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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
Page 2: 1 (A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT) 2 (AMERICAN JOURNAL OF HUMAN GENETICS) 3 (AMERICAN JOURNAL OF HUMAN GENETICS) 4 (AMERICAN JOURNAL OF HUMAN GENETICS) 5 (AMERICAN JOURNAL OF MEDICAL GENETICS) 6 (AMERICAN JOURNAL OF MEDICAL GENETICS) 7 (AMERICAN JOURNAL OF MEDICAL GENETICS) 8 (AMERICAN JOURNAL OF MEDICAL GENETICS) 9 (AMERICAN JOURNAL OF MEDICAL GENETICS) 10 (ANNALS OF NEUROLOGY) 11 (BIOPHYSICAL JOURNAL) 12 (CLINICAL GENETICS) 13 (CURRENT BIOLOGY) 14 (DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY) 15 (GENETIC TESTING) 16 (HUMAN GENETICS) 17 (JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION) 18 (JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS) 19 (JOURNAL OF MEDICAL GENETICS) 20 (JOURNAL OF NEUROSCIENCE RESEARCH) 21 (MEDICAL ANTHROPOLOGY QUARTERLY) 22 (NATURE REVIEWS NEUROSCIENCE) 23 (PEDIATRIC RESEARCH) 24 (REVISTA DE NEUROLOGIA)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 101 | 16 | 33 | 735 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(3):460-467 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; STEINBACH P; GLASS IA; SCHWARTZ CE; VANOOST BA; THIBODEAU SN; HAITES NE; OOSTRA BA; GINE R; CARBALLO M; MORRIS CP; HOPWOOD JJ; SUTHERLAND GR GENETIC-MAPPING OF NEW DNA PROBES AT XQ27 DEFINES A STRATEGY FOR DNA STUDIES IN THE FRAGILE-X SYNDROME | 30 | 47 |
| 102 | 0 | 1 | 736 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(4):815-815 FINUCANE B; SCOTT CI; KURTZ MB CONCURRENCE OF DOMINANT PIEBALD TRAIT AND FRAGILE X-SYNDROME | 0 | 2 |
| 103 | 6 | 17 | 737 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(6):1051-1057 RICHARDS RI; SHEN Y; HOLMAN K; KOZMAN H; HYLAND VJ; MULLEY JC; SUTHERLAND GR FRAGILE-X SYNDROME - DIAGNOSIS USING HIGHLY POLYMORPHIC MICROSATELLITE MARKERS | 14 | 40 |
| 104 | 17 | 34 | 738 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(2):279-288 REISS AL; FREUND L; TSENG JE; JOSHI PK NEUROANATOMY IN FRAGILE-X FEMALES - THE POSTERIOR-FOSSA | 43 | 64 |
| 105 | 10 | 22 | 739 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(3):656-661 KREMER EJ; YU S; PRITCHARD M; NAGARAJA R; HEITZ D; LYNCH M; BAKER E; HYLAND VJ; LITTLE RD; WADA M; TONIOLO D; VINCENT A; ROUSSEAU F; SCHLESSINGER D; SUTHERLAND GR; RICHARDS RI ISOLATION OF A HUMAN DNA-SEQUENCE WHICH SPANS THE FRAGILE-X | 16 | 32 |
| 106 | 0 | 0 | 740 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):35-35 TURNER G FRAGILE X-SYNDROME | 0 | 0 |
| 107 | 0 | 1 | 741 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 SCHLESSINGER D; ZUCCHI I; NAGARAJA R; LITTLE RD; ABIDI F; FREIJE D; PILIA G; PORTA G; YOON JY; JOHNSON SK; PALMIERI G; MONTANARO V; ROMANO G; CASAMASSIMI A; CICCODICOLA A; DURSO M CLONING OF THE FRAGILE-X LOCUS IN THE CONTEXT OF YEAST ARTIFICIAL CHROMOSOME-BASED MAPPING OF XQ24-28 | 0 | 0 |
| 108 | 0 | 0 | 742 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 POUSTKA A; DIETRICH A; KORN B; GROSS B; MONACO A; TONIOLO D; WARREN S; LEHRACH H MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION | 0 | 0 |
| 109 | 0 | 0 | 743 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 |
| 110 | 0 | 0 | 744 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):76-76 OBERLE I; ROUSSEAU F; HEITZ D; DEVYS D; ZENGERLING S; MANDEL JL MOLECULAR-BASIS OF THE FRAGILE-X SYNDROME AND DIAGNOSTIC APPLICATIONS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 111 | 0 | 0 | 745 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):76-76 YU S; KREMER E; PRITCHARD M; LYNCH M; NANCARROW J; BAKER E; HOLMAN K; MULLEY JC; WARREN ST; SCHLESSINGER D; RICHARDS RI; SUTHERLAND GR THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 0 | 0 |
| 112 | 0 | 0 | 746 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 |
| 113 | 0 | 0 | 747 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 |
| 114 | 0 | 0 | 748 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 |
| 115 | 0 | 0 | 749 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):159-159 REISS A; FREUND L; AYLWARD E NEUROANATOMY OF THE FRAGILE X SYNDROME | 0 | 0 |
| 116 | 0 | 0 | 750 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 |
| 117 | 0 | 0 | 751 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 |
| 118 | 0 | 0 | 752 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):211-211 BROWN WT; GOONEWARDENA P; RAY J; MIEZEJESKI C; KRAWCZUN M; JENKINS E PRENATALLY DETECTED FRAGILE X FEMALES - COUNSELING ISSUES AND LONG-TERM FOLLOW-UPS | 0 | 0 |
| 119 | 0 | 0 | 753 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 |
| 120 | 0 | 0 | 754 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):231-231 SHAPIRO LR; WILMOT PL PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE X-SYNDROME - DETERMINATION OF ACCURACY | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 121 | 0 | 0 | 755 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 |
| 122 | 0 | 0 | 756 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 |
| 123 | 0 | 0 | 757 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 |
| 124 | 0 | 0 | 758 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):269-269 PAJARES IL; DELICADO A; DETORRES ML; MARTIN VL; CASTROVIEJO IP; SOLERA J FRAGILE-X SYNDROME WITH EXTRAMICROCHROMOSOME | 0 | 0 |
| 125 | 0 | 0 | 759 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 |
| 126 | 0 | 1 | 760 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 |
| 127 | 0 | 0 | 761 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):273-273 RISCILE GR FRAGILE-X PATIENTS WITH ATYPICAL PHENOTYPES | 0 | 0 |
| 128 | 0 | 0 | 762 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):280-280 ZASLAV AL; BROWN WT THE SIGNIFICANCE OF LOW-LEVEL FRAGILE X EXPRESSION | 0 | 0 |
| 129 | 0 | 0 | 763 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):287-287 RAFI SK; SURANA RB; ANDERSON LH; CHRISTOPHER KL; WILSON B; MEHM WJ HYPEROXIA ENHANCES THE INDUCTION OF FRAGILE-X SITE OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 130 | 0 | 0 | 764 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):289-289 BUCKLEY D; JALAL S; DEWALD G FRAGILE-X STUDIES - WHAT IS PRACTICAL | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 131 | 0 | 0 | 765 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 |
| 132 | 0 | 0 | 766 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):290-290 JENKINS E; GENOVESE M; DUNCAN C; GU H; SCHWARTZRICHSTEIN C; STARKHOUCK S; LELE K; LI SY; KRAWCZUN M COMMON FRAGILE SITE FRA(X)(Q27.2), PRESENT IN ONLY 1 OF 685 CASES SCREENED FOR THE FRAGILE-X SYNDROME | 0 | 0 |
| 133 | 0 | 0 | 767 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 |
| 134 | 0 | 0 | 768 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 |
| 135 | 0 | 0 | 769 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 |
| 136 | 0 | 0 | 770 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 |
| 137 | 0 | 0 | 771 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 |
| 138 | 0 | 0 | 772 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):338-338 GLASS IA; DELMASTRO RG; LANYON WG; RAEBURN JA; KILPATRICK MW; CONNER JM IDENTIFICATION OF DIAGNOSTIC DNA MARKERS FOR THE FRAGILE-X SYNDROME | 0 | 0 |
| 139 | 0 | 0 | 773 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 |
| 140 | 0 | 0 | 774 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 141 | 0 | 0 | 775 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):357-357 RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; NELSON DL; VANOOST BA; SMITS APT; KUHL D; CASKEY CT; WARREN ST A FREQUENT DINUCLEOTIDE POLYMORPHISM OF THE FRAGILE-X BREAKPOINT CLUSTER REGION IS TIGHTLY LINKED TO THE FRAGILE-X SYNDROME LOCUS | 0 | 0 |
| 142 | 0 | 0 | 776 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 |
| 143 | 0 | 0 | 777 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):417-417 REINER O; VERKERK AJMH; PIERETTI M; PIZZUTI A; BLONDE L; NELSON D; OOSTRA B; CASKEY CT CHARACTERIZATION OF EXPRESSED SEQUENCES AT THE FRAGILE-X LOCUS | 0 | 0 |
| 144 | 0 | 0 | 778 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):469-469 FISCH GS; SHAPIRO LR; SIMENSEN R; SCHWARTZ CE; FRYNS JP; BORGHGRAEF M; CURFS LM; HOWARDPEEBLES PN; ARINAMI T; MAVROU A DIFFERENCES IN DECLINE IN IQ AMONG FRAGILE-X MALES - EVIDENCE FOR GENETIC-HETEROGENEITY | 0 | 0 |
| 145 | 0 | 0 | 779 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 |
| 146 | 15 | 30 | 901 1992 AMERICAN JOURNAL OF HUMAN GENETICS 50(5):968-980 YU S; MULLEY J; LOESCH D; TURNER G; DONNELLY A; GEDEON A; HILLEN D; KREMER E; LYNCH M; PRITCHARD M; SUTHERLAND GR; RICHARDS RI FRAGILE-X SYNDROME - UNIQUE GENETICS OF THE HERITABLE UNSTABLE ELEMENT | 93 | 174 |
| 147 | 5 | 29 | 902 1992 AMERICAN JOURNAL OF HUMAN GENETICS 50(5):1067-1076 LOESCH DZ; HUGGINS RM FIXED AND RANDOM EFFECTS IN THE VARIATION OF THE FINGER RIDGE COUNT - A STUDY OF FRAGILE-X FAMILIES | 7 | 8 |
| 148 | 18 | 23 | 903 1992 AMERICAN JOURNAL OF HUMAN GENETICS 51(2):299-306 WOHRLE D; KOTZOT D; HIRST MC; MANCA A; KORN B; SCHMIDT A; BARBI G; ROTT HD; POUSTKA A; DAVIES KE; STEINBACH P A MICRODELETION OF LESS THAN 250 KB, INCLUDING THE PROXIMAL PART OF THE FMR-I GENE AND THE FRAGILE-X SITE, IN A MALE WITH THE CLINICAL PHENOTYPE OF FRAGILE-X SYNDROME | 73 | 121 |
| 149 | 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 |
| 150 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 151 | 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 |
| 152 | 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 |
| 153 | 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 |
| 154 | 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 |
| 155 | 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 |
| 156 | 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 |
| 157 | 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 |
| 158 | 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 |
| 159 | 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 |
| 160 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 161 | 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 |
| 162 | 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 |
| 163 | 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 |
| 164 | 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 |
| 165 | 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 |
| 166 | 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 |
| 167 | 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 |
| 168 | 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 |
| 169 | 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 |
| 170 | 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 |
| 171 | 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 |
| 172 | 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 |
| 173 | 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 |
| 174 | 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 |
| 175 | 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 |
| 176 | 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 |
| 177 | 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 |
| 178 | 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 |
| 179 | 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 |
| 180 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 181 | 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 |
| 182 | 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 |
| 183 | 14 | 29 | 1150 1994 AMERICAN JOURNAL OF HUMAN GENETICS 54(3):437-442 KRUYER H; MILA M; GLOVER G; CARBONELL P; BALLESTA F; ESTIVILL X FRAGILE X SYNDROME AND THE (CGG)(N) MUTATION - 2 FAMILIES WITH DISCORDANT MZ TWINS | 20 | 59 |
| 184 | 30 | 38 | 1151 1994 AMERICAN JOURNAL OF HUMAN GENETICS 55(2):225-237 ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; MALMGREN H; DAHL N; BARNICOAT A; MATHEW C; MORNET E; TEJADA I; MADDALENA A; SPIEGEL R; SCHINZEL A; MARCOS JAG; SCHORDERET DF; SCHAAP T; MACCIONI L; RUSSO S; JACOBS PA; SCHWARTZ C; MANDEL JL A MULTICENTER STUDY ON GENOTYPE-PHENOTYPE CORRELATIONS IN THE FRAGILE-X-SYNDROME, USING DIRECT DIAGNOSIS WITH PROBE STB-12.3 - THE FIRST 2,253 CASES | 119 | 165 |
| 185 | 20 | 37 | 1259 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1042-1051 QUAN F; ZONANA J; GUNTER K; PETERSON KL; MAGENIS RE; POPOVICH BW AN ATYPICAL CASE OF FRAGILE-X SYNDROME CAUSED BY A DELETION THAT INCLUDES THE FMRI GENE | 16 | 29 |
| 186 | 18 | 65 | 1260 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1147-1155 FISCH GS; SNOW K; THIBODEAU SN; CHALIFAUX M; HOLDEN JJA; NELSON DL; HOWARDPEEBLES PN; MADDALENA A THE FRAGILE-X PREMUTATION IN CARRIERS AND ITS EFFECT ON MUTATION SIZE IN OFFSPRING | 24 | 34 |
| 187 | 19 | 51 | 1261 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(2):351-361 ZHONG N; YANG WH; DOBKIN C; BROWN WT FRAGILE-X GENE INSTABILITY - ANCHORING AGGS AND LINKED MICROSATELLITES | 38 | 79 |
| 188 | 35 | 54 | 1262 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(3):609-618 DEGRAAFF E; WILLEMSEN R; ZHONG N; DEDIESMULDERS CEM; BROWN WT; FRELING G; OOSTRA B INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF THE FMR1 PROTEIN IN A MALE FRAGILE-X PATIENT WITH A LUNG-TUMOR | 22 | 31 |
| 189 | 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 |
| 190 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 191 | 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 |
| 192 | 0 | 0 | 1266 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):153-153 BLACK SH; LEVINSON G; HARTON GL; PALMER FT; SISSON ME; SCHOENER C; NANCE C; FUGGER EF; FIELDS RA PREIMPLANTATION GENETIC TESTING (PGT) FOR FRAGILE-X (FRAX) | 2 | 3 |
| 193 | 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 |
| 194 | 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 |
| 195 | 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 |
| 196 | 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 |
| 197 | 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 |
| 198 | 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 |
| 199 | 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 |
| 200 | 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 |
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