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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 13: 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 |
|---|---|---|---|---|---|
| 1201 | 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 |
| 1202 | 10 | 11 | 1202 1994 ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE 148(1):63-64 LEUNG AKC; MCLEOD DR; ROBSON WLM; FAGAN JE PICTURE OF THE MONTH - FRAGILE-X SYNDROME | 0 | 1 |
| 1203 | 14 | 28 | 1203 1994 BRITISH JOURNAL OF CLINICAL PRACTICE 48(1):42-44 PATEL BD THE FRAGILE-X SYNDROME | 1 | 1 |
| 1204 | 0 | 0 | 1204 1994 CANADIAN FAMILY PHYSICIAN 40:290-295 WIEBE E; WIEBE A FRAGILE-X SYNDROME | 0 | 1 |
| 1205 | 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 |
| 1206 | 15 | 39 | 1206 1994 CELL 77(1):33-39 SIOMI H; CHOI MY; SIOMI MC; NUSSBAUM RL; DREYFUSS G ESSENTIAL ROLE FOR KH DOMAINS IN RNA-BINDING - IMPAIRED RNA-BINDING BY A MUTATION IN THE KH DOMAIN OF FMR1 THAT CAUSES FRAGILE-X SYNDROME | 64 | 254 |
| 1207 | 20 | 53 | 1207 1994 CELL 77(6):853-861 KUNST CB; WARREN ST CRYPTIC AND POLAR VARIATION OF THE FRAGILE-X REPEAT COULD RESULT IN PREDISPOSING NORMAL ALLELES | 70 | 239 |
| 1208 | 22 | 52 | 1208 1994 CELL 78(1):23-33 BAKKER CE; VERHEIJ C; WILLEMSEN R; VANDERHELM R; OERLEMANS F; VERMEY M; BYGRAVE A; HOOGEVEEN AT; OOSTRA BA; REYNIERS E; DEBOULLE K; DHOOGE R; CRAS P; VANVELZEN D; NAGELS G; MARTIN JJ; DEDEYN PP; DARBY JK; WILLEMS PJ FMR1 KNOCKOUT MICE - A MODEL TO STUDY FRAGILE-X MENTAL-RETARDATION | 78 | 147 |
| 1209 | 10 | 23 | 1209 1994 CLINICAL GENETICS 45(4):175-180 SCHRANDERSTUMPEL C; GERVER WJ; MEYER H; ENGELEN J; MULDER H; FRYNS JP PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X SYNDROME | 4 | 17 |
| 1210 | 6 | 7 | 1210 1994 CLINICAL GENETICS 45(4):186-189 LOPEZPAJARES I; DELICADO A; PASCUALCASTROVIEJO I; LOPEZMARTIN V; MORENO F; GARCIAMARCOS JA FRAGILE-X SYNDROME WITH EXTRA MICROCHROMOSOME | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1211 | 19 | 64 | 1211 1994 DEVELOPMENTAL BRAIN DYSFUNCTION 7(2-3):155-164 HAGERMAN RJ; FULTON MJ; LEAMAN A; RIDDLE J; HAGERMAN K; SOBESKY W A SURVEY OF FLUOXETINE THERAPY IN FRAGILE-X SYNDROME | 16 | 18 |
| 1212 | 57 | 91 | 1212 1994 EUROPEAN JOURNAL OF CLINICAL INVESTIGATION 24(1):1-10 ROUSSEAU F THE FRAGILE-X SYNDROME - IMPLICATIONS OF MOLECULAR-GENETICS FOR THE CLINICAL SYNDROME | 7 | 10 |
| 1213 | 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 |
| 1214 | 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 |
| 1215 | 19 | 28 | 1215 1994 HUMAN GENETICS 93(2):143-147 VAISANEN ML; KAHKONEN M; LEISTI J DIAGNOSIS OF FRAGILE-X SYNDROME BY DIRECT MUTATION ANALYSIS | 9 | 12 |
| 1216 | 21 | 34 | 1216 1994 HUMAN GENETICS 94(4):395-400 MILA M; KRUYER H; GLOVER G; SANCHEZ A; CARBONELL P; CASTELLVIBEL S; VOLPINI V; ROSELL J; GABARRON J; LOPEZ I; VILLA M; BALLESTA F; ESTIVILL X MOLECULAR ANALYSIS OF THE (CGG)(N) EXPANSION IN THE FMR-1 GENE IN 59 SPANISH FRAGILE-X SYNDROME FAMILIES | 12 | 16 |
| 1217 | 13 | 19 | 1217 1994 HUMAN GENETICS 94(5):479-483 HAATAJA R; VAISANEN ML; LI MY; RYYNANEN M; LEISTI J THE FRAGILE-X SYNDROME IN FINLAND - DEMONSTRATION OF A FOUNDER EFFECT BY ANALYSIS OF MICROSATELLITE HAPLOTYPES | 11 | 19 |
| 1218 | 23 | 31 | 1218 1994 HUMAN MOLECULAR GENETICS 3(3):393-398 REISS AL; KAZAZIAN HH; KREBS CM; MCAUGHAN A; BOEHM CD; ABRAMS MT; NELSON DL FREQUENCY AND STABILITY OF THE FRAGILE-X PREMUTATION | 29 | 61 |
| 1219 | 20 | 28 | 1219 1994 HUMAN MOLECULAR GENETICS 3(3):399-405 MACPHERSON JN; BULLMAN H; YOUINGS SA; JACOBS PA INSERT SIZE AND FLANKING HAPLOTYPE IN FRAGILE-X AND NORMAL-POPULATIONS - POSSIBLE MULTIPLE ORIGINS FOR THE FRAGILE-X MUTATION | 28 | 57 |
| 1220 | 21 | 33 | 1220 1994 HUMAN MOLECULAR GENETICS 3(4):615-620 MEIJER H; DEGRAAFF E; MERCKX DML; JONGBLOED RJE; DEDIESMULDERS CEM; ENGELEN JJM; FRYNS JP; CURFS PMG; OOSTRA BA A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1 GENE CAUSES THE CLINICAL PHENOTYPE OF THE FRAGILE X SYNDROME | 46 | 78 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1221 | 17 | 29 | 1221 1994 HUMAN MOLECULAR GENETICS 3(9):1543-1551 SNOW K; TESTER DJ; KRUCKEBERG KE; SCHAID DJ; THIBODEAU SN SEQUENCE-ANALYSIS OF THE FRAGILE-X TRINUCLEOTIDE REPEAT - IMPLICATIONS FOR THE ORIGIN OF THE FRAGILE-X MUTATION | 47 | 115 |
| 1222 | 27 | 46 | 1222 1994 HUMAN MOLECULAR GENETICS 3(9):1553-1560 HIRST MC; GREWAL PK; DAVIES KE PRECURSOR ARRAYS FOR TRIPLET REPEAT EXPANSION AT THE FRAGILE-X LOCUS | 37 | 108 |
| 1223 | 7 | 18 | 1223 1994 INTELLIGENCE 19(1):45-50 DANIELS JK; OWEN MJ; MCGUFFIN P; THOMPSON L; DETTERMAN DK; CHORNEY M; CHORNEY K; SMITH D; SKUDER P; VIGNETTI S; MCCLEARN GE; PLOMIN R IQ AND VARIATION IN THE NUMBER OF FRAGILE-X CGG REPEATS - NO ASSOCIATION IN A NORMAL SAMPLE | 2 | 9 |
| 1224 | 1 | 5 | 1224 1994 ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES 15(7):365-368 MUSUMECI SA; ELIA M; FERRI R; SCUDERI C; DELGRACCO S EVOKED SPIKES AND GIANT SOMATOSENSORY-EVOKED POTENTIALS IN A PATIENT WITH FRAGILE-X SYNDROME | 3 | 8 |
| 1225 | 1 | 1 | 1225 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(1):28-28 BROWN WT; HOUCK GE; JEZIOROWSKA A; LEVINSON FN; DING X; DOBKIN C; ZHONG N; HENDERSON J; BROOKS SS; JENKINS EC RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST (VOL 270, PG 1569, 1993) | 1 | 1 |
| 1226 | 30 | 48 | 1226 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):507-514 TAYLOR AK; SAFANDA JF; FALL MZ; QUINCE C; LANG KA; HULL CE; CARPENTER I; STALEY LW; HAGERMAN RJ MOLECULAR PREDICTORS OF COGNITIVE INVOLVEMENT IN FEMALE CARRIERS OF FRAGILE-X SYNDROME | 76 | 89 |
| 1227 | 41 | 81 | 1227 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):536-542 WARREN ST; NELSON DL ADVANCES IN MOLECULAR ANALYSIS OF FRAGILE-X SYNDROME | 59 | 125 |
| 1228 | 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 |
| 1229 | 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 |
| 1230 | 10 | 23 | 1230 1994 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 24(4):473-485 MAZZOCCO MMM; PENNINGTON BF; HAGERMAN RJ SOCIAL COGNITION SKILLS AMONG FEMALES WITH FRAGILE-X | 9 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1231 | 0 | 0 | 1231 1994 JOURNAL OF CELLULAR BIOCHEMISTRY :184-184 WARREN ST OVERVIEW AND UPDATE ON FMR1 AND FRAGILE-X SYNDROME | 0 | 0 |
| 1232 | 9 | 20 | 1232 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:1-8 DEVRIES LBA; HALLEY DJJ; OOSTRA BA; NIERMEIJER MF THE FRAGILE-X SYNDROME - A GROWING GENE CAUSING FAMILIAL INTELLECTUAL DISABILITY | 1 | 2 |
| 1233 | 16 | 27 | 1233 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:27-35 SABARATNAM M; LAVER S; BUTLER L; PEMBREY M FRAGILE-X SYNDROME IN NORTH-EAST ESSEX - TOWARDS SYSTEMATIC SCREENING - CLINICAL-SELECTION | 6 | 8 |
| 1234 | 3 | 8 | 1234 1994 JOURNAL OF MEDICAL GENETICS 31(1):76-78 TEJADA MI; MORNET E; TIZZANO E; MOLINA M; BAIGET M; BOUE A IDENTIFICATION BY MOLECULAR DIAGNOSIS OF MOSAIC TURNERS-SYNDROME IN AN OBLIGATE CARRIER FEMALE FOR FRAGILE-X SYNDROME | 4 | 8 |
| 1235 | 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 |
| 1236 | 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 |
| 1237 | 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 |
| 1238 | 1 | 3 | 1238 1994 JOURNAL OF MEDICAL GENETICS 31(3):260-261 GILLESSENKAESBACH G; HORSTHEMKE B CLINICAL AND MOLECULAR STUDIES IN FRAGILE-X PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE | 0 | 3 |
| 1239 | 1 | 2 | 1239 1994 JOURNAL OF MEDICAL GENETICS 31(10):820-820 DEVRIES BBA; NIERMEIJER MF THE PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X PATIENTS - A DESIGNATION FACILITATING CLINICAL (AND MOLECULAR) DIFFERENTIAL-DIAGNOSIS | 1 | 6 |
| 1240 | 6 | 12 | 1240 1994 JOURNAL OF MEDICAL GENETICS 31(12):950-952 CURTIS G; DENNIS N; MACPHERSON J THE IMPACT OF GENETIC-COUNSELING ON FEMALES IN FRAGILE-X FAMILIES | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1241 | 2 | 44 | 1241 1994 JOURNAL OF MOLECULAR BIOLOGY 243(2):143-151 SMITH SS; LAAYOUN A; LINGEMAN RG; BAKER DJ; RILEY J HYPERMETHYLATION OF TELOMERE-LIKE FOLDBACKS AT CODON-12 OF THE HUMAN C-HA-RAS GENE AND THE TRINUCLEOTIDE REPEAT OF THE FMR-1 GENE OF FRAGILE-X | 10 | 54 |
| 1242 | 18 | 33 | 1242 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(2):247-255 SOBESKY WE; HULL CE; HAGERMAN RJ SYMPTOMS OF SCHIZOTYPAL PERSONALITY-DISORDER IN FRAGILE-X WOMEN | 17 | 32 |
| 1243 | 11 | 37 | 1243 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(2):256-264 DORN MB; MAZZOCCO MMM; HAGERMAN RJ BEHAVIORAL AND PSYCHIATRIC-DISORDERS IN ADULT MALE CARRIERS OF FRAGILE-X | 21 | 31 |
| 1244 | 15 | 18 | 1244 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(9):1316-1321 MERENSTEIN SA; SHYU V; SOBESKY WE; STALEY L; BERRYKRAVIS E; NELSON DL; LUGENBEEL KA; TAYLOR AK; PENNINGTON BF; HAGERMAN RJ FRAGILE-X SYNDROME IN A NORMAL IQ MALE WITH LEARNING AND EMOTIONAL-PROBLEMS | 18 | 22 |
| 1245 | 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 |
| 1246 | 2 | 5 | 1246 1994 LANCET 344(8935):1500-1500 TURNER G; ROBINSON H; WAKE S; MARTIN N DIZYGOUS TWINNING AND PREMATURE MENOPAUSE IN FRAGILE-X SYNDROME | 31 | 50 |
| 1247 | 2 | 2 | 1247 1994 MENTAL RETARDATION 32(2):156-156 SPITZ HH FRAGILE-X SYNDROME IS NOT THE 2ND LEADING CAUSE OF MENTAL-RETARDATION | 0 | 1 |
| 1248 | 4 | 8 | 1248 1994 MOLECULAR AND CELLULAR PROBES 8(2):177-180 CAO J; TARLETON J; BARBERIO D; DAVIDOW LS A SIMPLE FRAGILE-X PCR ASSAY WITH 7-DEAZAGUANINE-SUBSTITUTED DNA VISUALIZED BY ETHIDIUM-BROMIDE | 2 | 5 |
| 1249 | 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 |
| 1250 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1251 | 22 | 61 | 1251 1994 NEUROLOGY 44(7):1317-1324 REISS AL; LEE J; FREUND L NEUROANATOMY OF FRAGILE-X SYNDROME - THE TEMPORAL-LOBE | 49 | 83 |
| 1252 | 7 | 41 | 1252 1994 NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY 24(6):413-426 FERRI R; MUSUMECI SA; ELIA M; DELGRACCO S; SCUDERI C; BERGONZI P BIT-MAPPED SOMATOSENSORY-EVOKED POTENTIALS IN THE FRAGILE-X SYNDROME | 7 | 15 |
| 1253 | 0 | 0 | 1253 1994 PEDIATRIC RESEARCH 35(4):A23-A23 LACHIEWICZ AM; DAWSON DV AUTISTIC BEHAVIORS OF YOUNG GIRLS WITH FRAGILE X-SYNDROME | 1 | 1 |
| 1254 | 14 | 31 | 1254 1994 PEDIATRICS 93(6):992-995 LACHIEWICZ AM; DAWSON DV DO YOUNG BOYS WITH FRAGILE-X-SYNDROME HAVE MACROORCHIDISM | 13 | 17 |
| 1255 | 16 | 21 | 1255 1994 PRENATAL DIAGNOSIS 14(6):469-474 STRAIN L; PORTEOUS MEM; GOSDEN CM; ELLIS PM; NEILSON JP; BONTHRON DT PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION | 3 | 4 |
| 1256 | 10 | 30 | 1256 1994 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 91(11):4950-4954 FRY M; LOEB LA THE FRAGILE-X SYNDROME D(CGG)(N) NUCLEOTIDE REPEATS FORM A STABLE TETRAHELICAL STRUCTURE | 26 | 142 |
| 1257 | 2 | 11 | 1257 1994 THERIOGENOLOGY 42(5):789-794 LLAMBI S; POSTIGLIONI A LOCALIZATION OF THE FRAGILE-X CHROMOSOME BREAK POINTS IN HOLSTEIN-FRIESIAN CATTLE (BOS-TAURUS) | 0 | 2 |
| 1258 | 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 |
| 1259 | 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 |
| 1260 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1261 | 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 |
| 1262 | 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 |
| 1263 | 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 |
| 1264 | 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 |
| 1265 | 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 |
| 1266 | 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 |
| 1267 | 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 |
| 1268 | 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 |
| 1269 | 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 |
| 1270 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1271 | 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 |
| 1272 | 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 |
| 1273 | 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 |
| 1274 | 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 |
| 1275 | 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 |
| 1276 | 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 |
| 1277 | 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 |
| 1278 | 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 |
| 1279 | 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 |
| 1280 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1281 | 0 | 0 | 1281 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1395-1395 HART PS; OLSON SM; CRANDALL K; TARLETON J FRAGILE-X SYNDROME RESULTING FROM A 400 BASEPAIR DELETION WITHIN THE FMR1 GENE | 0 | 2 |
| 1282 | 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 |
| 1283 | 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 |
| 1284 | 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 |
| 1285 | 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 |
| 1286 | 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 |
| 1287 | 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 |
| 1288 | 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 |
| 1289 | 0 | 0 | 1289 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1941-1941 TSAI MS; CHIEN TY; YANG YL; CHEN HR; HWANG SM IDENTIFICATION OF THE NUMBER OF THE FRAGILE-X SYNDROME CGG REPEAT USING SILVER STAIN | 0 | 0 |
| 1290 | 11 | 21 | 1290 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(5):991-993 SHERMAN SL THE HIGH PREVALENCE OF FRAGILE-X PREMUTATION CARRIER FEMALES - IS THIS FREQUENCY UNIQUE TO THE FRENCH-CANADIAN POPULATION | 7 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1291 | 33 | 42 | 1291 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(5):1006-1018 ROUSSEAU F; ROUILLARD P; MOREL ML; KHANDJIAN EW; MORGAN K PREVALENCE OF CARRIERS OF PREMUTATION-SIZE ALLELES OF THE FMRI GENE AND IMPLICATIONS FOR THE POPULATION-GENETICS OF THE FRAGILE-X SYNDROME | 78 | 105 |
| 1292 | 20 | 27 | 1292 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1408-1413 LOESCH DZ; HUGGINS R; PETROVIC V; SLATER H EXPANSION OF THE CGG REPEAT IN FRAGILE-X IN THE FMR1 GENE DEPENDS ON THE SEX OF THE OFFSPRING | 5 | 12 |
| 1293 | 26 | 42 | 1293 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1414-1425 ASHLEY AE; SHERMAN SL POPULATION-DYNAMICS OF A MEIOTIC MITOTIC EXPANSION MODEL FOR THE FRAGILE-X SYNDROME | 13 | 20 |
| 1294 | 11 | 13 | 1294 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 55(3):384-386 PRIOR TW; PAPP AC; SNYDER PJ; SEDRA MS; GUIDA M; ENRILE BG GERMLINE MOSAICISM AT THE FRAGILE-X LOCUS | 2 | 7 |
| 1295 | 2 | 5 | 1295 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 57(3):508-509 LAXOVA R FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 2 | 3 |
| 1296 | 16 | 33 | 1296 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 58(3):249-256 LOESCH DZ; HUGGINS RM; HOANG NH GROWTH IN STATURE IN FRAGILE-X FAMILIES - A MIXED LONGITUDINAL-STUDY | 12 | 14 |
| 1297 | 14 | 21 | 1297 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):426-430 MCCONKIEROSELL A; ROBINSON H; WAKE S; STALEY LW; HELLER K; CRONISTER A DISSEMINATION OF GENETIC RISK INFORMATION TO RELATIVES IN THE FRAGILE-X SYNDROME - GUIDELINES FOR GENETIC COUNSELORS | 6 | 7 |
| 1298 | 1 | 9 | 1298 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):526-526 SCHIANO CM; DEMB HB; BROWN WT LACK OF SIGNIFICANT ASSOCIATION BETWEEN SPINA-BIFIDA AND THE FRAGILE-X SYNDROME | 0 | 0 |
| 1299 | 9 | 28 | 1299 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(1):39-43 SPINELLI M; ROCHA ACD; GIACHETI CM; RICHIERICOSTA A WORD-FINDING DIFFICULTIES, VERBAL PARAPHASIAS, AND VERBAL DYSPRAXIA IN 10 INDIVIDUALS WITH FRAGILE-X-SYNDROME | 5 | 5 |
| 1300 | 18 | 19 | 1300 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(4):302-306 MUELLER OT; HARTSFIELD JK; AMAR MJA; GALLARDO LA; KOUSSEFF BG FRAGILE-X SYNDROME - DISCORDANT LEVELS OF CGG REPEAT MOSAICISM IN 2 BROTHERS | 2 | 5 |
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