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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by NCR.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1101 | 5 | 16 | 341 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):475-481 JENKINS EC; KASTIN BR; KRAWCZUN MS; LELE KP; SILVERMAN WP; BROWN WT FRAGILE-X CHROMOSOME FREQUENCY IS CONSISTENT TEMPORALLY AND WITHIN REPLICATE CULTURES | 2 | 3 |
| 1102 | 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 |
| 1103 | 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 |
| 1104 | 4 | 16 | 403 1986 NEUROPSYCHOLOGIA 24(3):405-409 MIEZEJESKI CM; JENKINS EC; HILL AL; WISNIEWSKI K; FRENCH JH; BROWN WT A PROFILE OF COGNITIVE DEFICIT IN FEMALES FROM FRAGILE-X FAMILIES | 47 | 60 |
| 1105 | 4 | 16 | 512 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):99-107 FILIPPI G; PECILE V; RINALDI A; SINISCALCO M FRAGILE-X MUTATION AND KLINEFELTER SYNDROME - A REAPPRAISAL | 9 | 13 |
| 1106 | 7 | 16 | 545 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):641-654 SCHWARTZ CE; PHELAN MC; PULLIAM LH; WILKES G; VANNER LV; ALBIEZ KL; POTTS WA; ROGERS RC; SCHROER RJ; SAUL RA; PROUTY LA; DEAN JH; TAYLOR HA; STEVENSON RE FRAGILE-X SYNDROME - INCIDENCE, CLINICAL AND CYTOGENETIC FINDINGS IN THE BLACK AND WHITE-POPULATIONS OF SOUTH-CAROLINA | 12 | 15 |
| 1107 | 7 | 16 | 643 1989 HUMAN GENETICS 82(3):216-218 DAHL N; HAMMARSTROMHEEROMA K; GOONEWARDENA P; WADELIUS C; GUSTAVSON KH; HOLMGREN G; VANOMMEN GJB; PETTERSSON U ISOLATION OF A DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 17 | 32 |
| 1108 | 10 | 16 | 649 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):417-421 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ THE FRAGILE-X MARKER AND AUTISM IN PERSPECTIVE | 19 | 37 |
| 1109 | 9 | 16 | 679 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 36(1):122-125 VANROY BC; WILLEMS PJ; VITS LJ; CEULEMANS BP; COUCKE PJ; VANDERAUWERA BJ; LORMANS JAG; DUMON JE 2 BROTHERS WITH MENTAL-RETARDATION DISCORDANT FOR THE FRAGILE-X SYNDROME | 3 | 4 |
| 1110 | 7 | 16 | 807 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):404-407 FISCH GS; SILVERMAN W; JENKINS EC GENETIC AND OTHER FACTORS THAT CONTRIBUTE TO VARIABILITY IN CYTOGENETIC EXPRESSION IN FRAGILE-X MALES | 4 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1111 | 4 | 16 | 810 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):418-420 LEDBETTER SA; SCHWARTZ CE; DAVIES KE; LEDBETTER DH NEW SOMATIC-CELL HYBRIDS FOR PHYSICAL MAPPING IN DISTAL XQ AND THE FRAGILE-X REGION | 0 | 14 |
| 1112 | 7 | 16 | 861 1991 HUMAN GENETICS 87(3):369-372 HULSEBOS TJM; OOSTRA BA; BROERSEN S; SMITS A; VANOOST BA; WESTERVELD A NEW DISTAL MARKER CLOSELY LINKED TO THE FRAGILE-X LOCUS | 4 | 13 |
| 1113 | 1 | 16 | 920 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):124-127 TIROSH E; BOROCHOWITZ Z SLEEP-APNEA IN FRAGILE-X SYNDROME | 3 | 5 |
| 1114 | 11 | 16 | 1006 1992 NATURE GENETICS 1(3):157-158 HAGERMAN R CLINICAL CONUNDRUMS IN FRAGILE-X SYNDROME | 7 | 8 |
| 1115 | 11 | 16 | 1102 1993 HUMAN MOLECULAR GENETICS 2(11):1973-1974 TARLETON J; RICHIE R; SCHWARTZ C; RAO K; AYLSWORTH AS; LACHIEWICZ A AN EXTENSIVE DE-NOVO DELETION REMOVING FMR1 IN A PATIENT WITH MENTAL-RETARDATION AND THE FRAGILE X-SYNDROME PHENOTYPE | 29 | 50 |
| 1116 | 9 | 16 | 1162 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):353-357 FISCH GS; SIMENSEN R; ARINAMI T; BORGHGRAEF M; FRYNS JP LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X FEMALES - A PRELIMINARY MULTICENTER ANALYSIS | 9 | 10 |
| 1117 | 12 | 16 | 1178 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):454-457 TROTTIER Y; IMBERT G; POUSTKA A; FRYNS JP; MANDEL JL MALE WITH TYPICAL FRAGILE-X PHENOTYPE IS DELETED FOR PART OF THE FMR1 GENE AND FOR ABOUT 100 KB OF UPSTREAM REGION | 15 | 27 |
| 1118 | 1 | 16 | 1205 1994 CANCER RESEARCH 54(19):5212-5216 LEE ST; MCGLENNEN RC; LITZ CE CLONAL DETERMINATION BY THE FRAGILE-X (FMR1) AND PHOSPHOGLYCERATE KINASE (PGK) GENES IN HEMATOLOGICAL MALIGNANCIES | 1 | 12 |
| 1119 | 13 | 16 | 1228 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):552-553 CASKEY CT FRAGILE-X SYNDROME - IMPROVING UNDERSTANDING AND DIAGNOSIS | 2 | 2 |
| 1120 | 3 | 16 | 1326 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):218-222 Musumeci SA; Ferri R; Elia M; DalGracco S; Scuderi C; Stefanini MC; Castano A; Azan G Sleep neurophysiology in fragile X patients | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1121 | 13 | 16 | 1345 1995 DIAGNOSTIC MOLECULAR PATHOLOGY 4(3):158-161 NABER SP MOLECULAR DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| 1122 | 12 | 16 | 1521 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):209-212 Fombonne E Epidemiological studies of fragile X syndrome | 0 | 0 |
| 1123 | 10 | 16 | 1582 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; Naeem R A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol | 1 | 2 |
| 1124 | 10 | 16 | 1592 1997 HUMAN GENETICS 101(2):186-189 Pesso R; Barkai G; Ravia Y; Gak E; Frydman M; Goldman B; Friedman E No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome | 2 | 3 |
| 1125 | 9 | 16 | 1888 2000 GENETIC TESTING 4(3):235-239 Tzountzouris J; Kennedy D; Skuterud M; Connolly-Wilson M; Holden JJA; Lin CC; Mak-Tam E; Somerville MJ; Summers AM; Allingham-Hawkins DJ Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome | 0 | 1 |
| 1126 | 8 | 16 | 1912 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:81-85 Sabaratnam M Pathological and neuropathological findings in two males with fragile-X syndrome | 2 | 4 |
| 1127 | 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 |
| 1128 | 8 | 16 | 2175 2002 NATURE MEDICINE 8(11):1204-1205 Hansen RS; Laird CD A new regulatory pathway for fragile X syndrome? | 0 | 0 |
| 1129 | 9 | 16 | 2314 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 124A(2):213-215 Marshall I; Betensky BP; Goseco A; Vogiatzi MV; Flieder D Fragile x and mosaic 45,X/46,XY mixed gonadal dysgenesis in a girl with ambiguous genitalia | 0 | 0 |
| 1130 | 10 | 16 | 2339 2004 JOURNAL OF MEDICAL GENETICS 41(4) Zhou Y; Law HY; Boehm CD; Yoon CS; Cutting GR; Ng ISL; Chong SS Robust fragile X (CGG)(n) genotype classification using a methylation specific triple PCR assay | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1131 | 1 | 15 | 34 1981 PEDIATRICS 68(4):594-595 GERALD PS X-LINKED MENTAL-RETARDATION AND THE FRAGILE-X SYNDROME | 5 | 11 |
| 1132 | 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 |
| 1133 | 2 | 15 | 112 1983 ANNALES DE GENETIQUE 26(3):171-173 JACKY PB; DILL FJ FRAGILE-X CHROMOSOME AND CHROMOSOME CONDENSATION | 1 | 4 |
| 1134 | 3 | 15 | 129 1983 CLINICAL GENETICS 24(6):393-398 BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G; NORDENSON I; PALSSONSTRAE U FRAGILE X-SYNDROME IN MILDLY MENTALLY-RETARDED CHILDREN IN A NORTHERN SWEDISH COUNTY - A PREVALENCE STUDY | 42 | 67 |
| 1135 | 5 | 15 | 165 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(3):284-286 MIXON JC; DEV VG UNDERSTANDING THE FRAGILE X-SYNDROME | 0 | 2 |
| 1136 | 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 |
| 1137 | 3 | 15 | 296 1985 JOURNAL OF MEDICAL GENETICS 22(2):85-91 TUCKERMAN E; WEBB T; BUNDEY SE FREQUENCY AND REPLICATION STATUS OF THE FRAGILE-X, FRA(X)(Q27-28), IN A PAIR OF MONOZYGOTIC TWINS OF MARKEDLY DIFFERING INTELLIGENCE | 21 | 36 |
| 1138 | 7 | 15 | 299 1985 JOURNAL OF NEUROGENETICS 2(3):231-237 FORSTERGIBSON CJ; MULLIGAN LM; PARTINGTON MW; SIMPSON NE; HOLDEN JJA; WHITE BN THE GENETIC-DISTANCE BETWEEN THE COAGULATION FACTOR-IX GENE AND THE LOCUS FOR THE FRAGILE-X SYNDROME - CLINICAL IMPLICATIONS | 13 | 23 |
| 1139 | 4 | 15 | 310 1985 SOMATIC CELL AND MOLECULAR GENETICS 11(4):353-357 WANG JCC; ERBE RW THYMIDYLATE METABOLISM IN FRAGILE-X SYNDROME CELLS | 3 | 5 |
| 1140 | 6 | 15 | 351 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):643-664 BROWN WT; GROSS AC; CHAN CB; JENKINS EC DNA LINKAGE STUDIES IN THE FRAGILE-X SYNDROME SUGGEST GENETIC-HETEROGENEITY | 36 | 49 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1141 | 3 | 15 | 385 1986 HUMAN GENETICS 73(1):20-22 ABRUZZO MA; PETTAY D; MAYER M; JACOBS PA THE EFFECT OF CAFFEINE ON FRAGILE-X EXPRESSION | 9 | 12 |
| 1142 | 0 | 15 | 450 1987 HUMAN GENETICS 75(1):4-6 AMAROSE AP; HUTTENLOCHER PR; SPRUDZS RM; LAITSCH TJ; PETTENATI MJ A HERITABLE FRAGILE 12Q24.13 SEGREGATING IN A FAMILY WITH THE FRAGILE X-CHROMOSOME | 2 | 14 |
| 1143 | 2 | 15 | 556 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):767-773 BUTLER MG; FLETCHER M; GALE DD; MEANEY FJ; MCLEOD DR; FAGAN J; CARPENTER NJ METACARPOPHALANGEAL PATTERN PROFILE ANALYSIS IN FRAGILE-X SYNDROME | 4 | 8 |
| 1144 | 4 | 15 | 803 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):380-383 PERGOLIZZI R; BROWN WT; GOONEWARDENA P; BHAN R; DOBKIN C; DAHL N; PETTERSSON U MOLECULAR CHARACTERIZATION OF A DNA PROBE, U6.2, LOCATED CLOSE TO THE FRAGILE-X LOCUS | 0 | 0 |
| 1145 | 7 | 15 | 822 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):503-504 CRONISTER A; HAGERMAN RJ; WITTENBERGER M; AMIRI K MENTAL IMPAIRMENT IN CYTOGENETICALLY POSITIVE FRAGILE-X FEMALES | 14 | 15 |
| 1146 | 5 | 15 | 826 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 39(3):374-375 MOORE PSJ; CHUDLEY AE; WINTER JSD PITUITARY-GONADAL AXIS IN PREPUBERTAL BOYS WITH THE FRAGILE-X SYNDROME | 5 | 7 |
| 1147 | 1 | 15 | 832 1991 ANNALES DE GENETIQUE 34(2):111-114 BARLETTA C; RAGUSA RM; GAROFALO G; SCILLATO F; RUGGERI M SEGREGATION ANALYSIS OF AUTOSOMAL FRAGILE SITES IN 3 FAMILIES WITH THE FRAGILE X-CHROMOSOME | 0 | 5 |
| 1148 | 10 | 15 | 840 1991 CELL 66(4):817-822 PIERETTI M; ZHANG FP; FU YH; WARREN ST; OOSTRA BA; CASKEY CT; NELSON DL ABSENCE OF EXPRESSION OF THE FMR-1 GENE IN FRAGILE-X SYNDROME | 291 | 583 |
| 1149 | 4 | 15 | 866 1991 JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY 11(6):398-399 COHEN IL; TSIOURIS JA; PFADT A EFFECTS OF LONG-ACTING PROPRANOLOL ON AGONISTIC AND STEREOTYPED BEHAVIORS IN A MAN WITH PERVASIVE DEVELOPMENTAL DISORDER AND FRAGILE-X SYNDROME - A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY | 1 | 4 |
| 1150 | 10 | 15 | 933 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):208-216 DEVYS D; BIANCALANA V; ROUSSEAU F; BOUE J; MANDEL JL; OBERLE I ANALYSIS OF FULL FRAGILE-X MUTATIONS IN FETAL TISSUES AND MONOZYGOTIC TWINS INDICATE THAT ABNORMAL METHYLATION AND SOMATIC HETEROGENEITY ARE ESTABLISHED EARLY IN DEVELOPMENT | 58 | 89 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1151 | 12 | 15 | 938 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):282-290 TEJADA I; MORNET E; BIANCALANA V; OBERLE I; BOUE J; MANDEL JL; BOUE A DIRECT DNA ANALYSIS OF FRAGILE-X SYNDROME IN SPANISH PEDIGREES | 7 | 7 |
| 1152 | 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 |
| 1153 | 12 | 15 | 1063 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(6):687-688 LAIRD CD IMPRINTING AND IMPRINT ERASURE AS VIEWED THROUGH THE FRAGILE-X SYNDROME | 2 | 5 |
| 1154 | 4 | 15 | 1175 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):447-450 POMPONI MG; NERI G BUTYRATE AND ACETYL-CARNITINE INHIBIT THE CYTOGENETIC EXPRESSION OF THE FRAGILE-X IN-VITRO | 1 | 6 |
| 1155 | 2 | 15 | 1562 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):457-460 BillonGalland IO The fragile X syndrome and its clinical psychotic expression | 0 | 0 |
| 1156 | 9 | 15 | 1577 1997 CLINICAL GENETICS 52(3):147-154 Hecimovic S; Barisic I; Muller A; Petkovic I; Baric I; Ligutic I; Pavelic K Expand long PCR for fragile X mutation detection | 8 | 23 |
| 1157 | 6 | 15 | 1586 1997 GENETIC COUNSELING 8(1):1-6 Patsalis PC; Sismani C; Hadjimarcou MI; Rose N; Stylianidou G; Koukoulli R; Anastasiadou V; Deltas CC; Middleton L Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology | 1 | 3 |
| 1158 | 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 |
| 1159 | 10 | 15 | 1612 1997 JOURNAL OF MEDICAL GENETICS 34(11):924-926 Losekoot M; Hoogendoorn E; Olmer R; Jansen CCAM; Oosterwijk JC; vandenOuweland AMW; Halley DJJ; Warren ST; Willemsen R; Oostra BA; Bakker E Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus | 1 | 7 |
| 1160 | 4 | 15 | 1938 2000 JOURNAL OF PSYCHOEDUCATIONAL ASSESSMENT 18(3):255-267 Hooper SR; Hatton DD; Baranek GT; Roberts JP; Bailey DB Nonverbal assessment of IQ, attention, and memory abilities in children with fragile-X syndrome using the Leiter-R | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1161 | 9 | 15 | 2062 2001 REVISTA DE NEUROLOGIA 33:S29-S32 Brun-Gasca C; Artigas-Pallares J Psycholinguistic aspects of fragile X chromosome syndrome | 0 | 1 |
| 1162 | 13 | 15 | 2198 2002 TRENDS IN MOLECULAR MEDICINE 8(3):102-103 Oostra BA Functions of the fragile X protein | 6 | 8 |
| 1163 | 11 | 15 | 2241 2003 ARCHIVES DE PEDIATRIE 10(5):401-402 Ramos FJ; Willemsen R Diagnosis of the Fragile X Syndrome by the analysis of FMRP expression in blood and hair roots | 0 | 0 |
| 1164 | 10 | 15 | 2338 2004 JOURNAL OF MEDICAL GENETICS 41(4) Tassone F; Hagerman RJ; Garcia-Arocena D; Khandjian EW; Greco CM; Hagerman PJ Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome | 0 | 0 |
| 1165 | 1 | 14 | 109 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(4):631-635 HOWARDPEEBLES PN; FINLEY WH SCREENING OF MENTALLY-RETARDED MALES FOR MACRO-ORCHIDISM AND THE FRAGILE-X CHROMOSOME | 16 | 22 |
| 1166 | 5 | 14 | 125 1983 CLINICAL GENETICS 23(4):311-317 GARDNER RJM; SMART RD; CORNELL JM; MERCKEL LM; BEIGHTON P THE FRAGILE X-CHROMOSOME IN A LARGE INDIAN KINDRED | 17 | 20 |
| 1167 | 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 |
| 1168 | 1 | 14 | 339 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):445-455 LEDBETTER DH; AIRHART SD; NUSSBAUM RL CAFFEINE ENHANCES FRAGILE-(X) EXPRESSION IN SOMATIC-CELL HYBRIDS | 5 | 18 |
| 1169 | 4 | 14 | 386 1986 HUMAN GENETICS 73(4):309-312 ARINAMI T; KONDO I; NAKAJIMA S FREQUENCY OF THE FRAGILE X-SYNDROME IN JAPANESE MENTALLY-RETARDED MALES | 23 | 29 |
| 1170 | 8 | 14 | 452 1987 HUMAN GENETICS 75(3):294-295 BROWN WT; SHERMAN SL; DOBKIN CS HYPOTHESIS REGARDING THE NATURE OF THE FRAGILE-X MUTATION - A REPLY | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1171 | 11 | 14 | 525 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):337-345 PURVISSMITH SG; LAING S; SUTHERLAND GR; BAKER E PRENATAL-DIAGNOSIS OF THE FRAGILE-X - THE AUSTRALASIAN EXPERIENCE | 0 | 14 |
| 1172 | 10 | 14 | 620 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):302-303 COHEN IL; BROWN WT; JENKINS EC; KRAWCZUN MS; FRENCH JH; RAGUTHU S; WOLFSCHEIN EG; SUDHALTER V; FISCH G; WISNIEWSKI K FRAGILE-X SYNDROME IN FEMALES WITH AUTISM | 13 | 16 |
| 1173 | 9 | 14 | 630 1989 CLINICAL GENETICS 36(1):25-30 TUCKERMAN E; WEBB T THE INACTIVATION OF THE FRAGILE X-CHROMOSOME IN FEMALE CARRIERS OF THE MARTIN-BELL SYNDROME AS STUDIED BY 2 DIFFERENT METHODS | 4 | 6 |
| 1174 | 5 | 14 | 668 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(3):443-451 SVED JA; LAIRD CD POPULATION GENETIC CONSEQUENCES OF THE FRAGILE-X SYNDROME, BASED ON THE X-INACTIVATION IMPRINTING MODEL | 12 | 22 |
| 1175 | 1 | 14 | 691 1990 BRAIN & DEVELOPMENT 12(1):128-130 WAHLSTROM J; WITTENGERSTROM I; MELLQUIST L; ANVRET M; ODEN A THE RETT SYNDROME RELATED TO FRAGILE-X(P22) IN CAFFEINE-INDUCED LYMPHOCYTE CULTURE | 0 | 13 |
| 1176 | 2 | 14 | 692 1990 BRITISH DENTAL JOURNAL 168(4):160-162 NUNN JH; DURNING P FRAGILE-X (MARTIN BELL) SYNDROME AND DENTAL-CARE | 0 | 0 |
| 1177 | 5 | 14 | 701 1990 HUMAN GENETICS 84(3):263-266 ROUSSEAU F; VINCENT A; OBERLE I; MANDEL JL NEW INFORMATIVE POLYMORPHISM AT THE DXS304 LOCUS, A CLOSE DISTAL MARKER FOR THE FRAGILE X-LOCUS | 4 | 19 |
| 1178 | 11 | 14 | 785 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):269-274 CRONISTER A; SCHREINER R; WITTENBERGER M; AMIRI K; HARRIS K; HAGERMAN RJ HETEROZYGOUS FRAGILE-X FEMALE - HISTORICAL, PHYSICAL, COGNITIVE, AND CYTOGENETIC FEATURES | 36 | 54 |
| 1179 | 9 | 14 | 792 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):319-321 DAHL N; MALMGREN H; PETTERSSON U; HOLMGREN G; SEEMANOVA E; GUSTAVSON KH CARRIER DETECTION OF THE FRAGILE-X SYNDROME USING FLANKING LOCI DXS98, DXS105, AND DXS304 | 0 | 0 |
| 1180 | 11 | 14 | 882 1991 NATURE 349(6310):624-626 VINCENT A; HEITZ D; PETIT C; KRETZ C; OBERLE I; MANDEL JL ABNORMAL PATTERN DETECTED IN FRAGILE-X PATIENTS BY PULSED-FIELD GEL-ELECTROPHORESIS | 105 | 164 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1181 | 8 | 14 | 904 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(2):184-186 FINUCANE BM; JAEGER E; DUNN E; SCOTT CI STUDY OF COLOR-VISION IN FRAGILE-X SYNDROME | 1 | 1 |
| 1182 | 1 | 14 | 914 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):78-86 MAZZOCCO MMM; HAGERMAN RJ; PENNINGTON BF PROBLEM-SOLVING LIMITATIONS AMONG CYTOGENETICALLY EXPRESSING FRAGILE-X WOMEN | 23 | 31 |
| 1183 | 10 | 14 | 921 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):136-141 JENKINS EC; GENOVESE MJ; DUNCAN CJ; GU H; STARKHOUCK SL; LELE K; LI SY; KRAWCZUN MS FRA(X)(Q27.2), THE COMMON FRAGILE SITE, OBSERVED IN ONLY ONE OF 760 CASES STUDIED FOR THE FRAGILE-X SYNDROME | 1 | 1 |
| 1184 | 4 | 14 | 957 1992 AMERICAN JOURNAL ON MENTAL RETARDATION 96(5):528-535 MERYASH DL CHARACTERISTICS OF FRAGILE-X RELATIVES WITH DIFFERENT ATTITUDES TOWARD TERMINATING AN AFFECTED PREGNANCY | 4 | 5 |
| 1185 | 8 | 14 | 1021 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(6):605-606 GOLDSON E; HAGERMAN RJ FRAGILE-X SYNDROME AND FAILURE-TO-THRIVE | 4 | 4 |
| 1186 | 4 | 14 | 1079 1993 CLINICAL GENETICS 44(2):82-88 LOESCH DZ; SAMPSON ML EFFECT OF THE FRAGILE-X ANOMALY ON BODY PROPORTIONS ESTIMATED BY PEDIGREE ANALYSIS | 3 | 3 |
| 1187 | 8 | 14 | 1092 1993 HUMAN GENETICS 91(1):80-82 DREESEN JCFM; VANDENHURK JAJM; SMITS APT; VANDENOUWELAND AMW; MARKSLAG PWB; VANOOST BA DXS539, A POLYMORPHIC DNA MARKER PROXIMAL OF THE FRAGILE-X GENE | 0 | 2 |
| 1188 | 2 | 14 | 1365 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:326-330 SIMON EW; RAPPAPORT DA; PAPKA M; WOODRUFFPAK DS FRAGILE-X AND DOWNS-SYNDROME - ARE THERE SYNDROME-SPECIFIC COGNITIVE PROFILES AT LOW IQ LEVELS | 2 | 4 |
| 1189 | 11 | 14 | 1384 1995 NEW ZEALAND MEDICAL JOURNAL 108(1009):404-406 NEVILLE L; COCHRANE J; FITZGERALD P; KENNEDY M FRAGILE-X MENTAL-RETARDATION SYNDROME - DNA DIAGNOSIS AND CARRIER DETECTION IN NEW-ZEALAND FAMILIES | 0 | 0 |
| 1190 | 10 | 14 | 1437 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):362-364 Fisch GS; Carpenter N; HowardPeebles PN; Maddalena A; Simensen R; Tarleton J; JulienInalsingh C; Chalifoux M; Holden JJA Lack of association between mutation size and cognitive/behavior deficits in fragile X males: A brief report | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1191 | 7 | 14 | 1479 1996 GENETIC COUNSELING 7(4):245-247 Fryns JP Ovarian function in fragile X carriers | 0 | 0 |
| 1192 | 12 | 14 | 1496 1996 JOURNAL OF PEDIATRICS 129(4):611-614 Giangreco CA; Steele MW; Aston CE; Cummins JH; Wenger SL A simplified six-item checklist for screening for fragile X syndrome in the pediatric population | 10 | 20 |
| 1193 | 12 | 14 | 1506 1996 PEDIATRIC NEUROLOGY 15(4):358-360 Kluger G; Bohm I; Laub MC; Waldenmaier C Epilepsy and fragile X gene mutations | 6 | 12 |
| 1194 | 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 |
| 1195 | 11 | 14 | 1578 1997 CLINICAL GENETICS 52(4):211-215 Arvio M; Peippo M; Simola KOJ Applicability of a checklist for clinical screening of the fragile X syndrome | 10 | 13 |
| 1196 | 12 | 14 | 1648 1998 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 40(1):62-64 Gringras P; Barnicoat A Retesting for fragile X syndrome in cytogenetically normal males | 1 | 3 |
| 1197 | 7 | 14 | 1741 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):342-346 Jenkins EC; Wen GY; Kim KS; Zhong N; Sapienza VJ; Hong H; Chen J; Li SY; Houck GE; Ding XH; Nolin SL; Dobkin CS; Brown WT Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies | 2 | 2 |
| 1198 | 10 | 14 | 1742 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):347-349 Chiurazzi P; Pomponi MG; Sharrock A; Macpherson J; Lormeau S; Morel ML; Rousseau F DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature | 2 | 10 |
| 1199 | 10 | 14 | 1748 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):214-216 Pekarik V; Blazkova M; Kozak L Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic | 1 | 3 |
| 1200 | 10 | 14 | 1761 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):311-316 Grasso M; Faravelli F; Lo Nigro C; Chiurazzi P; Sperandeo MP; Argusti A; Pomponi MG; Lecora M; Sebastio GF; Perroni L; Andria G; Neri G; Bricarelli FD Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients | 1 | 1 |
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