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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by year, source, volume, issue, page.
Page 11: 1 (1) 2 (101) 3 (201) 4 (301) 5 (401) 6 (501) 7 (601) 8 (701) 9 (801) 10 (901) 11 (1001) 12 (1101) 13 (1201) 14 (1301) 15 (1401) 16 (1501) 17 (1601) 18 (1701) 19 (1801) 20 (1901) 21 (2001) 22 (2101) 23 (2201) 24 (2301)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1001 | 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 |
| 1002 | 17 | 25 | 1002 1992 MEDICINA CLINICA 98(4):121-124 GINE R; ESPINAS ML; ANTICH J; CARBALLO M MOLECULAR-GENETICS OF THE FRAGILE-X SYNDROME - MOLECULAR DIAGNOSIS BY DNA PROBES | 1 | 1 |
| 1003 | 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 |
| 1004 | 12 | 17 | 1004 1992 MENTAL RETARDATION 30(6):355-361 KEENAN J; KASTNER T; NATHANSON R; RICHARDSON N; HINTON J; CRESS DA A STATEWIDE PUBLIC AND PROFESSIONAL-EDUCATION PROGRAM ON FRAGILE X SYNDROME | 0 | 2 |
| 1005 | 0 | 0 | 1005 1992 MONATSSCHRIFT KINDERHEILKUNDE 140(7):404-404 KRUSE K GIRLS WITH FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) | 0 | 0 |
| 1006 | 11 | 16 | 1006 1992 NATURE GENETICS 1(3):157-158 HAGERMAN R CLINICAL CONUNDRUMS IN FRAGILE-X SYNDROME | 7 | 8 |
| 1007 | 7 | 9 | 1007 1992 NATURE GENETICS 1(4):237-238 CHAKRAVARTI A FRAGILE-X FOUNDER EFFECT | 15 | 32 |
| 1008 | 8 | 20 | 1008 1992 NATURE GENETICS 1(4):257-260 RICHARDS RI; HOLMAN K; FRIEND K; KREMER E; HILLEN D; STAPLES A; BROWN WT; GOONEWARDENA P; TARLETON J; SCHWARTZ C; SUTHERLAND GR EVIDENCE OF FOUNDER CHROMOSOMES IN FRAGILE-X SYNDROME | 69 | 158 |
| 1009 | 10 | 23 | 1009 1992 NATURE GENETICS 1(5):341-344 GEDEON AK; BAKER E; ROBINSON H; PARTINGTON MW; GROSS B; MANCA A; KORN B; POUSTKA A; YU S; SUTHERLAND GR; MULLEY JC FRAGILE-X SYNDROME WITHOUT CCG AMPLIFICATION HAS AN FMR1 DELETION | 82 | 137 |
| 1010 | 18 | 33 | 1010 1992 PEDIATRIC NEUROLOGY 8(4):272-274 WONG VCN; LAM STS FRAGILE X POSITIVITY IN CHINESE CHILDREN WITH AUTISTIC SPECTRUM DISORDER | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1011 | 21 | 31 | 1011 1992 PEDIATRICS 89(3):395-400 HAGERMAN RJ; JACKSON C; AMIRI K; SILVERMAN AC; OCONNOR R; SOBESKY W GIRLS WITH FRAGILE-X SYNDROME - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 57 | 79 |
| 1012 | 10 | 23 | 1012 1992 PEDIATRICS 89(6):1059-1062 BUTLER MG; BRUNSCHWIG A; MILLER LK; HAGERMAN RJ STANDARDS FOR SELECTED ANTHROPOMETRIC MEASUREMENTS IN MALES WITH THE FRAGILE X-SYNDROME | 24 | 28 |
| 1013 | 0 | 0 | 1013 1992 PEDIATRIE 47(11):743-750 PELLISSIER MC; VOELCKEL MA; MATTEI JF FRAGILE-X SYNDROME - CURRENT KNOWLEDGE | 0 | 0 |
| 1014 | 7 | 17 | 1014 1992 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 89(9):4215-4217 MORTON NE; MACPHERSON JN POPULATION-GENETICS OF THE FRAGILE-X SYNDROME - MULTIALLELIC MODEL FOR THE FMR1 LOCUS | 47 | 78 |
| 1015 | 27 | 59 | 1015 1992 PSYCHIATRIC GENETICS 2(4):277-300 BOLTON P; PICKLES A; BUTLER L; SUMMERS D; WEBB T; LORD C; LECOUTEUR A; BAILEY A; RUTTER M FRAGILE-X IN FAMILIES MULTIPLEX FOR AUTISM AND RELATED PHENOTYPES - PREVALENCE AND CRITERIA FOR CYTOGENETIC DIAGNOSIS | 1 | 7 |
| 1016 | 16 | 34 | 1016 1992 REMEDIAL AND SPECIAL EDUCATION 13(2):32-39 SANTOS KE FRAGILE X-SYNDROME - AN EDUCATORS ROLE IN IDENTIFICATION, PREVENTION, AND INTERVENTION | 0 | 2 |
| 1017 | 26 | 44 | 1017 1992 TRENDS IN GENETICS 8(7):249-255 RICHARDS RI; SUTHERLAND GR FRAGILE X-SYNDROME - THE MOLECULAR PICTURE COMES INTO FOCUS | 13 | 39 |
| 1018 | 19 | 26 | 1018 1992 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 20(2):113-120 VONGONTARD A; HILLIG U; HEROLD D CLINICAL AND CYTOGENETIC PROBLEMS IN THE DIAGNOSIS OF THE FRAGILE-X SYNDROME | 1 | 1 |
| 1019 | 4 | 9 | 1019 1992 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 92(4):28-31 LASTOCHKINA NA; KUPRIYANOVA TA; PUCHINSKAYA LM; MARINCHEVA GS; GORKOVA SA THE CLINICOELECTROPHYSIOLOGICAL CHARACTERIZATION OF WOMEN, HETEROZYGOUS CARRIERS OF FRAGILE X-CHROMOSOME | 1 | 1 |
| 1020 | 0 | 0 | 1020 1993 AMERICAN FAMILY PHYSICIAN 47(5):1072-1073 SIMENSEN RJ FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1021 | 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 |
| 1022 | 20 | 27 | 1022 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(7):723-726 STALEY LW; HULL CE; MAZZOCCO MMM; THIBODEAU SN; SNOW K; WILSON VL; TAYLOR A; MCGAVRAN L; WEINER D; RIDDLE J; OCONNOR R; HAGERMAN RJ MOLECULAR-CLINICAL CORRELATIONS IN CHILDREN AND ADULTS WITH FRAGILE X-SYNDROME | 21 | 24 |
| 1023 | 23 | 29 | 1023 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(11):1231-1235 RAMOS FJ; EUNPU DL; FINUCANE B; PFENDNER EG DIRECT DNA TESTING FOR FRAGILE-X SYNDROME | 1 | 2 |
| 1024 | 29 | 36 | 1024 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(11):1236-1241 HULL C; HAGERMAN RJ A STUDY OF THE PHYSICAL, BEHAVIORAL, AND MEDICAL PHENOTYPE, INCLUDING ANTHROPOMETRIC MEASURES, OF FEMALES WITH FRAGILE-X SYNDROME | 27 | 38 |
| 1025 | 13 | 23 | 1025 1993 AMERICAN JOURNAL OF HUMAN GENETICS 52(2):297-304 OUDET C; MORNET E; SERRE JL; THOMAS F; LENTESZENGERLING S; KRETZ C; DELUCHAT C; TEJADA I; BOUE J; BOUE A; MANDEL JL LINKAGE DISEQUILIBRIUM BETWEEN THE FRAGILE-X MUTATION AND 2 CLOSELY LINKED CA REPEATS SUGGESTS THAT FRAGILE-X CHROMOSOMES ARE DERIVED FROM A SMALL NUMBER OF FOUNDER CHROMOSOMES | 49 | 111 |
| 1026 | 23 | 47 | 1026 1993 AMERICAN JOURNAL OF HUMAN GENETICS 52(5):884-894 REISS AL; FREUND L; ABRAMS MT; BOEHM C; KAZAZIAN H NEUROBEHAVIORAL EFFECTS OF THE FRAGILE-X PREMUTATION IN ADULT WOMEN - A CONTROLLED-STUDY | 70 | 95 |
| 1027 | 0 | 0 | 1027 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):3-3 ROUSSEAU F; REHEL R; ROUILLARD P; DEGRANDPRE P; MORGAN K; KHANDIJIAN EW MUTATIONAL PREVALENCE OF FRAGILE X-PREMUTATIONS IN 10,624 FEMALES FROM THE GENERAL-POPULATION BY SOUTHERN BLOTTING | 0 | 2 |
| 1028 | 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 |
| 1029 | 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 |
| 1030 | 0 | 0 | 1030 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):78-78 ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; PETTERSON U; MATHEW C; MORNET E; MADDALENA A; SCHINZEL A; MARCOS JAG; SCHORDERET DF; SCHAAP T; MACCIONI L; RUSSO S; JACOBS PA; SCHWARTZ C; MANDEL JL A COLLABORATIVE MULTICENTER STUDY OF DIRECT DIAGNOSIS OF THE FRAGILE-X SYNDROME WITH PROBE STB12.3 - THE 1ST 2253 CASES | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1031 | 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 |
| 1032 | 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 |
| 1033 | 0 | 0 | 1033 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):144-144 HAGERMAN R; HULL C; CARPENTER I; STALEY L; OCONNOR R; SEYDEL C; MAZZOCCO M; TAYLOR A HIGH-FUNCTIONING FRAGILE X MALES | 1 | 1 |
| 1034 | 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 |
| 1035 | 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 |
| 1036 | 0 | 0 | 1036 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):448-448 HOLDEN JJA; CHALIFOUX M; WING M; WHITE BN; GLOVER T; STEIN C; ZEESMAN S; CHITAYAT D; TESHIMA I; BROWN C; WARREN ST THE FRAGILE-X SYNDROME AND PREMATURE MENOPAUSE | 1 | 1 |
| 1037 | 0 | 0 | 1037 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):465-465 KRUYER H; MILA M; GLOVER G; CASTELLVBEL S; CARBONELL P; VOLPINI V; ESTIVILL X MONOZYGOTIC TWINS DISCORDANT FOR THE FRAGILE-X SYNDROME (FXS) | 0 | 2 |
| 1038 | 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 |
| 1039 | 0 | 0 | 1039 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):678-678 EBERHART DE; WARREN ST ABNORMAL CHROMATIN STRUCTURE ASSOCIATED WITH THE FULL FRAGILE-X MUTATION | 1 | 2 |
| 1040 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1041 | 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 |
| 1042 | 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 |
| 1043 | 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 |
| 1044 | 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 |
| 1045 | 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 |
| 1046 | 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 |
| 1047 | 0 | 0 | 1047 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1208-1208 NOLIN SL; HOUCK GE; LI SY; DING XH; BROWN WT; DOBKIN CS MOSAICISM IN FRAGILE-X AFFECTED MALES | 0 | 2 |
| 1048 | 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 |
| 1049 | 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 |
| 1050 | 0 | 0 | 1050 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1241-1241 TORRES W; SAHOTA A; BOYADJIEV S; VANCE GH; WEAVER DD FRAGILE-X FULL MUTATION IN 2 CLINICALLY UNAFFECTED BROTHERS | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1051 | 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 |
| 1052 | 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 |
| 1053 | 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 |
| 1054 | 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 |
| 1055 | 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 |
| 1056 | 23 | 41 | 1056 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(4):800-809 MCCONKIEROSELL A; LACHIEWICZ AM; SPIRIDIGLIOZZI GA; TARLETON J; SCHOENWALD S; PHELAN MC; GOONEWARDENA P; DING XH; BROWN WT EVIDENCE THAT METHYLATION OF THE FMR-I LOCUS IS RESPONSIBLE FOR VARIABLE PHENOTYPIC-EXPRESSION OF THE FRAGILE-X SYNDROME | 63 | 99 |
| 1057 | 17 | 35 | 1057 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(5):1064-1073 LOESCH DZ; HUGGINS R; HAY DA; GEDEON AK; MULLEY JC; SUTHERLAND GR GENOTYPE-PHENOTYPE RELATIONSHIPS IN FRAGILE-X SYNDROME - A FAMILY STUDY | 43 | 60 |
| 1058 | 22 | 34 | 1058 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(6):1217-1228 SNOW K; DOUD LK; HAGERMAN R; PERGOLIZZI RG; ERSTER SH; THIBODEAU SN ANALYSIS OF A CGG SEQUENCE AT THE FMR-I LOCUS IN FRAGILE-X FAMILIES AND IN THE GENERAL-POPULATION | 84 | 136 |
| 1059 | 5 | 23 | 1059 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(1):81-87 BERRYKRAVIS E; SKLENA P DEMONSTRATION OF ABNORMAL CYCLIC-AMP PRODUCTION IN PLATELETS FROM PATIENTS WITH FRAGILE-X SYNDROME | 11 | 14 |
| 1060 | 13 | 25 | 1060 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(5):589-593 MILUNSKY A; HUANG XL; AMOS JA; HERSKOWITZ J; FARRER LA; WYANDT HE 46,XY/47,XYY MALE WITH THE FRAGILE X-SYNDROME - CYTOGENETIC AND MOLECULAR STUDIES | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1061 | 6 | 26 | 1061 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(4):415-422 LOESCH DZ; HUGGINS RM; CHIN WF EFFECT OF FRAGILE-X ON PHYSICAL AND INTELLECTUAL TRAITS ESTIMATED BY PEDIGREE ANALYSIS | 7 | 9 |
| 1062 | 1 | 11 | 1062 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(6):685-686 MIGEON BR ROLE OF DNA METHYLATION IN X-INACTIVATION AND THE FRAGILE X-SYNDROME | 2 | 3 |
| 1063 | 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 |
| 1064 | 4 | 9 | 1064 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 47(2):216-220 WIEGERS AM; CURFS LMG; VERMEER ELMH; FRYNS JP ADAPTIVE-BEHAVIOR IN THE FRAGILE X-SYNDROME - PROFILE AND DEVELOPMENT | 5 | 6 |
| 1065 | 60 | 138 | 1065 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 48(2):112-121 FISCH GS WHAT IS ASSOCIATED WITH THE FRAGILE-X SYNDROME | 21 | 34 |
| 1066 | 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 |
| 1067 | 0 | 0 | 1067 1993 ANNALES DE PEDIATRIE 40(9):565-572 BLANC DS; DANGELO J; ETANGS NLD AUTISM AND THE FRAGILE X-SYNDROME | 1 | 1 |
| 1068 | 42 | 66 | 1068 1993 ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE 117(11):1121-1125 TSONGALIS GJ; SILVERMAN LM MOLECULAR PATHOLOGY OF THE FRAGILE-X SYNDROME | 0 | 2 |
| 1069 | 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 |
| 1070 | 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 |
| 1071 | 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 |
| 1072 | 5 | 17 | 1072 1993 BIOLOGICAL PSYCHIATRY 33(3):213-216 JEFFRIES FM; REISS AL; BROWN WT; MEYERS DA; GLICKSMAN AC; BANDYOPADHYAY S BIPOLAR SPECTRUM DISORDER AND FRAGILE-X SYNDROME - A FAMILY STUDY | 4 | 13 |
| 1073 | 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 |
| 1074 | 1 | 8 | 1074 1993 BRITISH JOURNAL OF HAEMATOLOGY 85(2):415-416 VORST EJ; LEVENE NA; NISANI R; BERREBI A FRAGILE-X SYNDROME AND MYELODYSPLASIA DISCOVERED DURING PREGNANCY | 3 | 5 |
| 1075 | 18 | 52 | 1075 1993 CELL 73(7):1403-1409 HANSEN RS; CANFIELD TK; LAMB MM; GARTLER SM; LAIRD CD ASSOCIATION OF FRAGILE-X SYNDROME WITH DELAYED REPLICATION OF THE FMR1 GENE | 23 | 121 |
| 1076 | 15 | 56 | 1076 1993 CELL 74(2):291-298 SIOMI H; SIOMI MC; NUSSBAUM RL; DREYFUSS G THE PROTEIN PRODUCT OF THE FRAGILE-X GENE, FMR1, HAS CHARACTERISTICS OF AN RNA-BINDING PROTEIN | 117 | 315 |
| 1077 | 20 | 26 | 1077 1993 CLINICAL GENETICS 43(1):34-38 HORI T; YAMAUCHI M; SEKI N; TSUJI S; IKUKO K HERITABLE UNSTABLE DNA-SEQUENCES AND HYPERMETHYLATION ASSOCIATED WITH FRAGILE-X SYNDROME IN JAPANESE FAMILIES | 9 | 13 |
| 1078 | 7 | 7 | 1078 1993 CLINICAL GENETICS 43(3):157-159 MORNET E; JOKIC M; BOGYO A; TEJADA I; DELUCHAT C; BOUE J; BOUE A AFFECTED SIBS WITH FRAGILE-X SYNDROME EXHIBIT AN AGE-DEPENDENT DECREASE IN THE SIZE OF THE FRAGILE-X FULL MUTATION | 5 | 8 |
| 1079 | 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 |
| 1080 | 7 | 11 | 1080 1993 CLINICAL GENETICS 44(2):109-110 BODURTHA J; JACKSONCOOK C; MADDALENA A; PISERCHIO J; WALLER R 46XY/47XYY MOSAICISM AND FRAGILE-X | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1081 | 18 | 37 | 1081 1993 CLINICAL GENETICS 44(3):129-138 BUTLER MG; PRATESI R; WATSON MS; BREG WR; SINGH DN ANTHROPOMETRIC AND CRANIOFACIAL PATTERNS IN MENTALLY-RETARDED MALES WITH EMPHASIS ON THE FRAGILE-X SYNDROME | 4 | 8 |
| 1082 | 16 | 20 | 1082 1993 CLINICAL GENETICS 44(4):169-172 YAMAUCHI M; NAGATA S; SEKI N; TOYAMA Y; HARADA N; NIIKAWA N; MASUNO I; KAJII T; HORI T PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT-DETECTION OF THE DYNAMIC MUTATION DUE TO AN UNSTABLE DNA-SEQUENCE | 2 | 5 |
| 1083 | 16 | 34 | 1083 1993 CURRENT BIOLOGY 3(11):783-786 TROTTIER Y; DEVYS D; MANDEL JL FRAGILE-X SYNDROME - AN EXPANDING STORY | 4 | 8 |
| 1084 | 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 |
| 1085 | 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 |
| 1086 | 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 |
| 1087 | 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 |
| 1088 | 16 | 28 | 1088 1993 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 35(6):532-539 BARNICOAT AJ; DOCHERTY Z; BOBROW M WHERE HAVE ALL THE FRAGILE-X BOYS GONE | 4 | 6 |
| 1089 | 9 | 31 | 1089 1993 EUROPEAN JOURNAL OF HUMAN GENETICS 1(1):72-79 DEVRIES BBA; WIEGERS AM; DEGRAAFF E; VERKERK AJMH; VANHEMEL JO; HALLEY DJJ; FRYNS JP; CURFS LMG; NIERMEIJER MF; OOSTRA BA MENTAL STATUS AND FRAGILE-X EXPRESSION IN RELATION TO FMR-1 GENE MUTATION | 36 | 48 |
| 1090 | 38 | 84 | 1090 1993 GENETIC COUNSELING 4(4):245-263 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H FRAGILE-X SYNDROME AND AUTISM - A PREVALENT ASSOCIATION OR A MISINTERPRETED CONNECTION | 6 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1091 | 13 | 23 | 1091 1993 GENETIKA 29(6):1026-1034 BARANOV VS; ASEEV MV; RAKISHEVA ZB; KULESHOV NP; MARINICHEVA GS; BYCHKOVA AM; ZUKIN VD; LEDASCHEVA EA; AMOASHYI DS; KUZNETZOVA TV; VAHARLOVSKY VG MOLECULAR DIAGNOSIS OF FRAGILE X-SYNDROME (SYN MARTIN-BELL) IN THE PATIENTS OF NATIVE POPULATIONS | 0 | 2 |
| 1092 | 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 |
| 1093 | 14 | 31 | 1093 1993 HUMAN GENETICS 91(5):469-474 LOESCH DZ; SHEFFIELD LJ; HAY DA BETWEEN-GENERATION DIFFERENCES IN ASCERTAINMENT AND PENETRANCE - RELEVANCE TO GENETIC HYPOTHESES IN FRAGILE-X | 5 | 5 |
| 1094 | 16 | 27 | 1094 1993 HUMAN GENETICS 92(3):269-272 BUYLE S; REYNIERS E; VITS L; DEBOULLE K; HANDIG I; WUYTS FLE; DEELEN W; HALLEY DJJ; OOSTRA BA; WILLEMS PJ FOUNDER EFFECT IN A BELGIAN-DUTCH FRAGILE-X POPULATION | 19 | 29 |
| 1095 | 11 | 29 | 1095 1993 HUMAN GENETICS 92(4):373-378 MORNET E; BOGYO A; DELUCHAT C; SIMONBOUY B; MATHIEU M; THEPOT F; GRISARD MC; LEGUERN E; BOUE J; BOUE A MOLECULAR ANALYSIS OF A RING CHROMOSOME-X IN A FAMILY WITH FRAGILE-X SYNDROME | 0 | 1 |
| 1096 | 6 | 20 | 1096 1993 HUMAN GENETICS 92(5):431-436 ARINAMI T; ASANO M; KOBAYASHI K; YANAGI H; HAMAGUCHI H DATA ON THE CGG REPEAT AT THE FRAGILE X-SITE IN THE NONRETARDED JAPANESE POPULATION AND FAMILY SUGGEST THE PRESENCE OF A SUBGROUP OF NORMAL ALLELES PREDISPOSING TO MUTATE | 21 | 41 |
| 1097 | 35 | 45 | 1097 1993 HUMAN GENETICS 92(5):491-498 STEINBACH P; WOHRLE D; TARIVERDIAN G; KENNERKNECHT I; BARBI G; EDLINGER H; ENDERS H; GOTZSOTHMANN M; HEILBRONNER H; HOSENFELD D; KIRCHEISEN R; MAJEWSKI F; MEINECKE P; PASSARGE E; SCHMIDT A; SEIDEL H; WOLFF G; ZANKL M MOLECULAR ANALYSIS OF MUTATIONS IN THE GENE FMR-1 SEGREGATING IN FRAGILE X-FAMILIES | 7 | 11 |
| 1098 | 8 | 24 | 1098 1993 HUMAN MOLECULAR GENETICS 2(4):399-404 VERKERK AJMH; DEGRAAFF E; DEBOULLE K; EICHLER EE; KONECKI DS; REYNIERS E; MANCA A; POUSTKA A; WILLEMS PJ; NELSON DL; OOSTRA BA ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 | 0 | 75 |
| 1099 | 0 | 1 | 1099 1993 HUMAN MOLECULAR GENETICS 2(8):1348-1348 VERKERK AJMH; DEGRAAFF E; DEBOULLE K; EICHLER EE; KONECKI DS; REYNIERS E; MANCA A; POUSTKA A; WILLEMS PJ; NELSON DL; OOSTRA BA ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 (VOL 2, PG 399, 1993) | 3 | 6 |
| 1100 | 10 | 29 | 1100 1993 HUMAN MOLECULAR GENETICS 2(9):1429-1435 RICHARDS RI; HOLMAN K; YU S; SUTHERLAND GR FRAGILE-X SYNDROME UNSTABLE ELEMENT, P(CCG)N, AND OTHER SIMPLE TANDEM REPEAT SEQUENCES ARE BINDING-SITES FOR SPECIFIC NUCLEAR PROTEINS | 11 | 80 |
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