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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1801 | 1 | 6 | 874 1991 JOURNAL OF MEDICAL GENETICS 28(12):837-839 GRIFFITHS MJ; STRACHAN MC A SINGLE LYMPHOCYTE CULTURE FOR FRAGILE-X INDUCTION AND PROMETAPHASE CHROMOSOME ANALYSIS | 0 | 0 |
| 1802 | 2 | 8 | 875 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 |
| 1803 | 0 | 0 | 880 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 |
| 1804 | 0 | 0 | 881 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 |
| 1805 | 0 | 0 | 892 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 |
| 1806 | 3 | 4 | 900 1991 SCIENCE 253(5027):1467-1467 HECHT F FRAGILE-X GENE | 0 | 0 |
| 1807 | 2 | 5 | 924 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):161-161 HOWARDPEEBLES PN EFFECT OF DIALYZED SERA ON FRAGILE-X EXPRESSION | 0 | 0 |
| 1808 | 7 | 9 | 926 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 |
| 1809 | 17 | 38 | 951 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(6):1050-1056 GLASS IA; DELMASTRO RG; LANYON WG; RAEBURN JA; KILPATRICK MW; WEBB TP; CONNOR JM TIGHTLY LINKED POLYMORPHIC MARKERS FOR FRAGILE X-SYNDROME AND PRENATAL CYTOGENETIC DIAGNOSTIC EXPERIENCE | 0 | 0 |
| 1810 | 25 | 37 | 959 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1811 | 1 | 1 | 963 1992 ARCHIVES OF DISEASE IN CHILDHOOD 67(11):1337-1337 [Anon] SISTERS OF FRAGILE-X BOYS | 0 | 0 |
| 1812 | 10 | 13 | 970 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 |
| 1813 | 0 | 0 | 971 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 |
| 1814 | 0 | 0 | 972 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 |
| 1815 | 1 | 1 | 976 1992 EUROPEAN JOURNAL OF PEDIATRICS 151(6):469-470 MUNDLOS S FRAGILE-X SOLVED | 0 | 0 |
| 1816 | 1 | 1 | 977 1992 EUROPEAN JOURNAL OF PEDIATRICS 151(8):617-617 MUNDLOS S GIRLS WITH THE FRAGILE-X SYNDROME | 0 | 0 |
| 1817 | 0 | 0 | 983 1992 INTERNATIONAL JOURNAL OF PSYCHOLOGY 27(3-4):327-327 FISCH GS; SHAPIRO LR; SIMENSEN RJ; FRYNS JP; BORGHGRAEF M; CURFS LM; HOWARDPEEBLES PN; ARINAMI T; MAVROU A LONGITUDINAL CHANGES IN IQ AMONG FRAGILE(X) MALES - CLINICAL-EVIDENCE FOR MORE THAN ONE MUTATION | 0 | 0 |
| 1818 | 0 | 0 | 984 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 |
| 1819 | 0 | 0 | 985 1992 INTERNATIONAL JOURNAL OF PSYCHOLOGY 27(3-4):397-398 FISCH GS; SHAPIRO LR; SIMENSEN RJ; FRYNS JP; BORGHGRAEF M; CURFS LK; HOWARDPEEBLES PN; ARINAMI T; MAVROU A LONGITUDINAL CHANGES IN IQ AMONG FRAGILE(X) MALES - CLINICAL-EVIDENCE FOR MORE THAN ONE MUTATION | 0 | 0 |
| 1820 | 16 | 34 | 989 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1821 | 0 | 0 | 1000 1992 M S-MEDECINE SCIENCES 8(3):252-254 GILGENKRANTZ H FRAGILE-X - WHATS NEW | 0 | 0 |
| 1822 | 0 | 0 | 1001 1992 M S-MEDECINE SCIENCES 8(8):878-878 DREYFUSS JC CLINICAL FRAGILE-X SYNDROME DUE TO TOTAL OR PARTIAL GENE DELETION | 0 | 0 |
| 1823 | 8 | 19 | 1003 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 |
| 1824 | 0 | 0 | 1005 1992 MONATSSCHRIFT KINDERHEILKUNDE 140(7):404-404 KRUSE K GIRLS WITH FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) | 0 | 0 |
| 1825 | 0 | 0 | 1013 1992 PEDIATRIE 47(11):743-750 PELLISSIER MC; VOELCKEL MA; MATTEI JF FRAGILE-X SYNDROME - CURRENT KNOWLEDGE | 0 | 0 |
| 1826 | 0 | 0 | 1020 1993 AMERICAN FAMILY PHYSICIAN 47(5):1072-1073 SIMENSEN RJ FRAGILE-X SYNDROME | 0 | 0 |
| 1827 | 0 | 0 | 1028 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 |
| 1828 | 0 | 0 | 1029 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 |
| 1829 | 0 | 0 | 1031 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 |
| 1830 | 0 | 0 | 1032 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1831 | 0 | 0 | 1034 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):432-432 FISCH GS; HOLDEN JJA; SIMENSEN R; CARPENTER NJ; HOWARDPEEBLES PN; MADDALENA A; SANDGRUND A; JACQUES JR; MCGANN B IS FRAGILE X-SYNDROME A PERVASIVE DEVELOPMENTAL DISABILITY - COGNITIVE AND ADAPTIVE ABILITIES IN MALES WITH THE FULL MUTATION | 0 | 0 |
| 1832 | 0 | 0 | 1035 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):446-446 HINTON VJ; DOBKIN CS; BROWN WT; JENKINS EC; GOONEWARDENA P; MIEZEJESKI CM VARIABILITY OF VISUAL-SPATIAL DEFICITS OBSERVED IN FRAGILE X-FEMALES | 0 | 0 |
| 1833 | 0 | 0 | 1038 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):565-565 JENKINS EC; MORYS I; HENDERSON J; GENOVESE M; CARTER M; LI SY; HOUCK GA; DING XH; STARKHOUCK SL; DOBKIN CA; BROWN WT THE EFFECT OF FRAGILE-X INDUCTION SYSTEMS ON CYTOGENETIC, PCR AND DIREDT DNA ANALYSES OF THE FMR-1 GENE IN CVS CULTURES | 0 | 0 |
| 1834 | 0 | 0 | 1040 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 |
| 1835 | 0 | 0 | 1041 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):781-781 BROWN WT; ZHONG N; YE L; DOBKIN C FOUNDER FRAGILE-X CHROMOSOMES | 0 | 0 |
| 1836 | 0 | 0 | 1042 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 |
| 1837 | 0 | 0 | 1043 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 |
| 1838 | 0 | 0 | 1044 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 |
| 1839 | 0 | 0 | 1045 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 |
| 1840 | 0 | 0 | 1046 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 |
| 1841 | 0 | 0 | 1048 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 |
| 1842 | 0 | 0 | 1049 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1237-1237 TAYLOR AK; SAFANDA JF; FALL MZ; QUINCE C; LANG KA; HULL CE; CARPENTER I; STALEY LW; HAGERMAN RJ MOLECULAR PREDICTORS OF INVOLVEMENT IN FRAGILE-X FEMALES | 0 | 0 |
| 1843 | 0 | 0 | 1051 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1435-1435 MALTER HE; KARICKHOFF L; TUCKER M; WIKER S; WRIGHT G; MORTON P; MASSEY JB; ELSNER C; WARREN ST SINGLE-CELL ANALYSIS OF THE REPEAT EXPANSION MUTATION ASSOCIATED WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1844 | 0 | 0 | 1052 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1502-1502 RAVIA Y; PESSO R; BRAIERGOLDSTEIN O; BRAND N; BARKAI G; GOLDMAN B SCREENING FOR FRAGILE-X MUTATION IN MENTALLY-RETARDED INDIVIDUALS | 0 | 0 |
| 1845 | 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 |
| 1846 | 0 | 0 | 1054 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 |
| 1847 | 0 | 0 | 1055 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 |
| 1848 | 2 | 3 | 1066 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 |
| 1849 | 0 | 0 | 1069 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 |
| 1850 | 0 | 0 | 1070 1993 BEHAVIOR GENETICS 23(6):557-557 LOESCH DZ; HUGGINS R; HAY DA; GODEON AK; MULLEY JC; SUTHERLAND GR GENOTYPE-PHENOTYPE RELATIONSHIPS IN FRAGILE-X - A FAMILY STUDY | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1851 | 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 |
| 1852 | 0 | 0 | 1073 1993 BIOLOGICAL PSYCHIATRY 33(6A):A161-A161 ABRAMS M; FREUND L; REISS AL MOLECULAR PREDICTORS OF COGNITIVE FUNCTION IN FRAGILE X-SYNDROME | 0 | 0 |
| 1853 | 0 | 0 | 1084 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 |
| 1854 | 0 | 0 | 1085 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 |
| 1855 | 0 | 0 | 1086 1993 CYTOGENETICS AND CELL GENETICS 63(4):256-256 JACKY PB; BERRY TL; LAMB OA; LANGLOIS MI; OLSON CL; REISS JA; WEEKS FF; YOSHITOMI MJ ARE FRAGILE-X CHROMOSOME-STUDIES DEAD | 0 | 0 |
| 1856 | 1 | 1 | 1087 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 |
| 1857 | 0 | 0 | 1104 1993 IRISH MEDICAL JOURNAL 86(5):172-172 LYNCH SA FRAGILE-X SYNDROME | 0 | 0 |
| 1858 | 0 | 0 | 1109 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 |
| 1859 | 1 | 1 | 1111 1993 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 37:111-111 COOPER M GAZE AVOIDING AND TORSO TURNING IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1860 | 0 | 0 | 1113 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1861 | 3 | 4 | 1128 1993 LANCET 342(8886-7):1563-1564 MOORE DY DIAGNOSING FRAGILE X-SYNDROME | 0 | 0 |
| 1862 | 4 | 13 | 1141 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 |
| 1863 | 2 | 10 | 1146 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 |
| 1864 | 0 | 0 | 1193 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 |
| 1865 | 0 | 0 | 1201 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 |
| 1866 | 5 | 30 | 1213 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 |
| 1867 | 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 |
| 1868 | 20 | 24 | 1229 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 |
| 1869 | 0 | 0 | 1231 1994 JOURNAL OF CELLULAR BIOCHEMISTRY :184-184 WARREN ST OVERVIEW AND UPDATE ON FMR1 AND FRAGILE-X SYNDROME | 0 | 0 |
| 1870 | 0 | 0 | 1235 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1871 | 0 | 0 | 1236 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 |
| 1872 | 0 | 0 | 1237 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 |
| 1873 | 1 | 6 | 1245 1994 KLINISCHE PADIATRIE 206(5):410-411 FEHLOW P; MIOSGE W; WALTHER F ASSOCIATION OF SAETHRE-CHOTZEN-SYNDROME AND FRAGILE-X-SYNDROME | 0 | 0 |
| 1874 | 8 | 10 | 1249 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 |
| 1875 | 0 | 0 | 1250 1994 NEUROLOGY 44(4):A400-A400 GUERREIRO M; MOURARIBEIRO MVL; CAMARGO EE; KATO M; MENEZES JR; GUERREIRO CAM NEUROBIOLOGY OF FRAGILE-X-SYNDROME (FXS) | 0 | 0 |
| 1876 | 0 | 0 | 1258 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 |
| 1877 | 0 | 0 | 1263 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 |
| 1878 | 0 | 0 | 1264 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 |
| 1879 | 0 | 0 | 1265 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):152-152 HUGHES MR; HADDAD BR; SUBRAMANIAN S; NASONKIN I; COTA J; CHONG SS 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 |
| 1880 | 0 | 0 | 1267 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1881 | 0 | 0 | 1268 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 |
| 1882 | 0 | 0 | 1269 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):585-585 WRIGHTTALAMANTE C; CHEEMA A; RIDDLE JE; LUCKEY D; TAYLOR A; HAGERMAN RJ A CONTROLLED-STUDY OF LONGITUDINAL IQ CHANGES IN FEMALES AND MALES WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1883 | 0 | 0 | 1270 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 |
| 1884 | 0 | 0 | 1271 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):692-692 RANCHINO B; TARAVATH A; KALICHMAN M; BURTON BB; MCCORQUODALE MM; MCCORQUODALE DJ SELECTION AGAINST A MARKER CHROMOSOME IN FRAGILE-X-STRESSED CULTURES | 0 | 0 |
| 1885 | 1 | 1 | 1272 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 |
| 1886 | 0 | 0 | 1273 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):913-913 BROWN WT; ZHONG N; KAJANOJA E; SMITS B; CURLEY D; WANG D; JU W; HOUCK G; NOLIN S; RYYNANEN M FRAGILE-X FOUNDER CHROMOSOME EFFECTS AND NEW MUTATIONS | 0 | 0 |
| 1887 | 0 | 0 | 1274 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):919-919 CHIURAZZI P; KOZAK L; GENUARDI M; GIOVANNUCCIUZIELLI ML; BUSSANI C; DAGNABRICARELLI F; GRASSO M; PERRONE L; SEBASTIO G; SPERANDEO MP; OOSTRA BA; NERI G FRAGILE-X SYNDROME - ROUNDER CHROMOSOMES IN ITALY | 0 | 0 |
| 1888 | 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 |
| 1889 | 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 |
| 1890 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1891 | 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 |
| 1892 | 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 |
| 1893 | 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 |
| 1894 | 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 |
| 1895 | 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 |
| 1896 | 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 |
| 1897 | 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 |
| 1898 | 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 |
| 1899 | 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 |
| 1900 | 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 |
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