 0 | 0 |
| 1848 | 2 | 6 | 373 1986 BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE 102(12):1742-1745 ZAKHAROV AF; BEDELBAEVA KA; BARANOVSKAYA LI VARIABILITY OF FRAGILE X-CHROMOSOME EXPRESSION IN CONSECUTIVE CELL GENERATIONS | 0 | 0 |
| 1849 | 0 | 0 | 375 1986 CLINICAL CHEMISTRY 32(6):1215-1215 THIBODEAU SN THE USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS (RFLP) TO DETERMINE THE CARRIER STATUS OF FRAGILE-X-SYNDROME | 0 | 0 |
| 1850 | 0 | 0 | 383 1986 CLINICAL RESEARCH 34(1):A34-A34 VANDYKE DL; WEISS L MATERNAL EFFECT ON INTELLIGENCE IN FRAGILE-X MALES AND FEMALES - AN HYPOTHESIS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1851 | 0 | 0 | 384 1986 CLINICAL RESEARCH 34(1):A114-A114 LOEHR JP; SYNHORST DP; HAGERMAN RJ; WOLFE RR CARDIOVASCULAR-ABNORMALITIES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1852 | 0 | 1 | 388 1986 FEDERATION PROCEEDINGS 45(3):702-702 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE X EXPRESSION IN THE PRESENCE OF 5-FLUORO-2'-DEOXYURIDINE (FUDR) | 0 | 0 |
| 1853 | 0 | 0 | 392 1986 JAPANESE JOURNAL OF HUMAN GENETICS 31(2):150-150 ARINAMI T; TAKANAWA S; KONDO I THE FRAGILE X-SYNDROME IN A JAPANESE POPULATION OF INSTITUTIONALIZED MENTALLY-RETARDED MALES | 0 | 0 |
| 1854 | 0 | 0 | 393 1986 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 7(3):201-202 LACHIEWICZ AM; GULLION CM; SPIRIDIGLIOZZI GA; ALYSWORTH AS DECLINE IN IQ SCORES OF YOUNG FRAGILE X-MALES | 0 | 0 |
| 1855 | 0 | 0 | 395 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 |
| 1856 | 0 | 0 | 396 1986 JOURNAL OF MEDICAL GENETICS 23(2):166-167 CONNOR JM; COLGAN JM; CROSSLEY JA; IMRIE SJ; YATES JRW MULTIPOINT LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE-X SYNDROME | 2 | 0 |
| 1857 | 5 | 12 | 404 1986 LANCET 2(8517):1191-1192 [Anon] PREVENTIVE SCREENING FOR FRAGILE-X SYNDROME | 3 | 0 |
| 1858 | 0 | 0 | 410 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 |
| 1859 | 0 | 0 | 412 1986 RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS 12(4):442-444 DELGIUDICE E; POGGI V; SARTORIO R; CARROZZO R; ROMANO A; et al. THE FRAGILE X-SYNDROME | 0 | 0 |
| 1860 | 0 | 0 | 429 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):75-75 LOESCH DZ DERMATOGLYPHIC ABNORMALITY IN FRAGILE X-SYNDROME - A NEW CAUSAL HYPOTHESIS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1861 | 0 | 0 | 430 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):79-79 GEDEON AK; MULLEY JC; SUTHERLAND GR LINKAGE ANALYSIS AND CARRIER DETECTION OF THE FRAGILE-X | 0 | 0 |
| 1862 | 0 | 0 | 431 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):81-81 SUTHERLAND GR; BAKER E; HOCKEY A; PURVISSMITH S THE USE OF THYMIDINE INDUCTION OF THE FRAGILE X-CHROMOSOME IN PRENATAL-DIAGNOSIS | 0 | 0 |
| 1863 | 0 | 0 | 432 1987 BEHAVIOR GENETICS 17(6):642-642 VANDENBERG SG A STATUS-REPORT ON THE FRAGILE X-SYNDROME | 0 | 0 |
| 1864 | 0 | 0 | 439 1987 CLINICAL RESEARCH 35(1):A60-A60 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE-X (FRA-X) EXPRESSION IN THE PRESENCE OF 5-FLOURO-2'-DEOXYURIDINE (FDUMP) | 0 | 0 |
| 1865 | 0 | 0 | 440 1987 CLINICAL RESEARCH 35(1):A60-A60 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| 1866 | 0 | 0 | 441 1987 CLINICAL RESEARCH 35(1):A211-A211 HAGERMAN RJ; JACKSON AW; BERRY R; CAMPBELL J; STILLMAN E; et al. PREDICTORS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1867 | 0 | 0 | 445 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):594-594 CLAYTON JF; GOSDEN CM; HASTIE N; EVANS HJ MULTIPOINT ANALYSIS AND FRAGILE-X | 0 | 0 |
| 1868 | 0 | 0 | 447 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):622-622 GOSDEN C; BUCHANAN J; NEWTON M; KESTON M; WRIGHT AF; et al. FRAGILE-X SYNDROME - NEW LINKAGE DATA IN 10 FAMILIES | 0 | 0 |
| 1869 | 0 | 0 | 449 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):690-690 SENIOR J; KILPATRICK M; WEBB T LINKAGE STUDIES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1870 | 1 | 2 | 453 1987 HASTINGS CENTER REPORT 17(1):2-3 [Anon] TO SCREEN OR NOT TO SCREEN FOR THE FRAGILE X-SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1871 | 0 | 0 | 465 1987 INTERNATIONAL JOURNAL OF NEUROSCIENCE 34(3-4):172-172 FERRI R; BERGONZI P; COLOGNOLA RM; MUSUMECI SA; PETRELLA MA; et al. BRAIN-STEM AUDITORY AND VISUAL EVOKED-POTENTIALS IN FRAGILE-X MENTAL-RETARDATION SYNDROME SUBJECTS | 0 | 0 |
| 1872 | 0 | 0 | 466 1987 JAPANESE JOURNAL OF GENETICS 62(6):520-520 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M STRUCTURAL ALTERATION IN FRA(X)(Q27.3) ASSOCIATED WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1873 | 0 | 0 | 467 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):122-123 SUGIO Y FRAGILE-X SYNDROME - COLLABORATIVE STUDIES OF JAPANESE PATIENTS | 0 | 0 |
| 1874 | 0 | 0 | 468 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):170-171 ARINAMI T; NAKAJIMA S; KONDO I THE FRAGILE X-SYNDROME IN A JAPANESE POPULATION OF INSTITUTIONALIZED MENTALLY-RETARDED FEMALES | 0 | 0 |
| 1875 | 0 | 0 | 469 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):171-171 KASAI R; NARAHARA K; MURAKAMI M; KIKKAWA K; KIMURA S; et al. PREVALENCE OF THE FRAGILE(X) SYNDROME IN INSTITUTIONALIZED MENTALLY-RETARDED INDIVIDUALS | 0 | 0 |
| 1876 | 0 | 0 | 470 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):210-211 ARINAMI T; TAMURA K; KONDO I A FRAGILE X-FEMALE WITH DOWN-SYNDROME - A CASE-REPORT | 0 | 0 |
| 1877 | 0 | 0 | 475 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 |
| 1878 | 4 | 5 | 485 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(6):938-938 HAGERMAN RJ FRAGILE-X CHROMOSOME AND LEARNING-DISABILITY | 0 | 0 |
| 1879 | 0 | 0 | 493 1987 PEDIATRIC RESEARCH 21(4):A230-A230 SHAPIRO LR; WILMOT PL; OMAR RA; DAVIDIAN MM; CHANDER PN PRENATAL PATHOGENESIS OF MACROORCHIDISM IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 1880 | 0 | 0 | 504 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-20 KAHKONEN M; ALITALO T; AIRAKSINEN E; MATILAINER R; LAUNIALA K; et al. PREVALENCE OF THE FRAGILE-X OR MARTIN-BELL SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1881 | 0 | 0 | 506 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):21-21 LEDBETTER DH; LEDBETTER SA HIGH-LEVELS OF FRAGILE-X EXPRESSION IN NORMAL MALES INDUCED BY APHIDICOLIN | 0 | 0 |
| 1882 | 0 | 0 | 507 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):22-22 LEISTI J; KAHKONEN M; HERVA R; WINQVIST R; UKKOLA L; et al. THE FRAGILE-X SYNDROME IN NORTHERN FINLAND - A GENEALOGIC STUDY | 0 | 0 |
| 1883 | 0 | 0 | 508 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):22-23 OBERLE I; ARVEILER B; WOELFLIN A; HOFKER M; PEARSON P; et al. GENETIC AND PHYSICAL MAPPING OF THE FRAGILE-X REGION - .A. NEW POLYMORPHIC MARKERS .B. IS THE FRAGILE-X SITE A PREFERENTIAL BREAKPOINT IN CHROMOSOME REARRANGEMENTS | 0 | 0 |
| 1884 | 0 | 0 | 509 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):23-24 RUDELLI R; MADRID R; BROWN WT FURTHER NEUROPATHOLOGICAL OBSERVATIONS IN ADULT FRAGILE-X | 0 | 0 |
| 1885 | 0 | 0 | 511 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):26-26 TOMMERUP N; TRANEBJAERG L; TONNESEN T; KASTERN W; HANSEN H; et al. IDENTICAL EXPRESSION OF THE FRAGILE-X BUT DISCORDANT CLINICAL MANIFESTATIONS IN MONOZYGOTIC TWINS WITH MARTIN-BELL SYNDROME | 0 | 0 |
| 1886 | 0 | 0 | 512 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):26-27 TURNER G; PARTINGTON MW; ROBINSON H; LATHAM M; KENNY J; et al. THE PROS AND CONS OF PREVENTIVE SCREENING FOR THE FRAGILE (X) | 0 | 0 |
| 1887 | 5 | 12 | 561 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):775-778 BUTLER MG; DEV VG; SHAH D; ULM JE; WILMOT PL; et al. THE USE OF EARLY SIMULTANEOUS PERCUTANEOUS UMBILICAL BLOOD-SAMPLING (PUBS) AND AMNIOCENTESIS FOR PRENATAL FRAGILE-X CHROMOSOME DIAGNOSIS | 0 | 0 |
| 1888 | 0 | 0 | 565 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):91-91 TURNER G ISSUES ARISING FROM FRAGILE-X PREVENTIVE SCREENING | 0 | 0 |
| 1889 | 0 | 0 | 566 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):91-91 LAING S; LATHAM M; KENNY J; PURVISSMITH S; TURNER G CYTOGENETIC ANOMALIES IN A POPULATION SELECTED FOR FRAGILE-X SCREENING | 0 | 0 |
| 1890 | 0 | 0 | 567 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):93-94 GARRY MB; MACFARLANE SC; PULLON DHH FRAGILE-X POSITIVE TURNERS MOSAIC | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1891 | 0 | 0 | 568 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):96-96 PURVISSMITH S; LAING S; STEWART L; TURNER G; WASS D; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X | 0 | 0 |
| 1892 | 0 | 2 | 569 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):97-97 SUTHERS GK; THODE A; TURNER GL CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS | 0 | 0 |
| 1893 | 0 | 0 | 577 1988 CLINICAL GENETICS 33(6):464-464 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 0 | 0 |
| 1894 | 0 | 0 | 579 1988 CLINICAL RESEARCH 36(1):A207-A207 BIXENMAN H; HECHT F; LOCKWOOD D; HECHT BK NEW COMMON FRAGILE SITE AT XQ27.3 CONFOUNDED WITH FRAGILE-X | 0 | 0 |
| 1895 | 1 | 2 | 585 1988 HUMAN GENETICS 78(2):196-197 SUBRT I; STIRSKA K FREQUENCY OF TRIRADIAL AND MULTIRADIAL CONFIGURATIONS IN FRAGILE X-CHROMOSOMES | 0 | 0 |
| 1896 | 0 | 0 | 595 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):224-224 ARINAMI T; SATO M; KONDO I AUDITORY BRAIN-STEM RESPONSES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1897 | 0 | 0 | 596 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):225-225 KONDO I; ARINAMI T PREVALENCE OF CHROMOSOME-ANOMALIES IN MENTALLY-RETARDED SCHOOL-CHILDREN - STUDY OF POPULATION INCIDENCE OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1898 | 0 | 0 | 597 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):245-245 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M EXPRESSION OF FRA(X)(Q27.3) ASSOCIATED WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1899 | 0 | 1 | 600 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):457-458 WOLFSCHEIN EG; JENKINS EC; SKLOWER S; COHEN IL; WISNIEWSKI KE; et al. ON THE ASSOCIATION OF FRAGILE-X WITH AUTISM | 0 | 0 |
| 1900 | 0 | 0 | 601 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):458-458 SCHOPLER E ON THE ASSOCIATION OF FRAGILE-X WITH AUTISM - RESPONSE | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1901 | 1 | 1 | 605 1988 JOURNAL OF MEDICAL GENETICS 25(1):64-64 LACA Z; BRANKOVIC S EXPRESSION OF FRAGILE X-CHROMOSOME AND POSSIBLE DELETION IN SUCCESSIVE CELL DIVISIONS | 0 | 0 |
| 1902 | 0 | 0 | 606 1988 JOURNAL OF MEDICAL GENETICS 25(2):128-128 ENGLISH C ANTHROPOMETRIC STUDIES IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 1903 | 0 | 0 | 607 1988 JOURNAL OF MEDICAL GENETICS 25(2):129-129 DAVIES KE; PATTERSON M; BELL M; KENWRICK SJ MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 1904 | 0 | 0 | 608 1988 JOURNAL OF MEDICAL GENETICS 25(2):131-131 MCKINLEY MJ; KEARNEY LU; NICOLAIDES K PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY PLACENTAL BIOPSY | 0 | 0 |
| 1905 | 0 | 0 | 610 1988 NEUROTOXICOLOGY 9(1):139-140 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| 1906 | 2 | 7 | 619 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):978-979 ARINAMI T BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 1907 | 0 | 0 | 626 1989 AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 78(2):200-200 BUTLER MG; HAYNES JL; ALLEN GA; SINGH DN ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT FRAGILE X-SYNDROME | 0 | 0 |
| 1908 | 2 | 17 | 631 1989 ARCHIVES OF NEUROLOGY 46(12):1269-1270 GRIGSBY J; HAGERMAN R FRAGILE-X SYNDROME - A GENETIC ETIOLOGY FOR DEVELOPMENTAL GERSTMANN SYNDROME | 0 | 0 |
| 1909 | 0 | 0 | 636 1989 CLINICAL RESEARCH 37(1):A170-A170 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; et al. LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 0 | 0 |
| 1910 | 0 | 1 | 651 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(4):643-643 LACHIEWICZ AM FRAGILE-X SYNDROME - A HANDBOOK FOR FAMILIES AND EDUCATORS - FINUCANE,B | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1911 | 0 | 1 | 661 1989 NATURE 341(6243):580-580 HARRIS A; BOBROW M THE FRAGILE-X SYNDROME - DAVIES,KE | 0 | 0 |
| 1912 | 0 | 0 | 664 1989 PEDIATRIC RESEARCH 25(4):A16-A16 MERYASH DL PERCEPTION OF BURDEN AMONG AT-RISK WOMEN OF RAISING A CHILD WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1913 | 0 | 0 | 668 1989 REVISTA BRASILEIRA DE GENETICA 12(2):391-404 NAVAJAS L; VIANNAMORGANTE AM RELATIONSHIP BETWEEN AGE AND MENTAL STATUS AND THE EXPRESSION OF THE FRAGILE(X) IN HETEROZYGOTES FOR THE MARTIN-BELL SYNDROME | 0 | 0 |
| 1914 | 1 | 2 | 687 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):433-433 MEISNER LF FRAGILE-X FREQUENCY | 0 | 0 |
| 1915 | 1 | 1 | 688 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):434-434 MINGRONINETTO RC; ROSENBERG C; VIANNAMORGANTE AM; PAVANELLO RCM FRAGILE-X FREQUENCY - RESPONSE | 0 | 0 |
| 1916 | 2 | 6 | 689 1990 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 163(5):1713-1714 SINDWANI V; VERMA RS CYTOGENETIC UNCERTAINTIES SURROUNDING THE FRAGILE X IN MARTIN-BELL SYNDROME | 0 | 0 |
| 1917 | 8 | 13 | 692 1990 ANNALES DE GENETIQUE 33(2):109-110 LUCOTTE G A NEW DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1918 | 0 | 0 | 693 1990 ANNALS OF NEUROLOGY 28(3):440-440 BERRYKRAVIS E; HUTTENLOCHER PR CYCLIC-AMP METABOLISM IN FRAGILE X-SYNDROME | 0 | 0 |
| 1919 | 1 | 40 | 694 1990 ARCHIVES FRANCAISES DE PEDIATRIE 47(10):701-703 PIUSSAN C X-LINKED MENTAL-RETARDATION WITHOUT FRAGILE X-CHROMOSOME | 0 | 0 |
| 1920 | 2 | 14 | 698 1990 BRITISH DENTAL JOURNAL 168(4):160-162 NUNN JH; DURNING P FRAGILE-X (MARTIN BELL) SYNDROME AND DENTAL-CARE | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1921 | 0 | 0 | 703 1990 CLINICAL RESEARCH 38(1):A164-A164 HAGERMAN R; AMIRI K; CRONISTER A; WITTENBERGER M; SCHREINER R; et al. FRAGILE-X GIRLS - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 0 | 0 |
| 1922 | 10 | 27 | 705 1990 EUROPEAN NEUROLOGY 30(1):32-37 RAIMONDI E; LENTI C; ROMAGNONI M; NEGRI R; GAMBINI E; et al. FRAGILE-X MENTAL-RETARDATION IN A LARGE 5-GENERATION FAMILY - A CLINICAL AND CYTOGENETIC STUDY | 0 | 0 |
| 1923 | 5 | 7 | 709 1990 HUMAN GENETICS 85(1):141-142 SUTHERS GK; SUTHERLAND GR RECOMBINATION AND THE FRAGILE-X | 0 | 0 |
| 1924 | 0 | 1 | 714 1990 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 31(7):1165-1166 BOLTON P THE FRAGILE X-SYNDROME - DAVIES,K | 0 | 0 |
| 1925 | 0 | 0 | 716 1990 JOURNAL OF MEDICAL GENETICS 27(3):208-208 GLASS IA; WHITE EM; PIRRIT LA; BELL MV; CONNOR JM LINKAGE STUDY OF F8 IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1926 | 0 | 0 | 717 1990 JOURNAL OF MEDICAL GENETICS 27(3):208-209 WEBB T PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1927 | 3 | 7 | 719 1990 JOURNAL OF MENTAL DEFICIENCY RESEARCH 34:81-86 COLLACOTT RA; DUCKETT DP; MATHEWS D; WARRINGTON JS; YOUNG ID DOWNS-SYNDROME AND FRAGILE-X SYNDROME IN A SINGLE PATIENT | 0 | 0 |
| 1928 | 5 | 11 | 723 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(1):1-2 GOODYEAR HM; SONKSON PM FRAGILE X-SYNDROME - AN IMPORTANT CAUSE OF MENTAL-RETARDATION | 0 | 0 |
| 1929 | 0 | 1 | 724 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(6):415-415 HALSTEAD S FRAGILE X-SYNDROME | 0 | 0 |
| 1930 | 0 | 0 | 725 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(6):415-415 GOODYEAR HM; SONKSON PM FRAGILE X-SYNDROME - REPLY | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1931 | 0 | 0 | 733 1990 PEDIATRIC RESEARCH 27(4):A12-A12 LACHIEWICZ AM; SPIRIDIGLIOZZI GA; GULLION CA; RANSFORD SK ABERRANT BEHAVIORS OF YOUNG BOYS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1932 | 0 | 0 | 734 1990 PEDIATRIC RESEARCH 27(4):A136-A136 SHAPIRO LR; WILMOT PL SPONTANEOUS FRAGILE-X CHROMOSOMES IN ROUTINE AMNIOTIC-FLUID CULTURE - THE X-CHROMOSOME COMMON FRAGILE SITE [(X) (Q27.2)] MISTAKEN FOR THE FRAGILE-X CHROMOSOME [(X) (Q27.3)] | 0 | 0 |
| 1933 | 0 | 0 | 735 1990 PRACTITIONER 234(1496):946-& BERNEY T FRAGILE-X SYNDROME | 0 | 0 |
| 1934 | 0 | 0 | 737 1990 PRENATAL DIAGNOSIS 10(8):546-546 WEBB TP RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 1935 | 0 | 0 | 747 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):35-35 TURNER G FRAGILE X-SYNDROME | 0 | 0 |
| 1936 | 0 | 1 | 748 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 SCHLESSINGER D; ZUCCHI I; NAGARAJA R; LITTLE RD; ABIDI F; et al. CLONING OF THE FRAGILE-X LOCUS IN THE CONTEXT OF YEAST ARTIFICIAL CHROMOSOME-BASED MAPPING OF XQ24-28 | 0 | 0 |
| 1937 | 0 | 0 | 749 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 POUSTKA A; DIETRICH A; KORN B; GROSS B; MONACO A; et al. MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION | 0 | 0 |
| 1938 | 0 | 0 | 750 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 KUHL D; PIERETTI M; REINER O; NELSON D FRAGILE-X SITE - MOLECULAR AND GENETIC-CHARACTERIZATION | 0 | 0 |
| 1939 | 0 | 0 | 751 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):76-76 OBERLE I; ROUSSEAU F; HEITZ D; DEVYS D; ZENGERLING S; et al. MOLECULAR-BASIS OF THE FRAGILE-X SYNDROME AND DIAGNOSTIC APPLICATIONS | 0 | 0 |
| 1940 | 0 | 0 | 752 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):76-76 YU S; KREMER E; PRITCHARD M; LYNCH M; NANCARROW J; et al. THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1941 | 0 | 0 | 753 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):103-103 ROCCHI M; MORABITO E; DINATALE P IDURONATE SULFATASE ACTIVITY ON LYMPHOBLASTOID CELL-LINES FROM SUBJECTS AFFECTED BY FRAGILE-X SYNDROME | 0 | 0 |
| 1942 | 0 | 0 | 754 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):139-139 HAGERMAN RJ; BRUNSCHWIG A; MILLER L; BUTLER MG SELECTED STANDARDS FOR ANTHROPOMETRIC MEASUREMENTS IN FRAGILE X-SYNDROME | 0 | 0 |
| 1943 | 0 | 0 | 755 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):158-158 RAMZY MI; SALINAS CF ORODENTAL FINDINGS IN AN EGYPTIAN SAMPLE OF FRAGILE-X CASES | 0 | 0 |
| 1944 | 0 | 0 | 756 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):159-159 REISS A; FREUND L; AYLWARD E NEUROANATOMY OF THE FRAGILE X SYNDROME | 0 | 0 |
| 1945 | 0 | 0 | 757 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):163-163 SEEMANOVA E; GOETZ P; SVOBODOVA M; LESNY I INCESTUOUS MATINGS IN FAMILIES WITH FRAGILE (X) SYNDROME | 0 | 0 |
| 1946 | 0 | 0 | 758 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):194-194 KUHL DPA; WARREN ST; RIGGINS GJ; NELSON DL; CASKEY CT USE OF CA REPEAT MARKER DXS548 FOR PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME AND THE IDENTIFICATION OF NEW POSSIBLY POLYMORPHIC SITES IN THE FRAGILE-X REGION | 0 | 0 |
| 1947 | 0 | 0 | 759 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):211-211 BROWN WT; GOONEWARDENA P; RAY J; MIEZEJESKI C; KRAWCZUN M; et al. PRENATALLY DETECTED FRAGILE X FEMALES - COUNSELING ISSUES AND LONG-TERM FOLLOW-UPS | 0 | 0 |
| 1948 | 0 | 0 | 760 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):221-221 KAHKONEN M; VAISANEN ML; WINGVIST R; LEISTI J PRENATAL-DIAGNOSIS OF FRAGILE X SYNDROME | 0 | 0 |
| 1949 | 0 | 0 | 762 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):235-235 LI Q; XU DD; ZHOU LY FRAGILE X-FREQUENCY IN MENTALLY-RETARDED CHILDREN AND IN FETAL BLOOD BY CORDOCENTESIS | 0 | 0 |
| 1950 | 0 | 0 | 763 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):257-257 JACKSONCOOK J; PISERCHIO C; VIRGINIA J MOSAIC XY/XYY AND FRAGILE-X IN A 4-YEAR-OLD MALE BODURTHA | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1951 | 0 | 0 | 764 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):267-267 KARIMINEJAD MH; RAHIMI M; SHIRNESHAN K; VAEZI SA; KARIMINEJAD R FRAGILE-X (BELL,MARTIN) SYNDROME IN AN IRANIAN FAMILY WITH 8 AFFECTED MEMBERS | 0 | 0 |
| 1952 | 0 | 0 | 765 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):269-269 LOZZIO CB; MATTESON K; CACHEIRO NL CARRIER DETECTION OF FRAGILE-X USING TRIMETHOPRIM AND DNA LINKAGE ANALYSES | 0 | 0 |
| 1953 | 0 | 0 | 766 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):269-269 PAJARES IL; DELICADO A; DETORRES ML; MARTIN VL; CASTROVIEJO IP; et al. FRAGILE-X SYNDROME WITH EXTRAMICROCHROMOSOME | 0 | 0 |
| 1954 | 0 | 1 | 767 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):270-270 MURTHY SK; KAR B FRAGILE-X SYNDROME IN MENTALLY-RETARDED POPULATION OF WESTERN INDIA | 0 | 0 |
| 1955 | 0 | 0 | 768 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):273-273 RISCILE GR FRAGILE-X PATIENTS WITH ATYPICAL PHENOTYPES | 0 | 0 |
| 1956 | 0 | 0 | 769 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):280-280 ZASLAV AL; BROWN WT THE SIGNIFICANCE OF LOW-LEVEL FRAGILE X EXPRESSION | 0 | 0 |
| 1957 | 0 | 0 | 770 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):287-287 RAFI SK; SURANA RB; ANDERSON LH; CHRISTOPHER KL; WILSON B; et al. HYPEROXIA ENHANCES THE INDUCTION OF FRAGILE-X SITE OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1958 | 0 | 0 | 771 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):289-289 BUCKLEY D; JALAL S; DEWALD G FRAGILE-X STUDIES - WHAT IS PRACTICAL | 0 | 0 |
| 1959 | 0 | 0 | 772 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):290-290 JENKINS E; GENOVESE M; DUNCAN C; GU H; SCHWARTZRICHSTEIN C; et al. COMMON FRAGILE SITE FRA(X)(Q27.2), PRESENT IN ONLY 1 OF 685 CASES SCREENED FOR THE FRAGILE-X SYNDROME | 0 | 0 |
| 1960 | 0 | 0 | 773 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):290-290 HOWARDPEEBLES PN FRAGILE-X TESTING OF FAMILY MEMBERS IN THE CLINICAL CYTOGENETICS LABORATORY - PERIMETERS AND PITFALLS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1961 | 0 | 0 | 774 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):291-291 LOGHINGROSSO NS; LAUANDOS JE; ALI VRA; GRACA CHN; SCHMIDT BJ SEARCHING FOR FRAGILE-X IN AN INSTITUTION FOR MENTALLY-HANDICAPPED IN BRAZIL | 0 | 0 |
| 1962 | 0 | 0 | 775 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):292-292 SHAPIRO LR; PETRELLA R; EALLONARDO SJ; WILMOT PL RELIABILITY OF OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION AS AN INDICATION OF SUCCESSFUL INDUCTION OF THE FRAGILE-X CHROMOSOME | 0 | 0 |
| 1963 | 0 | 0 | 776 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):293-293 TENGSTROM C; AUTIO S CHROMOSOMAL-ABERRATIONS IN 542 MENTALLY-RETARDED PATIENTS EXAMINED BY HIGH-RESOLUTION BANDING INCLUDING FRAGILE X-SCREENING | 0 | 0 |
| 1964 | 0 | 0 | 777 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):303-303 MCCOMBS J; ROUSE B; LOCKHART L; HOWARDPEEBLES P PRENATAL IDENTIFICATION OF FRAGILE-X AND A MARKER CHROMOSOME | 0 | 0 |
| 1965 | 0 | 0 | 778 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):331-331 TURNER G; ROBINSON H; LAING S; SHERMAN S SCREENING FOR THE FRAGILE X-SYNDROME - IMPACT OF GENETIC-COUNSELING ON REPRODUCTIVE CHOICES OF WOMEN AT RISK FOR HAVING AN AFFECTED CHILD | 0 | 0 |
| 1966 | 0 | 0 | 779 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):338-338 GLASS IA; DELMASTRO RG; LANYON WG; RAEBURN JA; KILPATRICK MW; et al. IDENTIFICATION OF DIAGNOSTIC DNA MARKERS FOR THE FRAGILE-X SYNDROME | 0 | 0 |
| 1967 | 0 | 0 | 780 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):341-341 GOONEWARDENA P; GLICKSMAN A; BROWN WT LINKAGE ANALYSIS OF PROXIMAL DNA MARKERS RN1 AND VK23 USED IN THE DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| 1968 | 0 | 0 | 781 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):353-353 NORDSTROM AM; VONKOSKULL H LINKAGE TO DXS52 IN A FRAGILE-X NEGATIVE FAMILY | 0 | 0 |
| 1969 | 0 | 0 | 782 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):357-357 RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; et al. A FREQUENT DINUCLEOTIDE POLYMORPHISM OF THE FRAGILE-X BREAKPOINT CLUSTER REGION IS TIGHTLY LINKED TO THE FRAGILE-X SYNDROME LOCUS | 0 | 0 |
| 1970 | 0 | 0 | 783 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):383-383 LEE JT; MURGIA A; WARREN S; NELSON D; NUSSBAUM R CONSTRUCTION OF A 600-KB YAC CONTIG PROXIMAL TO THE FRAGILE X-SITE | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1971 | 0 | 0 | 784 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):417-417 REINER O; VERKERK AJMH; PIERETTI M; PIZZUTI A; BLONDE L; et al. CHARACTERIZATION OF EXPRESSED SEQUENCES AT THE FRAGILE-X LOCUS | 0 | 0 |
| 1972 | 0 | 0 | 785 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):469-469 FISCH GS; SHAPIRO LR; SIMENSEN R; SCHWARTZ CE; FRYNS JP; et al. DIFFERENCES IN DECLINE IN IQ AMONG FRAGILE-X MALES - EVIDENCE FOR GENETIC-HETEROGENEITY | 0 | 0 |
| 1973 | 0 | 0 | 786 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):474-474 LOESCH DZ; HUGGINS R ESTIMATION OF THE EFFECTS OF FRAGILE-X ON DISTRIBUTIONS OF PHYSICAL AND INTELLECTUAL MEASURES USING A MAXIMUM-LIKELIHOOD SCORING TECHNIQUE | 0 | 0 |
| 1974 | 9 | 14 | 799 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):319-321 DAHL N; MALMGREN H; PETTERSSON U; HOLMGREN G; SEEMANOVA E; et al. CARRIER DETECTION OF THE FRAGILE-X SYNDROME USING FLANKING LOCI DXS98, DXS105, AND DXS304 | 0 | 0 |
| 1975 | 4 | 4 | 803 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):347-348 ROMANO V; MASCALI G; CHIAVETTA V; RAGUSA RM; BARLETTA C; et al. RFLP ANALYSIS IN 5 SICILIAN FAMILIES WITH THE FRAGILE-X SYNDROME | 0 | 0 |
| 1976 | 12 | 18 | 806 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):367-369 PELLISSIER MC; VOELCKEL MA; PIQUET C; MATTEI MG; MATTEI JF TRANSMISSION OF MENTAL-RETARDATION WITH FRAGILE-X SITE BY 2 NORMAL TRANSMITTER BROTHERS | 0 | 0 |
| 1977 | 4 | 15 | 810 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):380-383 PERGOLIZZI R; BROWN WT; GOONEWARDENA P; BHAN R; DOBKIN C; et al. MOLECULAR CHARACTERIZATION OF A DNA PROBE, U6.2, LOCATED CLOSE TO THE FRAGILE-X LOCUS | 0 | 0 |
| 1978 | 2 | 4 | 835 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(4):523-523 DREESEN JCFM; SMITS A; BRUNNER H RISK CALCULATIONS IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1979 | 2 | 5 | 836 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 |
| 1980 | 0 | 0 | 841 1991 ANNALS OF NEUROLOGY 30(3):450-450 BERRYKRAVIS E; HODGES C DEMONSTRATION OF ABNORMAL CYCLIC ADENOSINE-MONOPHOSPHATE PRODUCTION IN MULTIPLE TISSUES FROM INDIVIDUALS WITH FRAGILE X-SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1981 | 1 | 2 | 844 1991 BRITISH MEDICAL JOURNAL 302(6789):1359-1359 CHARATAN F GENE FOR FRAGILE-X SYNDROME DISCOVERED | 0 | 0 |
| 1982 | 0 | 0 | 852 1991 CLINICAL RESEARCH 39(3):A722-A722 BERRYKRAVIS E; HODGES C DEFECTIVE CYCLIC-AMP PRODUCTION IN TISSUES FROM PATIENTS WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1983 | 0 | 2 | 854 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 HOWARDPEEBLES PN FRAGILE X SCREENING VS FAMILY STUDIES (ESPECIALLY IN FEMALES) - LABORATORY PROCEDURES GUIDELINES | 0 | 0 |
| 1984 | 0 | 0 | 857 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2062-2062 DJABALI M; NGUYEN C; BIUNNO I; IKEDA JE; OOSTRA BA; et al. LASER MICRODISSECTION OF THE FRAGILE-X REGION ALLOWS ISOLATION OF COSMID CLONES CONTAINING CONSERVED SEQUENCES | 0 | 0 |
| 1985 | 0 | 2 | 858 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2062-2062 DIETRICH A; LANGENSTEIN G; TONIOLO D; WARREN ST; LEHRACH H; et al. A PHYSICAL MAP OF THE HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION | 0 | 0 |
| 1986 | 2 | 5 | 859 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2065-2065 GRAHAM CA; GRIER DG; CLARKSON M; STEWART FJ; NEVIN NC LINKAGE ANALYSIS IN FRAGILE-X SYNDROME | 0 | 0 |
| 1987 | 2 | 5 | 860 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2067-2067 HIRST M; NAKAHORI Y; KNIGHT S; ROCHE A; RAUT C; et al. A YAC CONTIG ACROSS THE FRAGILE-X REGION DERIVED FROM CHROMOSOME MICRODISSECTION MARKERS | 0 | 0 |
| 1988 | 0 | 0 | 861 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2076-2076 LYNCH M; KREMER EJ; PRITCHARD MA; YU S; BAKER E; et al. THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 0 | 0 |
| 1989 | 0 | 4 | 862 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2082-2082 POUSTKA A; DIETRICH A; KIOSCHIS P; KORN B; GROSS B; et al. MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION | 0 | 0 |
| 1990 | 2 | 8 | 882 1991 JOURNAL OF REPRODUCTION AND FERTILITY 91(1):203-206 TEWARI R; RAO SRV REPLICATION STATUS OF THE FRAGILE X-CHROMOSOME AND ITS IMPLICATIONS FOR REPRODUCTIVE-PERFORMANCE IN THE INDIAN MOLE RAT (NESOKIA-INDICA) | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1991 | 0 | 0 | 887 1991 M S-MEDECINE SCIENCES 7(4):378-379 OBERLE I; MANDEL JL FRAGILE-X MENTAL-RETARDATION - VERY LOCALIZED GENOMIC IMPRINTING CLOSELY LINKED TO CLINICAL EXPRESSION | 0 | 0 |
| 1992 | 0 | 0 | 888 1991 M S-MEDECINE SCIENCES 7(6):637-639 ROUSSEAU F; HEITZ D; OBERLE I; MANDEL JL; KRETZ C THE FRAGILE X-SYNDROME - NEW SURPRISES | 0 | 0 |
| 1993 | 0 | 0 | 899 1991 PEDIATRIC RESEARCH 29(4):A134-A134 SHAPIRO LR; EALLONARDO SJ; WILMOT PL OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION AND THE FRAGILE-X SYNDROME | 0 | 0 |
| 1994 | 3 | 4 | 908 1991 SCIENCE 253(5027):1467-1467 HECHT F FRAGILE-X GENE | 0 | 0 |
| 1995 | 2 | 5 | 932 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):161-161 HOWARDPEEBLES PN EFFECT OF DIALYZED SERA ON FRAGILE-X EXPRESSION | 0 | 0 |
| 1996 | 7 | 9 | 934 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):167-169 SHAPIRO LR; WILMOT PL; ANDREE LE PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X CHROMOSOME - FEASIBILITY AND SPEED OF INSITU CLONAL METHOD IN AMNIOTIC-FLUID CELL TISSUE-CULTURE | 0 | 0 |
| 1997 | 17 | 38 | 960 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(6):1050-1056 GLASS IA; DELMASTRO RG; LANYON WG; RAEBURN JA; KILPATRICK MW; et al. TIGHTLY LINKED POLYMORPHIC MARKERS FOR FRAGILE X-SYNDROME AND PRENATAL CYTOGENETIC DIAGNOSTIC EXPERIENCE | 0 | 0 |
| 1998 | 25 | 37 | 968 1992 ANNALS OF MEDICINE 24(6):453-456 POUSTKA A FRAGILE-X SYNDROME - MOLECULAR ANALYSIS REVEALS A NEW MECHANISM OF MUTATION IN HUMAN GENETIC-DISEASES | 0 | 0 |
| 1999 | 1 | 1 | 972 1992 ARCHIVES OF DISEASE IN CHILDHOOD 67(11):1337-1337 [Anon] SISTERS OF FRAGILE-X BOYS | 0 | 0 |
| 2000 | 10 | 13 | 979 1992 COMPTES RENDUS DES SEANCES DE LA SOCIETE DE BIOLOGIE ET DE SES FILIALES 186(4):363-370 BELDJORD C; RICHARD L FRAGILE-X SYNDROME - AN HERITABLE UNSTABLE ELEMENT | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2001 | 0 | 0 | 980 1992 CYTOGENETICS AND CELL GENETICS 60(3-4):265-265 SHAPIRO LR; WILMOT PL; ANDREE LE PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X CHROMOSOME - FEASIBILITY AND SPEED OF INSITU CLONAL METHOD IN AMNIOTIC-FLUID CELL TISSUE-CULTURE | 0 | 0 |
| 2002 | 0 | 0 | 981 1992 CYTOGENETICS AND CELL GENETICS 60(3-4):266-266 JACKY PB; JENKINS EC FRAGILE-X CYTOGENETIC GUIDELINES REVIEWED - RELEVANCE TO FRA(X) MOLECULAR GENETIC-STUDIES AND TO APPROPRIATENESS OF CHROMOSOME-STUDIES IN ALL CASES OF DEVELOPMENTAL DELAY - A DISCUSSION | 0 | 0 |
| 2003 | 1 | 1 | 985 1992 EUROPEAN JOURNAL OF PEDIATRICS 151(6):469-470 MUNDLOS S FRAGILE-X SOLVED | 0 | 0 |
| 2004 | 1 | 1 | 986 1992 EUROPEAN JOURNAL OF PEDIATRICS 151(8):617-617 MUNDLOS S GIRLS WITH THE FRAGILE-X SYNDROME | 0 | 0 |
| 2005 | 0 | 0 | 992 1992 INTERNATIONAL JOURNAL OF PSYCHOLOGY 27(3-4):327-327 FISCH GS; SHAPIRO LR; SIMENSEN RJ; FRYNS JP; BORGHGRAEF M; et al. LONGITUDINAL CHANGES IN IQ AMONG FRAGILE(X) MALES - CLINICAL-EVIDENCE FOR MORE THAN ONE MUTATION | 0 | 0 |
| 2006 | 0 | 0 | 993 1992 INTERNATIONAL JOURNAL OF PSYCHOLOGY 27(3-4):395-395 SIMENSEN RJ; SAUL RA; TARLETON JD; PHELAN MC NEUROPSYCHOLOGICAL FUNCTIONING IN FRAGILE X-SYNDROME AND MONOSOMY-X MOSAICISM - A CASE PRESENTATION | 0 | 0 |
| 2007 | 0 | 0 | 994 1992 INTERNATIONAL JOURNAL OF PSYCHOLOGY 27(3-4):397-398 FISCH GS; SHAPIRO LR; SIMENSEN RJ; FRYNS JP; BORGHGRAEF M; et al. LONGITUDINAL CHANGES IN IQ AMONG FRAGILE(X) MALES - CLINICAL-EVIDENCE FOR MORE THAN ONE MUTATION | 0 | 0 |
| 2008 | 16 | 34 | 998 1992 JOURNAL OF INHERITED METABOLIC DISEASE 15(4):532-538 HIRST MC; KNIGHT SM; NAKAHORI Y; ROCHE A; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 2009 | 0 | 0 | 1009 1992 M S-MEDECINE SCIENCES 8(3):252-254 GILGENKRANTZ H FRAGILE-X - WHATS NEW | 0 | 0 |
| 2010 | 0 | 0 | 1010 1992 M S-MEDECINE SCIENCES 8(8):878-878 DREYFUSS JC CLINICAL FRAGILE-X SYNDROME DUE TO TOTAL OR PARTIAL GENE DELETION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2011 | 8 | 19 | 1012 1992 MEDICINA CLINICA 98(4):131-133 PRIETO F; MARTINEZCASTELLANO F THE FRAGILE-X SYNDROME AND ITS RELATION WITH OTHER SYNDROMES LINKED TO CHROMOSOME-X ASSOCIATED WITH MENTAL-RETARDATION | 0 | 0 |
| 2012 | 0 | 0 | 1014 1992 MONATSSCHRIFT KINDERHEILKUNDE 140(7):404-404 KRUSE K GIRLS WITH FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) | 0 | 0 |
| 2013 | 0 | 0 | 1023 1992 PEDIATRIE 47(11):743-750 PELLISSIER MC; VOELCKEL MA; MATTEI JF FRAGILE-X SYNDROME - CURRENT KNOWLEDGE | 0 | 0 |
| 2014 | 0 | 0 | 1030 1993 AMERICAN FAMILY PHYSICIAN 47(5):1072-1073 SIMENSEN RJ FRAGILE-X SYNDROME | 0 | 0 |
| 2015 | 0 | 0 | 1038 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):31-31 HANSEN RS; CANFIELD TK; LAMB MM; GARTLER SM; LAIRD CD FRAGILE X-SYNDROME IS ASSOCIATED WITH A LARGE DOMAIN OF DELAYED REPLICATION AT THE FMR1 LOCUS | 0 | 0 |
| 2016 | 0 | 0 | 1039 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):40-40 SIOMI H; SIOMI MC; NUSSBAUM RL; DREYFUSS G THE PROTEIN PRODUCT OF THE FRAGILE X-GENE, FMR-1, HAS CHARACTERISTICS OF AN RNA-BINDING PROTEIN | 0 | 0 |
| 2017 | 0 | 0 | 1041 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):88-88 MADDALENA A; SPENCE WC; LEVINSON G; HOWARDPEEBLES PN FRAGILE-X PRENATAL-DIAGNOSIS IN KNOWN CARRIERS | 0 | 0 |
| 2018 | 0 | 0 | 1042 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):143-143 MAZZOCCO MMM; WHITE BN; HOLDEN JJA THE FRAGILE X SYNDROME - A FAMILY WITH 3 HOMOZYGOUS FRA(X) SISTERS | 0 | 0 |
| 2019 | 0 | 0 | 1044 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):182-182 KUNST C; KARICKHOFF L; ZERYLNICK C; HOLDEN J; NELSON DL; et al. IDENTIFICATION OF 2 POLYMORPHIC LOCI NEAR FMR-1 AND DEMONSTRATION OF MARKED LINKAGE DISEQUILIBRIUM WITHIN NORMAL AND BETWEEN ABNORMAL CGG-REPEAT LENGTHS | 0 | 0 |
| 2020 | 0 | 0 | 1045 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):432-432 FISCH GS; HOLDEN JJA; SIMENSEN R; CARPENTER NJ; HOWARDPEEBLES PN; et al. IS FRAGILE X-SYNDROME A PERVASIVE DEVELOPMENTAL DISABILITY - COGNITIVE AND ADAPTIVE ABILITIES IN MALES WITH THE FULL MUTATION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2021 | 0 | 0 | 1046 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):446-446 HINTON VJ; DOBKIN CS; BROWN WT; JENKINS EC; GOONEWARDENA P; et al. VARIABILITY OF VISUAL-SPATIAL DEFICITS OBSERVED IN FRAGILE X-FEMALES | 0 | 0 |
| 2022 | 0 | 0 | 1049 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):565-565 JENKINS EC; MORYS I; HENDERSON J; GENOVESE M; CARTER M; et al. THE EFFECT OF FRAGILE-X INDUCTION SYSTEMS ON CYTOGENETIC, PCR AND DIREDT DNA ANALYSES OF THE FMR-1 GENE IN CVS CULTURES | 0 | 0 |
| 2023 | 0 | 0 | 1052 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):744-744 ZHONG N; DOBKIN C; BROWN WT A 2ND HYPERMUTABLE DNA-SEQUENCE LOCATED WITHIN THE FRAGILE X-GENE | 0 | 0 |
| 2024 | 0 | 0 | 1053 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):781-781 BROWN WT; ZHONG N; YE L; DOBKIN C FOUNDER FRAGILE-X CHROMOSOMES | 0 | 0 |
| 2025 | 0 | 0 | 1054 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):828-828 MALMGREN H; GUSTAVSON KH; HOLMGREN G; PETTERSSON U; DAHL N STRONG FOUNDER EFFECT FOR THE FRAGILE X-SYNDROME IN SWEDEN | 0 | 0 |
| 2026 | 0 | 0 | 1055 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):850-850 RIGGINS GJ; SHERMAN SL; PHILLIPS CN; STOCK W; WESTBROOK CA; et al. A POLYMORPHIC CGG-REPEAT OF THE BCR GENE DEMONSTRATES A LACK OF IMPRINTING AND ALLELIC ASSOCIATION WITH PH1-POSITIVE LEUKEMIA | 0 | 0 |
| 2027 | 0 | 0 | 1056 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1126-1126 BERRYKRAVIS E; HICAR M CORRELATION OF CYCLIC-AMP PRODUCTION WITH LENGTH OF FMR-1 AMPLIFICATION MUTATION IN LYMPHOBLASTOID-CELLS (LCLS) FROM PATIENTS WITH FRAGILE-X SYNDROME (FRA-X) | 0 | 0 |
| 2028 | 0 | 0 | 1057 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1132-1132 BROWN CA; TESHIMA IE; CHITAYAT D; RAY PN IDENTIFICATION OF FULL MUTATION FRAGILE-X CARRIERS BY MULTIPLEX PCR OF THE REPEAT SEQUENCES IN THE FMR-1 AND ANDROGEN RECEPTOR GENES | 0 | 0 |
| 2029 | 0 | 0 | 1058 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1136-1136 CASTELLVIBEL S; KRUYER H; BANCHS I; MILA M; ESTIVILL X NONRADIOACTIVE PCR OF THE CGG REPEAT OF THE FRAGILE-X GENE | 0 | 0 |
| 2030 | 0 | 0 | 1059 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1206-1206 MUELLER OT; HARTSFIELD JK; GALLARDO LA; KOUSSEFF BG FRAGILE X-SYNDROME - DISCORDANT EXPRESSION OF FMR-1 WITH IDENTICAL SMALL CGG INSERTS IN 2 BROTHERS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2031 | 0 | 0 | 1061 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1222-1222 ROUSSEAU F; ROBB L; DERKALOUSTIAN V A MENTALLY NORMAL-MALE CARRIER OF A FRAGILE-X FULL MUTATION GAVE BIRTH TO A PREMUTATED DAUGHTER | 0 | 0 |
| 2032 | 0 | 0 | 1062 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1237-1237 TAYLOR AK; SAFANDA JF; FALL MZ; QUINCE C; LANG KA; et al. MOLECULAR PREDICTORS OF INVOLVEMENT IN FRAGILE-X FEMALES | 0 | 0 |
| 2033 | 0 | 0 | 1064 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1245-1245 VANDERHOUT AH; VANDERVLIES P; TUERLINGS J; SIKKENS E; OOSTRA BA; et al. A NORMAL TRANSMITTING MALE SHOWS A MOSAIC FMR1-PATTERN WITH CGG-REPEAT INSERTIONS OF 450-950 BASEPAIRS AND AN UNMETHYLATED CPG ISLAND | 0 | 0 |
| 2034 | 0 | 0 | 1065 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1435-1435 MALTER HE; KARICKHOFF L; TUCKER M; WIKER S; WRIGHT G; et al. SINGLE-CELL ANALYSIS OF THE REPEAT EXPANSION MUTATION ASSOCIATED WITH FRAGILE X-SYNDROME | 0 | 0 |
| 2035 | 0 | 0 | 1066 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1502-1502 RAVIA Y; PESSO R; BRAIERGOLDSTEIN O; BRAND N; BARKAI G; et al. SCREENING FOR FRAGILE-X MUTATION IN MENTALLY-RETARDED INDIVIDUALS | 0 | 0 |
| 2036 | 0 | 0 | 1067 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 |
| 2037 | 0 | 0 | 1068 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1738-1738 MERYASH D; MILLAN CA; PERGOLIZZI RG AN INDIVIDUAL WITH APPARENT X-LINKED MR AND MOSAICISM OF THE CGG REPEAT REGION IN THE FMR-1 GENE | 0 | 0 |
| 2038 | 0 | 0 | 1069 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1757-1757 SCHORDERET DF; PILLET N; PESCIA G; THONNEY F A COMPOUND HETEROZYGOTE FEMALE DETECTED IN A FAMILY WITH FRAGILE-X SYNDROME | 0 | 0 |
| 2039 | 0 | 0 | 1070 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1765-1765 YANAMANDRA K; RAO N; PETTENATI MJ; THOMAS IT UNEXPLAINED FRAGILE X-SYNDROME DNA TEST-RESULTS | 0 | 0 |
| 2040 | 2 | 3 | 1081 1993 AMERICAN JOURNAL ON MENTAL RETARDATION 97(4):477-479 SIMENSEN RJ FRAGILE X-SYNDROME - DIAGNOSIS, TREATMENT, AND RESEARCH - HAGERMAN,RJ, SILVERMAN,AC | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2041 | 0 | 0 | 1084 1993 BEHAVIOR GENETICS 23(6):555-555 HUGGINS RM THE USE OF ROBUST STATISTICAL-METHODS TO DETERMINE THE EFFECT OF GENOTYPE ON PHENOTYPE IN FRAGILE-X | 0 | 0 |
| 2042 | 0 | 0 | 1085 1993 BEHAVIOR GENETICS 23(6):557-557 LOESCH DZ; HUGGINS R; HAY DA; GODEON; AK; et al. GENOTYPE-PHENOTYPE RELATIONSHIPS IN FRAGILE-X - A FAMILY STUDY | 0 | 0 |
| 2043 | 0 | 0 | 1086 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 |
| 2044 | 0 | 0 | 1088 1993 BIOLOGICAL PSYCHIATRY 33(6A):A161-A161 ABRAMS M; FREUND L; REISS AL MOLECULAR PREDICTORS OF COGNITIVE FUNCTION IN FRAGILE X-SYNDROME | 0 | 0 |
| 2045 | 0 | 0 | 1099 1993 CYTOGENETICS AND CELL GENETICS 63(4):252-252 LUTHARDT F; SKOGERBOE K; SHADOAN P; DINNO N IDENTIFICATION OF DE-NOVO DEL(Y)(Q11.23) IN A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE USING A Y-CHROMOSOME COCKTAIL PROBE (DYZ1, DYZ3) | 0 | 0 |
| 2046 | 0 | 0 | 1100 1993 CYTOGENETICS AND CELL GENETICS 63(4):254-254 OSTROWSKI RS; GRASS FS; LOVETTJELLEMA J AN INVESTIGATION OF THE FRAGILE-X SITE AS IT RELATES TO CHROMOSOME OVERLAP IN CULTURED HUMAN WHITE BLOOD-CELLS | 0 | 0 |
| 2047 | 0 | 0 | 1101 1993 CYTOGENETICS AND CELL GENETICS 63(4):256-256 JACKY PB; BERRY TL; LAMB OA; LANGLOIS MI; OLSON CL; et al. ARE FRAGILE-X CHROMOSOME-STUDIES DEAD | 0 | 0 |
| 2048 | 1 | 1 | 1102 1993 CYTOGENETICS AND CELL GENETICS 64(3-4):187-187 SCHMIDT M X-CHROMOSOME INACTIVATION PATTERN IN INTERSTITIAL DELETIONS OF THE FRAGILE X-REGION | 0 | 0 |
| 2049 | 0 | 0 | 1121 1993 IRISH MEDICAL JOURNAL 86(5):172-172 LYNCH SA FRAGILE-X SYNDROME | 0 | 0 |
| 2050 | 0 | 0 | 1126 1993 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 14(4):282-282 HULL CE; HAGERMAN RJ A STUDY OF THE PHENOTYPE IN HETEROZYGOUS FRAGILE-X FEMALES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2051 | 1 | 1 | 1128 1993 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 37:111-111 COOPER M GAZE AVOIDING AND TORSO TURNING IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 2052 | 0 | 0 | 1130 1993 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 37:201-202 RAEBURN S PIECING TOGETHER THE FRAGILE-X - FRAGILE-X WORKSHOP, ROYAL-SOCIETY-OF-MEDICINE, LONDON, ENGLAND, 1 JULY 1992 | 0 | 0 |
| 2053 | 3 | 4 | 1145 1993 LANCET 342(8886-7):1563-1564 MOORE DY DIAGNOSING FRAGILE X-SYNDROME | 0 | 0 |
| 2054 | 4 | 13 | 1159 1993 NERVENHEILKUNDE 12(2):84-86 FROSTER UG CLINICAL AND MOLECULAR ASPECTS OF THE FRAGILE-X FORM OF MENTAL-RETARDATION (MARTIN-BELL SYNDROME) | 0 | 0 |
| 2055 | 0 | 6 | 1163 1993 PISMA V ZHURNAL TEKHNICHESKOI FIZIKI 19(14):43-48 KHAN VP; FEDOTOVA IV REPRESENTATION OF CGG (CHALCOGENIDE GLASSES) AS INORGANIC POLYMER AND POTENTIALITIES OF COMPUTATION OF EXCESSIVE HOMOBONDS FORMING IN THEM | 0 | 0 |
| 2056 | 2 | 10 | 1165 1993 SCIENTIST 7(19):16-16 CASKEY CT HOT PAPERS - MOLECULAR-GENETICS - VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX BY FU,Y.H., KUHL,D.P.A., PIZZUTI,A., ET-AL, AND AN UNSTABLE TRIPLET REPEAT IN A GENE-RELATED TO MYOTONIC MUSCULAR-DYSTROPHY BY FU,Y.H., PIZZUTI,A., FENWICK,R.G., ET-AL | 0 | 0 |
| 2057 | 0 | 0 | 1214 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):606-614 [Anon] ABSTRACTS FOR THE 6TH INTERNATIONAL WORKSHOP ON FRAGILE-X-SYNDROME AND X-LINKED MENTAL-RETARDATION | 0 | 0 |
| 2058 | 0 | 0 | 1222 1994 ANNALS OF NEUROLOGY 36(3):544-544 GUERREIRO M; MOURARIBEIRO MV; KATO M; CAMARGO E; DEFARIA APM BRAIN SINGLE-PHOTON EMISSION COMPUTED-TOMOGRAPHY IMAGING IN FRAGILE-X SYNDROME | 0 | 0 |
| 2059 | 5 | 30 | 1235 1994 GENETIC COUNSELING 5(2):129-139 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H PERSONAL INDEPENDENCE OF ADULT MENTALLY-RETARDED MEN WITH FRAGILE-X SYNDROME | 0 | 0 |
| 2060 | 4 | 6 | 1236 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2061 | 20 | 24 | 1253 1994 JAPANESE JOURNAL OF GENETICS 69(3):259-267 SEKI N; ISHIKIRIYAMA S; YAMAUCHI M; HORI T CYTOGENETIC AND MOLECULAR ANALYSIS OF DYNAMIC MUTATION ASSOCIATED WITH FRAGILE-X SYNDROME | 0 | 0 |
| 2062 | 0 | 0 | 1255 1994 JOURNAL OF CELLULAR BIOCHEMISTRY :184-184 WARREN ST OVERVIEW AND UPDATE ON FMR1 AND FRAGILE-X SYNDROME | 0 | 0 |
| 2063 | 0 | 0 | 1259 1994 JOURNAL OF MEDICAL GENETICS 31(2):170-170 STRAIN L; PORTEOUS MEM; BONTHRON DT PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION | 0 | 0 |
| 2064 | 0 | 0 | 1260 1994 JOURNAL OF MEDICAL GENETICS 31(2):173-173 WANG Q; GREEN EP; MATHEW CG; BOBROW M NONRADIOACTIVE PCR BASED SCREENING FOR FRAGILE-X SYNDROME | 0 | 0 |
| 2065 | 0 | 0 | 1261 1994 JOURNAL OF MEDICAL GENETICS 31(2):173-173 BULLOCK S; LINDLEY V COMPLEMENTARY CYTOGENETIC AND MOLECULAR ANALYSIS OF A REFERRAL FOR FRAGILE-X TESTING | 0 | 0 |
| 2066 | 1 | 6 | 1269 1994 KLINISCHE PADIATRIE 206(5):410-411 FEHLOW P; MIOSGE W; WALTHER F ASSOCIATION OF SAETHRE-CHOTZEN-SYNDROME AND FRAGILE-X-SYNDROME | 0 | 0 |
| 2067 | 8 | 10 | 1273 1994 MOLECULAR AND CELLULAR PROBES 8(3):241-244 DAVIDOW LS; BARBERIO D; CAO J; MCCORMICK I AN IMPROVED FRAGILE-X SOUTHERN BLOT PROBE WITHOUT THE CGGS ELIMINATES BACKGROUND BANDS | 0 | 0 |
| 2068 | 0 | 0 | 1275 1994 NEUROLOGY 44(4):A400-A400 GUERREIRO M; MOURARIBEIRO MVL; CAMARGO EE; KATO M; MENEZES JR; et al. NEUROBIOLOGY OF FRAGILE-X-SYNDROME (FXS) | 0 | 0 |
| 2069 | 0 | 0 | 1284 1995 AMERICAN JOURNAL OF EPIDEMIOLOGY 141(11):S50-S50 DAWSON DV; LACHIEWICZ AM BEHAVIORAL EPIDEMIOLOGY OF FRAGILE-X SYNDROME IN FEMALE PEDIATRIC POPULATIONS | 0 | 0 |
| 2070 | 0 | 0 | 1289 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):40-40 FENG Y; EBERHART DE; WARREN ST THE PROTEIN ABSENT IN FRAGILE-X SYNDROME (FMRP) IS A RIBOSOME-ASSOCIATED PROTEIN | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2071 | 0 | 0 | 1290 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):135-135 STALEYGANE L; FLYNN L; CRONISTERSILVERMAN A; HAGERMAN RJ EXPANDING THE ROLE OF THE GENETIC COUNSELOR WORKING WITH FRAGILE-X FAMILIES | 0 | 0 |
| 2072 | 0 | 0 | 1291 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):152-152 HUGHES MR; HADDAD BR; SUBRAMANIAN S; NASONKIN I; COTA J; et al. SINGLE-CELL DETECTION OF THE FMR1, HD, AND SCA1 TRINUCLEOTIDE REPEATS - APPLICATION TO PREIMPLANTATION DIAGNOSIS AND INSTABILITY ANALYSIS OF FRAGILE-X SYNDROME, HUNTINGTON DISEASE, AND SPINO-CEREBELLAR ATAXIA TYPE-1 | 0 | 0 |
| 2073 | 0 | 0 | 1293 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):196-196 EBERHART DE; FENG Y; WARREN ST IDENTIFICATION OF A CYTOPLASMIC ANCHOR DOMAIN RESPONSIBLE FOR THE SUBCELLULAR-LOCALIZATION OF THE FRAGILE-X MENTAL-RETARDATION PROTEIN, FMRP | 0 | 0 |
| 2074 | 0 | 0 | 1294 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):211-211 NELSON DL; KUNST CB; LUGENBEEL KA; RYDER OA; WARREN ST; et al. EVOLUTION OF THE CRYPTIC FMR1 CGG REPEAT | 0 | 0 |
| 2075 | 0 | 0 | 1295 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):494-494 GIANGRECO CA; STEELE MW; ASTON CE; CUMMINS JH; WENGER SL CLINICAL-CRITERIA FOR FRAGILE-X SOUTHERN BLOT DNA DIAGNOSTIC TESTING | 0 | 0 |
| 2076 | 0 | 0 | 1296 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):585-585 WRIGHTTALAMANTE C; CHEEMA A; RIDDLE JE; LUCKEY D; TAYLOR A; et al. A CONTROLLED-STUDY OF LONGITUDINAL IQ CHANGES IN FEMALES AND MALES WITH FRAGILE-X SYNDROME | 0 | 0 |
| 2077 | 0 | 0 | 1297 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):655-655 JENKINS EC; DOBKIN CS; DING X; LI SY; HOUCK GE; et al. THRESHOLD CGG REPEAT SIZE FOR FRAGILE SITE EXPRESSION WITHOUT METHYLATION IDENTIFIED IN LYMPHOCYTE, LYMPHOBLASTOID AND CLONAL LYMPHOBLASTOID CULTURES FROM AN FMR1 UNMETHYLATED MOSAIC FULL MUTATION INDIVIDUAL | 0 | 0 |
| 2078 | 0 | 0 | 1298 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):671-671 MARINI T; PFLUEGER S; NABER S; KARPELLS S; NAEEM R A 5-YEAR EXPERIENCE WITH FRAGILE-X TESTING | 0 | 0 |
| 2079 | 0 | 0 | 1299 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):692-692 RANCHINO B; TARAVATH A; KALICHMAN M; BURTON BB; MCCORQUODALE MM; et al. SELECTION AGAINST A MARKER CHROMOSOME IN FRAGILE-X-STRESSED CULTURES | 0 | 0 |
| 2080 | 0 | 0 | 1300 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):869-869 WINKELER KA; WARREN ST VARIATIONS IN THE LENGTH OF THE CGG-REPEAT OF FMR-1 AFFECT GENE-EXPRESSION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2081 | 1 | 1 | 1301 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):906-906 ASHLEY AE; MEADOWS KL; SHERMAN SL TRANSMISSION CHARACTERISTICS OF THE FMR-1 MUTATION IN THE COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 2082 | 0 | 0 | 1302 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):913-913 BROWN WT; ZHONG N; KAJANOJA E; SMITS B; CURLEY D; et al. FRAGILE-X FOUNDER CHROMOSOME EFFECTS AND NEW MUTATIONS | 0 | 0 |
| 2083 | 0 | 0 | 1303 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):919-919 CHIURAZZI P; KOZAK L; GENUARDI M; GIOVANNUCCIUZIELLI ML; BUSSANI C; et al. FRAGILE-X SYNDROME - ROUNDER CHROMOSOMES IN ITALY | 0 | 0 |
| 2084 | 0 | 0 | 1304 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):965-965 NOLIN SL; GLICKSMAN A; LEWIS FA; YE LL; HOUCK GE; et al. EVIDENCE FOR A FAMILIAL FACTOR INVOLVED IN CGG REPEAT EXPANSION IN FRAGILE-X SYNDROME | 0 | 0 |
| 2085 | 0 | 0 | 1305 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1088-1088 CURLEY D; ZHONG N; WANG DW; JU W; DOBKIN C; et al. NEW INTRAGENIC ALU POLYMORPHISMS IN THE FRAGILE-X GENE | 0 | 0 |
| 2086 | 0 | 0 | 1306 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1218-1218 FALIKBORENSTEIN TC; YALON M; SHACHAK L; DAR C; BOROCHOWITZ Z; et al. LONG UNINTERRUPTED CGG REPEATS WITHIN THE FMR1 GENE - POSSIBLE MECHANISM FOR THE PREVALENCE OF THE FRAGILE-X SYNDROME AMONG TUNISIAN JEWS | 0 | 0 |
| 2087 | 0 | 0 | 1307 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1273-1273 MILA M; CASTELLVIBEL S; BARCELO A; SANCHEZ A; JIMENEZ D; et al. MUTATIONS IN THE CPG ISLAND OF THE FMR1 GENE - ARE THEY RESPONSIBLE FOR FRAGILE-X SYNDROME | 0 | 0 |
| 2088 | 0 | 0 | 1308 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 |
| 2089 | 0 | 0 | 1309 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1344-1344 WILLEMSEN R; BAKKER C; MANDEL JL; DEVRIES B; DEVYS D; et al. RAPID SCREENING-TEST FOR FRAGILE-X SYNDROME | 0 | 0 |
| 2090 | 0 | 0 | 1310 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1359-1359 BAKKER C; DEGRAAFF E; ZHONG N; WILLEMSEN R; OOSTRA B INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF FMR1 PROTEIN IN A MALE-PATIENT WITH A LUNG-TUMOR | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2091 | 0 | 0 | 1312 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1407-1407 JOHNSON JP; CURRY C; MICEK M; LOUIE E; ABRAMS L; et al. TRANSMISSION OF STABLE AND UNSTABLE PREMUTATIONS FROM GREAT-GRANDMOTHER AND GREAT-GRANDFATHER RESPECTIVELY - LESSONS FOR GENETIC-COUNSELING IN FRAGILE-X SYNDROME FAMILIES | 0 | 0 |
| 2092 | 0 | 0 | 1313 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 |
| 2093 | 0 | 0 | 1314 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 |
| 2094 | 0 | 0 | 1315 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1705-1705 DEVRIES BBA; VANDENOUWELAND AMW; MOHKAMSING S; HALLEY DJJ; TIBBEN A; et al. ACCEPTANCE OF SCREENING FOR THE FRAGILE-X SYNDROME AMONG 1878 MENTALLY-RETARDED INDIVIDUALS IN INSTITUTES AND SPECIAL SCHOOLS IN THE NETHERLANDS | 0 | 0 |
| 2095 | 0 | 0 | 1316 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1838-1838 EIGEL A; ZYGULSKA M; DOLSCHEID T; BOGDANOVA N; DWORNICZAK B; et al. FRAGILE-X PREMUTATION FREQUENCY IN NORTHERN THAILAND | 0 | 0 |
| 2096 | 1 | 1 | 1317 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 |
| 2097 | 0 | 0 | 1318 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 |
| 2098 | 0 | 0 | 1319 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 |
| 2099 | 0 | 0 | 1320 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1947-1947 BROWN CA; BRASINGTON CK; GRASS FS PATERNAL TRANSMISSION OF A FULL MUTATION IN THE FMR1 GENE - IDENTIFICATION OF PATERNAL CGG REPEAT SHES IN MULTIPLE TISSUES | 0 | 0 |
| 2100 | 1 | 9 | 1329 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):526-526 SCHIANO CM; DEMB HB; BROWN WT LACK OF SIGNIFICANT ASSOCIATION BETWEEN SPINA-BIFIDA AND THE FRAGILE-X SYNDROME | 0 | 0 |