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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by year, source, volume, issue, page.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1201 | 15 | 21 | 1201 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):466-470 HOFSTEE Y; ARINAMI T; HAMAGUCHI H COMPARISON BETWEEN THE CYTOGENETIC TEST FOR FRAGILE-X AND THE MOLECULAR ANALYSIS OF THE FMR-1 GENE IN JAPANESE MENTALLY-RETARDED INDIVIDUALS | 15 | 20 |
| 1202 | 11 | 13 | 1202 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):471-473 HALLEY D; VANDENOUWELAND A; DEELEN W; VERMA I; OOSTRA B STRATEGY FOR RELIABLE PRENATAL DETECTION OF NORMAL-MALE CARRIERS OF THE FRAGILE-X-SYNDROME | 3 | 4 |
| 1203 | 27 | 37 | 1203 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):474-481 HAGERMAN RJ; WILSON P; STALEY LW; LANG KA; FAN T; et al. EVALUATION OF SCHOOL-CHILDREN AT HIGH-RISK FOR FRAGILE-X-SYNDROME UTILIZING BUCCAL CELL FMR-1 TESTING | 17 | 36 |
| 1204 | 16 | 21 | 1204 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):482-485 VANDENOUWELAND AMW; DEVRIES BBA; BAKKER PLG; DEELEN WH; DEGRAAFF E; et al. DNA DIAGNOSIS OF THE FRAGILE-X-SYNDROME IN A SERIES OF 236 MENTALLY-RETARDED SUBJECTS AND EVIDENCE FOR A REVERSAL OF MUTATION IN THE FMR-1 GENE | 29 | 35 |
| 1205 | 8 | 10 | 1205 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):486-489 VONKOSKULL H; GAHMBERG N; SALONEN R; SALO A; PEIPPO M FRAXA LOCUS IN FRAGILE-X DIAGNOSIS - FAMILY STUDIES, PRENATAL-DIAGNOSIS, AND DIAGNOSIS OF SPORADIC CASES OF MENTAL-RETARDATION | 8 | 8 |
| 1206 | 17 | 18 | 1206 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):490-496 MADDALENA A; HICKS BD; SPENCE WC; LEVINSON G; HOWARDPEEBLES PN PRENATAL-DIAGNOSIS IN KNOWN FRAGILE-X CARRIERS | 7 | 12 |
| 1207 | 12 | 13 | 1207 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):497-500 SMITS A; SMEETS D; HAMEL B; DREESEN J; DEHAAN A; et al. PREDICTION OF MENTAL STATUS IN CARRIERS OF THE FRAGILE-X MUTATION USING CGG REPEAT LENGTH | 13 | 16 |
| 1208 | 11 | 13 | 1208 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):501-502 KAPLAN G; KUNG M; MCCLURE M; CRONISTER A DIRECT MUTATION ANALYSIS OF 495 PATIENTS FOR FRAGILE-X CARRIER STATUS PROBAND DIAGNOSIS | 4 | 6 |
| 1209 | 16 | 17 | 1209 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):509-512 NOLIN SL; GLICKSMAN A; HOUCK GE; BROWN WT; DOBKIN CS MOSAICISM IN FRAGILE-X AFFECTED MALES | 39 | 41 |
| 1210 | 9 | 21 | 1210 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):513-516 DEELEN W; BAKKER C; HALLEY DJJ; OOSTRA BA CONSERVATION OF CGG REGION IN FMR1 GENE IN MAMMALS | 11 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1211 | 18 | 33 | 1211 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):517-521 CHIURAZZI P; KOZAK L; NERI G UNSTABLE TRIPLETS AND THEIR MUTATIONAL MECHANISM - SIZE-REDUCTION OF THE CGG REPEAT VS GERMLINE MOSAICISM IN THE FRAGILE-X-SYNDROME | 9 | 15 |
| 1212 | 4 | 11 | 1212 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):522-526 CHONG SS; EICHLER EE; NELSON DL; HUGHES MR ROBUST AMPLIFICATION AND ETHIDIUM-VISIBLE DETECTION OF THE FRAGILE-X-SYNDROME CGG REPEAT USING PFU POLYMERASE | 25 | 42 |
| 1213 | 12 | 21 | 1213 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):527-534 LEVINSON G; MADDALENA A; PALMER FT; HARTON GL; BICK DP; et al. IMPROVED SIZING OF FRAGILE-X CCG REPEATS BY NESTED POLYMERASE CHAIN-REACTION | 18 | 29 |
| 1214 | 0 | 0 | 1214 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):606-614 [Anon] ABSTRACTS FOR THE 6TH INTERNATIONAL WORKSHOP ON FRAGILE-X-SYNDROME AND X-LINKED MENTAL-RETARDATION | 0 | 0 |
| 1215 | 14 | 17 | 1215 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):370-373 PUISSANT H; MALINGE MC; LARGETPIET A; MARTIN D; CHAUVEAU P; et al. MOLECULAR ANALYSIS OF 53 FRAGILE-X FAMILIES WITH THE PROBE-STB12.3 | 1 | 2 |
| 1216 | 1 | 2 | 1216 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):380-381 PARK V; HOWARDPEEBLES P; SHERMAN S; TAYLOR A; WULFSBERG E POLICY STATEMENT - AMERICAN-COLLEGE-OF-MEDICAL-GENETICS - FRAGILE-X-SYNDROME - DIAGNOSTIC AND CARRIER TESTING | 17 | 28 |
| 1217 | 0 | 3 | 1217 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):382-382 HOWARDPEEBLES PN; MADDALENA A; SPENCE WC; LEVINSON G; FALLON L; et al. FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 5 | 9 |
| 1218 | 9 | 28 | 1218 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 54(2):141-143 CRADDOCK N; DANIELS J; MCGUFFIN P; OWEN M VARIATION AT THE FRAGILE X-LOCUS DOES NOT INFLUENCE SUSCEPTIBILITY TO BIPOLAR DISORDER | 1 | 6 |
| 1219 | 13 | 28 | 1219 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 54(4):378-383 THOMPSON NM; GULLEY ML; ROGENESS GA; CLAYTON RJ; JOHNSON C; et al. NEUROBEHAVIORAL CHARACTERISTICS OF CGG AMPLIFICATION STATUS IN FRAGILE-X FEMALES | 20 | 28 |
| 1220 | 16 | 33 | 1220 1994 AMERICAN JOURNAL ON MENTAL RETARDATION 98(4):455-462 KERBY DS; DAWSON BL AUTISTIC FEATURES, PERSONALITY, AND ADAPTIVE-BEHAVIOR IN MALES WITH THE FRAGILE-X SYNDROME AND NO AUTISM | 14 | 23 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1221 | 19 | 41 | 1221 1994 AMERICAN JOURNAL ON MENTAL RETARDATION 98(5):567-579 LACHIEWICZ AM; SPIRIDIGLIOZZI GA; GULLION CM; RANSFORD SN; RAO K ABERRANT BEHAVIORS OF YOUNG BOYS WITH FRAGILE X-SYNDROME | 28 | 33 |
| 1222 | 0 | 0 | 1222 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 |
| 1223 | 10 | 11 | 1223 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 |
| 1224 | 14 | 28 | 1224 1994 BRITISH JOURNAL OF CLINICAL PRACTICE 48(1):42-44 PATEL BD THE FRAGILE-X SYNDROME | 1 | 1 |
| 1225 | 0 | 0 | 1225 1994 CANADIAN FAMILY PHYSICIAN 40:290-295 WIEBE E; WIEBE A FRAGILE-X SYNDROME | 0 | 1 |
| 1226 | 1 | 16 | 1226 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 |
| 1227 | 16 | 39 | 1227 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 | 74 | 266 |
| 1228 | 21 | 53 | 1228 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 | 101 | 244 |
| 1229 | 23 | 52 | 1229 1994 CELL 78(1):23-33 BAKKER CE; VERHEIJ C; WILLEMSEN R; VANDERHELM R; OERLEMANS F; et al. FMR1 KNOCKOUT MICE - A MODEL TO STUDY FRAGILE-X MENTAL-RETARDATION | 96 | 163 |
| 1230 | 10 | 23 | 1230 1994 CLINICAL GENETICS 45(4):175-180 SCHRANDERSTUMPEL C; GERVER WJ; MEYER H; ENGELEN J; MULDER H; et al. PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X SYNDROME | 4 | 17 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1231 | 6 | 7 | 1231 1994 CLINICAL GENETICS 45(4):186-189 LOPEZPAJARES I; DELICADO A; PASCUALCASTROVIEJO I; LOPEZMARTIN V; MORENO F; et al. FRAGILE-X SYNDROME WITH EXTRA MICROCHROMOSOME | 0 | 1 |
| 1232 | 19 | 64 | 1232 1994 DEVELOPMENTAL BRAIN DYSFUNCTION 7(2-3):155-164 HAGERMAN RJ; FULTON MJ; LEAMAN A; RIDDLE J; HAGERMAN K; et al. A SURVEY OF FLUOXETINE THERAPY IN FRAGILE-X SYNDROME | 17 | 19 |
| 1233 | 58 | 91 | 1233 1994 EUROPEAN JOURNAL OF CLINICAL INVESTIGATION 24(1):1-10 ROUSSEAU F THE FRAGILE-X SYNDROME - IMPLICATIONS OF MOLECULAR-GENETICS FOR THE CLINICAL SYNDROME | 8 | 11 |
| 1234 | 0 | 19 | 1234 1994 GENES CHROMOSOMES & CANCER 9(2):141-144 RIGGINS GJ; SHERMAN SL; PHILLIPS CN; STOCK W; WESTBROOK CA; et al. CGG-REPEAT POLYMORPHISM OF THE BCR GENE RULES OUT PREDISPOSING ALLELES LEADING TO THE PHILADELPHIA-CHROMOSOME | 1 | 8 |
| 1235 | 5 | 30 | 1235 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 |
| 1236 | 4 | 6 | 1236 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 |
| 1237 | 19 | 28 | 1237 1994 HUMAN GENETICS 93(2):143-147 VAISANEN ML; KAHKONEN M; LEISTI J DIAGNOSIS OF FRAGILE-X SYNDROME BY DIRECT MUTATION ANALYSIS | 10 | 12 |
| 1238 | 21 | 34 | 1238 1994 HUMAN GENETICS 94(4):395-400 MILA M; KRUYER H; GLOVER G; SANCHEZ A; CARBONELL P; et al. MOLECULAR ANALYSIS OF THE (CGG)(N) EXPANSION IN THE FMR-1 GENE IN 59 SPANISH FRAGILE-X SYNDROME FAMILIES | 15 | 16 |
| 1239 | 13 | 19 | 1239 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 | 15 | 20 |
| 1240 | 18 | 25 | 1240 1994 HUMAN GENETICS 94(5):523-526 VITS L; DEBOULLE K; REYNIERS E; HANDIG I; DARBY JK; et al. APPARENT REGRESSION OF THE CGG REPEAT IN FMR1 TO AN ALLELE OF NORMAL SIZE | 16 | 20 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1241 | 23 | 31 | 1241 1994 HUMAN MOLECULAR GENETICS 3(3):393-398 REISS AL; KAZAZIAN HH; KREBS CM; MCAUGHAN A; BOEHM CD; et al. FREQUENCY AND STABILITY OF THE FRAGILE-X PREMUTATION | 34 | 61 |
| 1242 | 20 | 28 | 1242 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 | 37 | 58 |
| 1243 | 1 | 3 | 1243 1994 HUMAN MOLECULAR GENETICS 3(3):521-521 JOKINEN E; SAKAI J; YAMAMOTO T; HOBBS HH CGG TRIPLE REPEAT POLYMORPHISM IN VLDL RECEPTOR (VLDL-R) GENE | 0 | 16 |
| 1244 | 21 | 33 | 1244 1994 HUMAN MOLECULAR GENETICS 3(4):615-620 MEIJER H; DEGRAAFF E; MERCKX DML; JONGBLOED RJE; DEDIESMULDERS CEM; et al. A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1 GENE CAUSES THE CLINICAL PHENOTYPE OF THE FRAGILE X SYNDROME | 50 | 78 |
| 1245 | 18 | 29 | 1245 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 | 64 | 115 |
| 1246 | 27 | 46 | 1246 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 | 56 | 108 |
| 1247 | 7 | 18 | 1247 1994 INTELLIGENCE 19(1):45-50 DANIELS JK; OWEN MJ; MCGUFFIN P; THOMPSON L; DETTERMAN DK; et al. IQ AND VARIATION IN THE NUMBER OF FRAGILE-X CGG REPEATS - NO ASSOCIATION IN A NORMAL SAMPLE | 2 | 9 |
| 1248 | 1 | 5 | 1248 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 |
| 1249 | 1 | 1 | 1249 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(1):28-28 BROWN WT; HOUCK GE; JEZIOROWSKA A; LEVINSON FN; DING X; et al. RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST (VOL 270, PG 1569, 1993) | 1 | 1 |
| 1250 | 30 | 48 | 1250 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):507-514 TAYLOR AK; SAFANDA JF; FALL MZ; QUINCE C; LANG KA; et al. MOLECULAR PREDICTORS OF COGNITIVE INVOLVEMENT IN FEMALE CARRIERS OF FRAGILE-X SYNDROME | 80 | 92 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1251 | 42 | 81 | 1251 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):536-542 WARREN ST; NELSON DL ADVANCES IN MOLECULAR ANALYSIS OF FRAGILE-X SYNDROME | 74 | 129 |
| 1252 | 13 | 16 | 1252 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):552-553 CASKEY CT FRAGILE-X SYNDROME - IMPROVING UNDERSTANDING AND DIAGNOSIS | 2 | 2 |
| 1253 | 20 | 24 | 1253 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 |
| 1254 | 10 | 23 | 1254 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 |
| 1255 | 0 | 0 | 1255 1994 JOURNAL OF CELLULAR BIOCHEMISTRY :184-184 WARREN ST OVERVIEW AND UPDATE ON FMR1 AND FRAGILE-X SYNDROME | 0 | 0 |
| 1256 | 9 | 20 | 1256 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 |
| 1257 | 16 | 27 | 1257 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 |
| 1258 | 3 | 8 | 1258 1994 JOURNAL OF MEDICAL GENETICS 31(1):76-78 TEJADA MI; MORNET E; TIZZANO E; MOLINA M; BAIGET M; et al. IDENTIFICATION BY MOLECULAR DIAGNOSIS OF MOSAIC TURNERS-SYNDROME IN AN OBLIGATE CARRIER FEMALE FOR FRAGILE-X SYNDROME | 4 | 8 |
| 1259 | 0 | 0 | 1259 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 |
| 1260 | 0 | 0 | 1260 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1261 | 0 | 0 | 1261 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 |
| 1262 | 1 | 3 | 1262 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 |
| 1263 | 1 | 2 | 1263 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 |
| 1264 | 6 | 12 | 1264 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 |
| 1265 | 2 | 44 | 1265 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 | 12 | 55 |
| 1266 | 18 | 33 | 1266 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 | 21 | 36 |
| 1267 | 11 | 37 | 1267 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 | 25 | 33 |
| 1268 | 15 | 18 | 1268 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; et al. FRAGILE-X SYNDROME IN A NORMAL IQ MALE WITH LEARNING AND EMOTIONAL-PROBLEMS | 18 | 22 |
| 1269 | 1 | 6 | 1269 1994 KLINISCHE PADIATRIE 206(5):410-411 FEHLOW P; MIOSGE W; WALTHER F ASSOCIATION OF SAETHRE-CHOTZEN-SYNDROME AND FRAGILE-X-SYNDROME | 0 | 0 |
| 1270 | 2 | 5 | 1270 1994 LANCET 344(8935):1500-1500 TURNER G; ROBINSON H; WAKE S; MARTIN N DIZYGOUS TWINNING AND PREMATURE MENOPAUSE IN FRAGILE-X SYNDROME | 33 | 52 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1271 | 2 | 2 | 1271 1994 MENTAL RETARDATION 32(2):156-156 SPITZ HH FRAGILE-X SYNDROME IS NOT THE 2ND LEADING CAUSE OF MENTAL-RETARDATION | 0 | 1 |
| 1272 | 4 | 8 | 1272 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 |
| 1273 | 8 | 10 | 1273 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 |
| 1274 | 23 | 41 | 1274 1994 NATURE GENETICS 8(1):88-94 EICHLER EE; HOLDEN JJA; POPOVICH BW; REISS AL; SNOW K; et al. LENGTH OF UNINTERRUPTED CGG REPEATS DETERMINES INSTABILITY IN THE FMR1 GENE | 92 | 243 |
| 1275 | 0 | 0 | 1275 1994 NEUROLOGY 44(4):A400-A400 GUERREIRO M; MOURARIBEIRO MVL; CAMARGO EE; KATO M; MENEZES JR; et al. NEUROBIOLOGY OF FRAGILE-X-SYNDROME (FXS) | 0 | 0 |
| 1276 | 22 | 61 | 1276 1994 NEUROLOGY 44(7):1317-1324 REISS AL; LEE J; FREUND L NEUROANATOMY OF FRAGILE-X SYNDROME - THE TEMPORAL-LOBE | 54 | 89 |
| 1277 | 7 | 41 | 1277 1994 NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY 24(6):413-426 FERRI R; MUSUMECI SA; ELIA M; DELGRACCO S; SCUDERI C; et al. BIT-MAPPED SOMATOSENSORY-EVOKED POTENTIALS IN THE FRAGILE-X SYNDROME | 7 | 15 |
| 1278 | 3 | 26 | 1278 1994 NUCLEIC ACIDS RESEARCH 22(9):1735-1740 HAN J; HSU CC; ZHU Z; LONGSHORE JW; FINLEY WH OVER-REPRESENTATION OF THE DISEASE-ASSOCIATED (CAG) AND (CGG) REPEATS IN THE HUMAN GENOME | 2 | 25 |
| 1279 | 0 | 0 | 1279 1994 PEDIATRIC RESEARCH 35(4):A23-A23 LACHIEWICZ AM; DAWSON DV AUTISTIC BEHAVIORS OF YOUNG GIRLS WITH FRAGILE X-SYNDROME | 1 | 1 |
| 1280 | 14 | 31 | 1280 1994 PEDIATRICS 93(6):992-995 LACHIEWICZ AM; DAWSON DV DO YOUNG BOYS WITH FRAGILE-X-SYNDROME HAVE MACROORCHIDISM | 13 | 17 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1281 | 16 | 21 | 1281 1994 PRENATAL DIAGNOSIS 14(6):469-474 STRAIN L; PORTEOUS MEM; GOSDEN CM; ELLIS PM; NEILSON JP; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION | 3 | 4 |
| 1282 | 10 | 30 | 1282 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 | 39 | 148 |
| 1283 | 2 | 11 | 1283 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 |
| 1284 | 0 | 0 | 1284 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 |
| 1285 | 20 | 37 | 1285 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1042-1051 QUAN F; ZONANA J; GUNTER K; PETERSON KL; MAGENIS RE; et al. AN ATYPICAL CASE OF FRAGILE-X SYNDROME CAUSED BY A DELETION THAT INCLUDES THE FMRI GENE | 19 | 30 |
| 1286 | 19 | 65 | 1286 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1147-1155 FISCH GS; SNOW K; THIBODEAU SN; CHALIFAUX M; HOLDEN JJA; et al. THE FRAGILE-X PREMUTATION IN CARRIERS AND ITS EFFECT ON MUTATION SIZE IN OFFSPRING | 28 | 35 |
| 1287 | 21 | 51 | 1287 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 | 54 | 82 |
| 1288 | 36 | 54 | 1288 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(3):609-618 DEGRAAFF E; WILLEMSEN R; ZHONG N; DEDIESMULDERS CEM; BROWN WT; et al. INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF THE FMR1 PROTEIN IN A MALE FRAGILE-X PATIENT WITH A LUNG-TUMOR | 26 | 32 |
| 1289 | 0 | 0 | 1289 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 |
| 1290 | 0 | 0 | 1290 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 |
| 1291 | 0 | 0 | 1291 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):152-152 HUGHES MR; HADDAD BR; SUBRAMANIAN S; NASONKIN I; COTA J; et al. 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 |
| 1292 | 0 | 0 | 1292 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):153-153 BLACK SH; LEVINSON G; HARTON GL; PALMER FT; SISSON ME; et al. PREIMPLANTATION GENETIC TESTING (PGT) FOR FRAGILE-X (FRAX) | 2 | 3 |
| 1293 | 0 | 0 | 1293 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 |
| 1294 | 0 | 0 | 1294 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):211-211 NELSON DL; KUNST CB; LUGENBEEL KA; RYDER OA; WARREN ST; et al. EVOLUTION OF THE CRYPTIC FMR1 CGG REPEAT | 0 | 0 |
| 1295 | 0 | 0 | 1295 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 |
| 1296 | 0 | 0 | 1296 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):585-585 WRIGHTTALAMANTE C; CHEEMA A; RIDDLE JE; LUCKEY D; TAYLOR A; et al. A CONTROLLED-STUDY OF LONGITUDINAL IQ CHANGES IN FEMALES AND MALES WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1297 | 0 | 0 | 1297 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):655-655 JENKINS EC; DOBKIN CS; DING X; LI SY; HOUCK GE; et al. THRESHOLD CGG REPEAT SIZE FOR FRAGILE SITE EXPRESSION WITHOUT METHYLATION IDENTIFIED IN LYMPHOCYTE, LYMPHOBLASTOID AND CLONAL LYMPHOBLASTOID CULTURES FROM AN FMR1 UNMETHYLATED MOSAIC FULL MUTATION INDIVIDUAL | 0 | 0 |
| 1298 | 0 | 0 | 1298 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 |
| 1299 | 0 | 0 | 1299 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):692-692 RANCHINO B; TARAVATH A; KALICHMAN M; BURTON BB; MCCORQUODALE MM; et al. SELECTION AGAINST A MARKER CHROMOSOME IN FRAGILE-X-STRESSED CULTURES | 0 | 0 |
| 1300 | 0 | 0 | 1300 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):869-869 WINKELER KA; WARREN ST VARIATIONS IN THE LENGTH OF THE CGG-REPEAT OF FMR-1 AFFECT GENE-EXPRESSION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1301 | 1 | 1 | 1301 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 |
| 1302 | 0 | 0 | 1302 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):913-913 BROWN WT; ZHONG N; KAJANOJA E; SMITS B; CURLEY D; et al. FRAGILE-X FOUNDER CHROMOSOME EFFECTS AND NEW MUTATIONS | 0 | 0 |
| 1303 | 0 | 0 | 1303 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):919-919 CHIURAZZI P; KOZAK L; GENUARDI M; GIOVANNUCCIUZIELLI ML; BUSSANI C; et al. FRAGILE-X SYNDROME - ROUNDER CHROMOSOMES IN ITALY | 0 | 0 |
| 1304 | 0 | 0 | 1304 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):965-965 NOLIN SL; GLICKSMAN A; LEWIS FA; YE LL; HOUCK GE; et al. EVIDENCE FOR A FAMILIAL FACTOR INVOLVED IN CGG REPEAT EXPANSION IN FRAGILE-X SYNDROME | 0 | 0 |
| 1305 | 0 | 0 | 1305 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1088-1088 CURLEY D; ZHONG N; WANG DW; JU W; DOBKIN C; et al. NEW INTRAGENIC ALU POLYMORPHISMS IN THE FRAGILE-X GENE | 0 | 0 |
| 1306 | 0 | 0 | 1306 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1218-1218 FALIKBORENSTEIN TC; YALON M; SHACHAK L; DAR C; BOROCHOWITZ Z; et al. LONG UNINTERRUPTED CGG REPEATS WITHIN THE FMR1 GENE - POSSIBLE MECHANISM FOR THE PREVALENCE OF THE FRAGILE-X SYNDROME AMONG TUNISIAN JEWS | 0 | 0 |
| 1307 | 0 | 0 | 1307 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1273-1273 MILA M; CASTELLVIBEL S; BARCELO A; SANCHEZ A; JIMENEZ D; et al. MUTATIONS IN THE CPG ISLAND OF THE FMR1 GENE - ARE THEY RESPONSIBLE FOR FRAGILE-X SYNDROME | 0 | 0 |
| 1308 | 0 | 0 | 1308 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 |
| 1309 | 0 | 0 | 1309 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1344-1344 WILLEMSEN R; BAKKER C; MANDEL JL; DEVRIES B; DEVYS D; et al. RAPID SCREENING-TEST FOR FRAGILE-X SYNDROME | 0 | 0 |
| 1310 | 0 | 0 | 1310 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1359-1359 BAKKER C; DEGRAAFF E; ZHONG N; WILLEMSEN R; OOSTRA B INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF FMR1 PROTEIN IN A MALE-PATIENT WITH A LUNG-TUMOR | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1311 | 0 | 0 | 1311 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 |
| 1312 | 0 | 0 | 1312 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1407-1407 JOHNSON JP; CURRY C; MICEK M; LOUIE E; ABRAMS L; et al. TRANSMISSION OF STABLE AND UNSTABLE PREMUTATIONS FROM GREAT-GRANDMOTHER AND GREAT-GRANDFATHER RESPECTIVELY - LESSONS FOR GENETIC-COUNSELING IN FRAGILE-X SYNDROME FAMILIES | 0 | 0 |
| 1313 | 0 | 0 | 1313 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 |
| 1314 | 0 | 0 | 1314 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 |
| 1315 | 0 | 0 | 1315 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1705-1705 DEVRIES BBA; VANDENOUWELAND AMW; MOHKAMSING S; HALLEY DJJ; TIBBEN A; et al. ACCEPTANCE OF SCREENING FOR THE FRAGILE-X SYNDROME AMONG 1878 MENTALLY-RETARDED INDIVIDUALS IN INSTITUTES AND SPECIAL SCHOOLS IN THE NETHERLANDS | 0 | 0 |
| 1316 | 0 | 0 | 1316 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1838-1838 EIGEL A; ZYGULSKA M; DOLSCHEID T; BOGDANOVA N; DWORNICZAK B; et al. FRAGILE-X PREMUTATION FREQUENCY IN NORTHERN THAILAND | 0 | 0 |
| 1317 | 1 | 1 | 1317 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 |
| 1318 | 0 | 0 | 1318 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 |
| 1319 | 0 | 0 | 1319 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 |
| 1320 | 0 | 0 | 1320 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1947-1947 BROWN CA; BRASINGTON CK; GRASS FS PATERNAL TRANSMISSION OF A FULL MUTATION IN THE FMR1 GENE - IDENTIFICATION OF PATERNAL CGG REPEAT SHES IN MULTIPLE TISSUES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1321 | 12 | 21 | 1321 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 | 9 | 14 |
| 1322 | 34 | 42 | 1322 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 | 86 | 114 |
| 1323 | 21 | 27 | 1323 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 | 8 | 13 |
| 1324 | 27 | 42 | 1324 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 | 18 | 20 |
| 1325 | 11 | 13 | 1325 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 55(3):384-386 PRIOR TW; PAPP AC; SNYDER PJ; SEDRA MS; GUIDA M; et al. GERMLINE MOSAICISM AT THE FRAGILE-X LOCUS | 2 | 7 |
| 1326 | 2 | 5 | 1326 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 57(3):508-509 LAXOVA R FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 2 | 3 |
| 1327 | 16 | 33 | 1327 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 |
| 1328 | 14 | 21 | 1328 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):426-430 MCCONKIEROSELL A; ROBINSON H; WAKE S; STALEY LW; HELLER K; et al. DISSEMINATION OF GENETIC RISK INFORMATION TO RELATIVES IN THE FRAGILE-X SYNDROME - GUIDELINES FOR GENETIC COUNSELORS | 7 | 8 |
| 1329 | 1 | 9 | 1329 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 |
| 1330 | 9 | 28 | 1330 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 | 7 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1331 | 18 | 19 | 1331 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 |
| 1332 | 28 | 92 | 1332 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(6):480-493 Schapiro MB; Murphy DGM; Hagerman RJ; Azari NP; Alexander GE; et al. Adult fragile X syndrome: Neuropsychology, brain anatomy, and metabolism | 21 | 31 |
| 1333 | 12 | 24 | 1333 1995 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 172(4):1236-1239 RYYNANEN M; KIRKINEN P; MANNERMAA A; SAARIKOSKI S CARRIER DIAGNOSIS OF THE FRAGILE-X SYNDROME - A CHALLENGE IN ANTENATAL CLINICS | 6 | 8 |
| 1334 | 0 | 0 | 1334 1995 ANNALS OF NEUROLOGY 38(3):499-499 BERRYKRAVIS E; CIURLIONIS R OVEREXPRESSION OF FRAGILE-X GENE (FMR-1) TRANSCRIPTS IN NEURAL CELLS RESULTS IN INCREASED LEVELS OF CYCLIC ADENOSINE-MONOPHOSPHATE PRODUCTION | 0 | 0 |
| 1335 | 71 | 125 | 1335 1995 ANNUAL REVIEW OF NEUROSCIENCE 18:77-99 WARREN ST; ASHLEY CT TRIPLET REPEAT EXPANSION MUTATIONS - THE EXAMPLE OF FRAGILE-X SYNDROME | 26 | 58 |
| 1336 | 27 | 43 | 1336 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):3-5 TURK J FRAGILE-X SYNDROME | 2 | 4 |
| 1337 | 16 | 30 | 1337 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):33-37 SLANEY SF; WILKIE AOM; HIRST MC; CHARLTON R; MCKINLEY M; et al. DNA TESTING FOR FRAGILE-X SYNDROME IN SCHOOLS FOR LEARNING-DIFFICULTIES | 13 | 21 |
| 1338 | 2 | 5 | 1338 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(6):544-544 TURK J TREATMENT OF FRAGILE-X SYNDROME | 0 | 0 |
| 1339 | 11 | 19 | 1339 1995 ARCHIVES OF MEDICAL RESEARCH 26:S77-S83 DiazGallardo MY; BarrosNunez P; Diaz CA; Hernandez A; GomezEspinel I; et al. Molecular characterization of the fragile-X syndrome in the Mexican population | 2 | 4 |
| 1340 | 3 | 42 | 1340 1995 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 217(3):1015-1025 Xing GQ; Zhang LX; Zhang L; Heynen T; Yoshikawa T; et al. Rat PPAR delta contains a CGG triplet repeat and is prominently expressed in the thalamic nuclei | 0 | 54 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1341 | 2 | 32 | 1341 1995 BIOCHEMISTRY 34(39):12803-12811 MITAS M; YU A; DILL J; HAWORTH IS THE TRINUCLEOTIDE REPEAT SEQUENCE D(CGG)(15) FORMS A HEAT-STABLE HAIRPIN CONTAINING G(SYN)CENTER-DOT-G(ANTI) BASE-PAIRS | 15 | 63 |
| 1342 | 40 | 112 | 1342 1995 BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE 1271(2-3):293-303 FLANNERY AV; HIRST MC; KNIGHT SJL; RITCHIE RJ; DAVIES KE THE FRAGILE-X SYNDROME | 2 | 5 |
| 1343 | 0 | 0 | 1343 1995 BIOLOGICAL PSYCHIATRY 37(9):629-629 REISS AL FRAGILE-X SYNDROME | 0 | 0 |
| 1344 | 0 | 24 | 1344 1995 BIOPHYSICAL JOURNAL 69(2):553-558 RAMAKRISHNAN B; SUNDARALINGAM M CRYSTAL-STRUCTURE OF THE A-DNA DECAMER D(CCIGGCCM(5)CGG) AT 1.6-ANGSTROM SHOWING THE UNEXPECTED WOBBLE I-CENTER-DOT-M(5)C BASE-PAIR | 0 | 7 |
| 1345 | 0 | 30 | 1345 1995 BIOSPECTROSCOPY 1(4):235-245 CARMONA P; MOLINA M; LASAGABASTER A; ESCOBAR R DETERMINATION OF THE HYDROGEN-BONDED STRUCTURE OF CGG TRIMERS IN CHLOROFORM SOLUTION BY VIBRATIONAL SPECTROSCOPY | 0 | 2 |
| 1346 | 2 | 6 | 1346 1995 BONE MARROW TRANSPLANTATION 16(4):625-626 MORTON J; ARNOLD L; FLETCHER B; MCCARTHY C; ROWELL J; et al. ALLOGENEIC BMT FROM A DONOR WITH FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR EVALUATION | 0 | 0 |
| 1347 | 26 | 39 | 1347 1995 BRAIN & DEVELOPMENT 17(5):317-321 NANBA E; KOHNO Y; MATSUDA A; YANO M; SATO C; et al. NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED JAPANESE MALES | 8 | 17 |
| 1348 | 4 | 5 | 1348 1995 BRAIN & DEVELOPMENT 17(5):322-322 NAKAHORI Y THE INCIDENCE OF THE FRAGILE-X SYNDROME IN JAPANESE - COMMENTARY ON NANBAS PAPER | 0 | 0 |
| 1349 | 4 | 7 | 1349 1995 BRAIN & DEVELOPMENT 17(5):323-323 KONDO I NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN JAPANESE MENTALLY-RETARDED MALES - COMMENT | 0 | 0 |
| 1350 | 0 | 0 | 1350 1995 BRAIN AND COGNITION 28(1):111-111 GRIGSBY J; KAYE K VARIABLE EXPRESSION OF DEVELOPMENTAL GERSTMANN SIGNS IN FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1351 | 0 | 0 | 1351 1995 BRAIN AND COGNITION 28(1):111-112 GRIGSBY J; KAYE K DISSOCIATIONS IN DEVELOPMENTAL DYSCALCULIA SECONDARY TO FRAGILE-X SYNDROME | 0 | 0 |
| 1352 | 0 | 1 | 1352 1995 BRITISH JOURNAL OF PSYCHIATRY 166:688-688 COOKE LB BEHAVIOR AND DEVELOPMENT IN FRAGILE-X SYNDROME - DYKENS,E | 0 | 0 |
| 1353 | 0 | 1 | 1353 1995 BRITISH MEDICAL JOURNAL 310(6973):148-148 CRAFT N STUDY SUPPORTS SCREENING FOR THE FRAGILE-X-SYNDROME | 2 | 3 |
| 1354 | 0 | 0 | 1354 1995 CLINICAL CHEMISTRY 41(11):30-30 RADU DN; CHIANG CS RAPID, NONRADIOACTIVE SOUTHERN BLOT METHOD FOR DETECTING FRAGILE-X MUTATIONS | 0 | 0 |
| 1355 | 45 | 78 | 1355 1995 CLINICS IN LABORATORY MEDICINE 15(4):859-& Brown WT Perspectives and molecular diagnosis of the fragile X syndrome | 2 | 2 |
| 1356 | 0 | 0 | 1356 1995 CYTOGENETICS AND CELL GENETICS 69(1-2):116-116 HOWARDPEEBLES PN IT IS TIME TO ABANDON THE CYTOGENETIC FRAGILE-X TEST | 0 | 0 |
| 1357 | 9 | 23 | 1357 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):167-184 Hagerman R; Staley L; Brown WT; Taylor A; Meadow K; et al. Conference summary: Fourth International Conference on Fragile X and X-linked Mental Retardation sponsored by the National Fragile X Foundation | 0 | 0 |
| 1358 | 0 | 0 | 1358 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):185-186 Nommensen D Report of the Executive Director of the National Fragile X Foundation | 0 | 0 |
| 1359 | 32 | 75 | 1359 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):187-198 Abrams MT; Reiss AL Quantitative brain imaging studies of fragile X syndrome | 2 | 3 |
| 1360 | 46 | 131 | 1360 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):199-217 Binstock TC Fragile X and the amygdala: Cognitive, interpersonal, emotional, and neuroendocrine considerations | 4 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1361 | 3 | 16 | 1361 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):218-222 Musumeci SA; Ferri R; Elia M; DalGracco S; Scuderi C; et al. Sleep neurophysiology in fragile X patients | 2 | 3 |
| 1362 | 10 | 22 | 1362 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):223-229 King RA; Hagerman R; Houghton M Ocular findings in fragile X syndrome | 1 | 1 |
| 1363 | 27 | 36 | 1363 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):230-241 Brun C; Obiols JE; Cheema A; OConnor R; Riddle J; et al. Longitudinal IQ changes in fragile X females | 1 | 1 |
| 1364 | 17 | 33 | 1364 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):242-251 Freund LS; Peebles CD; Aylward E; Reiss AL Preliminary report on cognitive and adaptive behaviors of preschool-aged males with fragile X | 17 | 22 |
| 1365 | 40 | 75 | 1365 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):252-269 Cohen IL Behavioral profiles of autistic and nonautistic fragile X males | 12 | 13 |
| 1366 | 15 | 38 | 1366 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):270-279 Belser RC; Sudhalter V Arousal difficulties in males with fragile X syndrome: A preliminary report | 21 | 26 |
| 1367 | 19 | 37 | 1367 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):280-292 Sobesky WE; Porter D; Pennington BF; Hagerman RJ Dimensions of shyness in fragile X females | 14 | 19 |
| 1368 | 26 | 41 | 1368 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):293-301 Jenkins EC; Houck GE; Ding XH; Li SY; StarkHouck SL; et al. An update on fragile X prenatal diagnosis: End of the cytogenetic testing era | 1 | 1 |
| 1369 | 18 | 26 | 1369 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):302-309 Holden JJA; Chalifoux M; Wing M; JulienInalsingh C; Scott E; et al. Distribution and frequency of FMR1 CGG repeat number in institutionalized developmentally disabled individuals | 0 | 2 |
| 1370 | 12 | 21 | 1370 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):319-326 Wake SA; Robinson H Assessment of counselling of normal males and normal transmitting male carriers identified in fragile X families | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1371 | 10 | 25 | 1371 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):327-335 Roy JC; Johnsen J; Breese K; Hagerman R Fragile X syndrome: What is the impact of diagnosis on families? | 3 | 6 |
| 1372 | 8 | 35 | 1372 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):336-344 Hagerman RJ; Riddle JE; Roberts LS; Breese K; Fulton M Survey of the efficacy of clonidine in fragile X syndrome | 12 | 12 |
| 1373 | 2 | 23 | 1373 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):345-352 Rattazzi MC Protein therapy in fragile X syndrome - A brief overview of principles, potentials and problems | 0 | 0 |
| 1374 | 0 | 7 | 1374 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):359-362 Lin JFH Introduction to fragile X syndrome for parents | 0 | 0 |
| 1375 | 0 | 0 | 1375 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):363-366 Glass L Females with fragile X: A parent's perspective | 0 | 0 |
| 1376 | 6 | 9 | 1376 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):370-379 Holden JJA Workshop for family and friends .1. The fragile X gene and its mutations | 0 | 0 |
| 1377 | 0 | 0 | 1377 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):390-395 McConkieRosell A; Robinson H; Wake S; Staley L; Heller K; et al. Educating extended family members about the inheritance of the fragile X syndrome | 0 | 1 |
| 1378 | 7 | 18 | 1378 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):396-404 Mazzocco MMM; Lachiewicz AM; Kovar CG; Freund LS; Baumgardner TL; et al. Psychological and emotional studies of the fragile X mutation - A workshop summary | 0 | 0 |
| 1379 | 7 | 8 | 1379 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):405-407 Holden JJA; Chalifoux M; Wing M; JulienInalsingh C; Lawson JS; et al. Distribution and frequency of FMR1 CGG repeat numbers in the general population | 6 | 13 |
| 1380 | 5 | 9 | 1380 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):408-410 HowardPeebles PN; Maddalena A; Black SH; Levinson G; Bick DP; et al. Fragile X screening in pediatric and obstetrical patients | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1381 | 0 | 0 | 1381 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):411-416 [Anon] 4th International Fragile X and X-Linked Mental Retardation Conference - Albuquerque, NM, USA, June 8-12, 1994 - Abstracts | 0 | 0 |
| 1382 | 13 | 16 | 1382 1995 DIAGNOSTIC MOLECULAR PATHOLOGY 4(3):158-161 NABER SP MOLECULAR DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| 1383 | 14 | 43 | 1383 1995 EMBO JOURNAL 14(11):2401-2408 SIOMI MC; SIOMI H; SAUER WH; SRINIVASAN S; NUSSBAUM RL; et al. FXR1, AN AUTOSOMAL HOMOLOG OF THE FRAGILE-X MENTAL-RETARDATION GENE | 62 | 102 |
| 1384 | 16 | 36 | 1384 1995 EMBO JOURNAL 14(21):5358-5366 ZHANG Y; OCONNOR JP; SIOMI MC; SRINIVASAN S; DUTRA A; et al. THE FRAGILE-X MENTAL-RETARDATION SYNDROME PROTEIN INTERACTS WITH NOVEL HOMOLOGS FXR1 AND FXR2 | 77 | 121 |
| 1385 | 0 | 0 | 1385 1995 EPILEPSIA 36:S1-S1 KLUGER G; BOHM I; LAUB MC; WALDENMEIER C; STUHRMANNSPANGENBERG M EEG IN CHILDREN WITH FRAGILE-X PREMUTATION | 0 | 0 |
| 1386 | 0 | 0 | 1386 1995 EPILEPSIA 36:S244-S244 SINGH R; SUTHERLAND G; MANSON J SEIZURES WITH EPILEPTOGENIC EEG PATTERN IN 2 SISTERS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1387 | 0 | 0 | 1387 1995 FASEB JOURNAL 9(6):A1324-A1324 MITAS M; YU A; DILL J; HAWORTH IS HAIRPIN PROPERTIES OF SINGLE-STRANDED-DNA CONTAINING G+C-RICH TRIPLET REPEATS - (CTG)(15) AND (CGG)(15) | 0 | 0 |
| 1388 | 0 | 0 | 1388 1995 FASEB JOURNAL 9(6):A1324-A1324 SMITH SS; LAAYOUN A; BAKER DJ; KHO MR RECOGNITION OF TELOMERE-LIKE STRUCTURES FROM THE HUMAN C-HA-RAS GENE AND THE TRINUCLEOTIDE REPEAT OF THE FMR-1 GENE OF FRAGILE-X BY HUMAN DNA METHYLTRANSFERASE | 0 | 0 |
| 1389 | 3 | 4 | 1389 1995 GENETIC COUNSELING 6(2):97-101 BORGHGRAEF M; SWILLEN A; VANDENBERGHE H; FRYNS JP FRAGILE-X BOYS - EVOLUTION OF THE MENTAL AGE IN CHILDHOOD - PRELIMINARY DATA ON 10 PREPUBERTAL BOYS | 0 | 0 |
| 1390 | 2 | 9 | 1390 1995 GENETIC COUNSELING 6(3):207-210 ALEMBIK Y; DOTT B; STOLL C RETT-LIKE SYNDROME IN FRAGILE-X SYNDROME | 1 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1391 | 1 | 4 | 1391 1995 GENETIC COUNSELING 6(4):293-296 FRYNS JP SCREENING FOR THE FRAGILE-X SYNDROME - THE NECESSITY OF INTERNATIONAL GUIDELINES FOR MOLECULAR-GENETICS PREDICTIVE TESTING IN GENERAL | 2 | 3 |
| 1392 | 12 | 26 | 1392 1995 GENETIC EPIDEMIOLOGY 12(3):279-290 HUGGINS RM; LOESCH DZ USE OF ROBUST STATISTICAL-METHODS TO DETERMINE THE EFFECT OF FRAGILE-X ON MEANS AND VARIANCE-COMPONENTS OF A QUANTITATIVE TRAIT | 1 | 2 |
| 1393 | 17 | 33 | 1393 1995 HUMAN GENETICS 96(3):323-329 DREESEN JCFM; GERAEDTS JPM; DUMOULIN JCM; EVERS JLH; PIETERS MHEC RS46(DXS548) GENOTYPING OF REPRODUCTIVE CELLS - APPROACHING PREIMPLANTATION TESTING OF THE FRAGILE-X SYNDROME | 2 | 7 |
| 1394 | 0 | 5 | 1394 1995 HUMAN GENETICS 96(3):369-370 LENCH NJ; THOMPSON J; MARKHAM AF; ROBINSON PA (CGG) TRINUCLEOTIDE REPEAT POLYMORPHISM IN THE 5'-REGION OF THE HHR6B GENE - THE HUMAN HOMOLOG OF THE YEAST DNA-REPAIR GENE RAD6 | 0 | 1 |
| 1395 | 20 | 28 | 1395 1995 HUMAN GENETICS 96(5):577-584 ELALEEM AA; BOHM I; TEMTAMY S; ELAWADY M; AWADALLA M; et al. DIRECT MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME IN A SAMPLE OF EGYPTIAN AND GERMAN PATIENTS USING NONRADIOACTIVE PCR AND SOUTHERN BLOT FOLLOWED BY CHEMILUMINESCENT DETECTION | 6 | 9 |
| 1396 | 26 | 49 | 1396 1995 HUMAN MOLECULAR GENETICS 4(1):45-49 DEGRAAFF E; ROUILLARD P; WILLEMS PJ; SMITS APT; ROUSSEAU F; et al. HOTSPOT FOR DELETIONS IN THE CGG REPEAT REGION OF FMR1 IN FRAGILE-X PATIENTS | 31 | 46 |
| 1397 | 18 | 31 | 1397 1995 HUMAN MOLECULAR GENETICS 4(9):1681-1684 QUAN F; GROMPE M; JAKOBS P; POPOVICH BW SPONTANEOUS DELETION IN THE FMR1 GENE IN A PATIENT WITH FRAGILE-X SYNDROME AND CHERUBISM | 9 | 14 |
| 1398 | 15 | 25 | 1398 1995 HUMAN MOLECULAR GENETICS 4(12):2199-2208 EICHLER EE; HAMMOND HA; MACPHERSON JN; WARD PA; NELSON DL POPULATION SURVEY OF THE HUMAN FMR1 CGG REPEAT SUBSTRUCTURE SUGGESTS BIASED POLARITY FOR THE LOSS OF AGG INTERRUPTIONS | 20 | 35 |
| 1399 | 8 | 11 | 1399 1995 ISRAEL JOURNAL OF MEDICAL SCIENCES 31(5):323-325 DAR H; SCHAAP T; BAITOR H; BOROCHOWITZ Z; GELMANKOHAN Z; et al. ETHNIC DISTRIBUTION OF THE FRAGILE-X SYNDROME IN ISRAEL - EVIDENCE OF FOUNDER CHROMOSOMES() | 1 | 1 |
| 1400 | 5 | 24 | 1400 1995 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 25(6):655-662 Lenti C; Peruzzi C; Bianchini E The association between autism and fragile X syndrome: A case report | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1401 | 1 | 22 | 1401 1995 JOURNAL OF BACTERIOLOGY 177(7):1915-1917 FUTO S; SETO Y; MITSUSE S; MORI Y; SUZUKI T; et al. MOLECULAR-CLONING OF A 46-KILODALTON SURFACE-ANTIGEN (P46) GENE FROM MYCOPLASMA-HYOPNEUMONIAE - DIRECT EVIDENCE OF CGG CODON USAGE FOR ARGININE | 0 | 9 |
| 1402 | 2 | 43 | 1402 1995 JOURNAL OF BIOLOGICAL CHEMISTRY 270(39):23090-23096 CHEN FM ACID-FACILITATED SUPRAMOLECULAR ASSEMBLY OF G-QUADRUPLEXES IN D(CGG)(4) | 10 | 37 |
| 1403 | 3 | 44 | 1403 1995 JOURNAL OF BIOLOGICAL CHEMISTRY 270(45):27014-27021 KANG SM; OHSHIMA K; SHIMIZU M; AMIRHAERI S; WELLS RD PAUSING OF DNA-SYNTHESIS IN-VITRO AT SPECIFIC LOCI IN CTG AND CGG TRIPLET REPEATS FROM HUMAN HEREDITARY-DISEASE GENES | 16 | 96 |
| 1404 | 15 | 46 | 1404 1995 JOURNAL OF BIOLOGICAL CHEMISTRY 270(48):28970-28977 NADEL Y; WEISMANSHOMER P; FRY M THE FRAGILE-X SYNDROME SINGLE-STRAND D(CGG)(N) NUCLEOTIDE REPEATS READILY FOLD BACK TO FORM UNIMOLECULAR HAIRPIN STRUCTURES | 17 | 50 |
| 1405 | 0 | 0 | 1405 1995 JOURNAL OF CELLULAR BIOCHEMISTRY :100-100 MCMURRAY CT; GACY AM; GOELLNER G HAIRPIN STABILITY DETERMINES THE THRESHOLD AND POTENTIAL FOR NUCLEOTIDE EXPANSION ASSOCIATED WITH HUMAN NEURODEGENERATIVE DISEASE | 0 | 0 |
| 1406 | 0 | 0 | 1406 1995 JOURNAL OF CELLULAR BIOCHEMISTRY :373-373 WILLEMS PJ; BAKKER CE; REYNIERS E; VERHEIJ C; DEBOULLE K; et al. A TRANSGENIC MOUSE MODEL FOR FRAGILE-X SYNDROME | 0 | 0 |
| 1407 | 0 | 1 | 1407 1995 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 36(4):707-707 TURK J BEHAVIOR AND DEVELOPMENT IN FRAGILE-X SYNDROME - DYKENS,EM, HODAPP,RM, LECKMAN,JF | 0 | 0 |
| 1408 | 23 | 37 | 1408 1995 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 17(4):518-528 HINTON VJ; HALPERIN JM; DOBKIN CS; DING XH; BROWN WT; et al. COGNITIVE AND MOLECULAR ASPECTS OF FRAGILE-X | 5 | 9 |
| 1409 | 2 | 14 | 1409 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 |
| 1410 | 15 | 26 | 1410 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:544-553 Butler MG; Pratesi R; VnencakJones CL Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1411 | 0 | 0 | 1411 1995 JOURNAL OF MEDICAL GENETICS 32(2):144-145 MORTON JE; RINDL PM; BULLOCK S; BUNDEY S; WEBB T FRAGILE-X SYNDROME IS LESS COMMON THAN PREVIOUSLY ESTIMATED | 2 | 2 |
| 1412 | 0 | 0 | 1412 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 WANG Q; GREEN EP; BOBROW M; MATHEW CG SCREENING FOR THE FRAGILE-X A-MUTATION AND E-MUTATION BY AUTOMATED FLUORESCENT ANALYSIS | 0 | 0 |
| 1413 | 0 | 0 | 1413 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 BULLOCK S; LINDLEY VH; STEVENSON K; COLE T MOLECULAR DNA TESTING OF A FAMILY MANIFESTING FRAGILE-X SYNDROME IN BOTH THE FRAX-A FULL MUTATION AND MOSAIC FORMS | 0 | 0 |
| 1414 | 0 | 0 | 1414 1995 JOURNAL OF MEDICAL GENETICS 32(2):154-154 BULLOCK S; FELIX CA; BUTTERWORTH MA; STEVENSON K; WILLIAMS D THE USE OF MOLECULAR DNA TESTING TO DISTINGUISH BETWEEN MUTATIONS AT THE FRAGILE-X A-SITES AND E-SITES | 0 | 0 |
| 1415 | 10 | 20 | 1415 1995 JOURNAL OF MEDICAL GENETICS 32(3):170-173 WANG Q; GREEN E; BOBROW M; MATHEW CG A RAPID, NONRADIOACTIVE SCREENING-TEST FOR FRAGILE-X MUTATIONS AT THE FRAXA AND FRAXE LOCI | 17 | 28 |
| 1416 | 17 | 27 | 1416 1995 JOURNAL OF MEDICAL GENETICS 32(3):236-239 MACPHERSON JN; CURTIS G; CROLLA JA; DENNIS N; MIGEON B; et al. UNUSUAL (CGG)(N) EXPANSION AND RECOMBINATION IN A FAMILY WITH FRAGILE-X AND DIGEORGE-SYNDROME | 5 | 11 |
| 1417 | 16 | 40 | 1417 1995 JOURNAL OF MEDICAL GENETICS 32(10):764-769 DEVRIES BBA; ROBINSON H; STOLTEDIJKSTRA I; GI CVTP; DIJKSTRA PF; et al. GENERAL OVERGROWTH IN THE FRAGILE-X SYNDROME - VARIABILITY IN THE PHENOTYPIC-EXPRESSION OF THE FMR1 GENE MUTATION | 6 | 16 |
| 1418 | 8 | 12 | 1418 1995 JOURNAL OF MEDICAL GENETICS 32(11):907-908 PINTADO E; DEDIEGO Y; HMADCHA A; CARRASCO M; SIERRA J; et al. INSTABILITY OF THE CGG REPEAT AT THE FRAXA LOCUS AND VARIABLE PHENOTYPIC-EXPRESSION IN A LARGE FRAGILE-X PEDIGREE | 2 | 9 |
| 1419 | 14 | 35 | 1419 1995 JOURNAL OF MEDICAL GENETICS 32(12):925-929 KIRCHGESSNER CU; WARREN ST; WILLARD HF X INACTIVATION OF THE FMR1 FRAGILE-X MENTAL-RETARDATION GENE | 5 | 13 |
| 1420 | 11 | 67 | 1420 1995 JOURNAL OF MOLECULAR BIOLOGY 254(4):638-656 KETTANI A; KUMAR RA; PATEL DJ SOLUTION STRUCTURE OF A DNA QUADRUPLEX CONTAINING THE FRAGILE-X SYNDROME TRIPLET REPEAT | 15 | 98 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1421 | 8 | 9 | 1421 1995 LANCET 345(8958):1147-1148 WILLEMSEN R; MOHKAMSING S; DEVRIES B; DEVYS D; VANDENOUWELAND A; et al. RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME | 81 | 101 |
| 1422 | 2 | 5 | 1422 1995 LANCET 346(8970):309-310 CONWAY GS; HETTIARACHCHI S; MURRAY A; JACOBS PA FRAGILE-X PREMUTATIONS IN FAMILIAL PREMATURE OVARIAN FAILURE | 21 | 43 |
| 1423 | 36 | 59 | 1423 1995 MEDICINA-BUENOS AIRES 55(5):457-466 BANARES VG UPDATING THE FRAGILE-X SYNDROME | 0 | 0 |
| 1424 | 0 | 0 | 1424 1995 MOLECULAR BIOLOGY OF THE CELL 6:1801-1801 TANEJA KL; NELSON D; SINGER RH SPATIAL-DISTRIBUTION OF CGG REPEAT SEQUENCES IN NUCLEI OF FRAGILE-X PATIENT CELLS | 0 | 0 |
| 1425 | 15 | 24 | 1425 1995 NATURE GENETICS 10(4):483-485 LUGENBEEL KA; PEIER AM; CARSON NL; CHUDLEY AE; NELSON DL INTRAGENIC LOSS OF FUNCTION MUTATIONS DEMONSTRATE THE PRIMARY ROLE OF FMR1 IN FRAGILE-X SYNDROME | 34 | 50 |
| 1426 | 15 | 40 | 1426 1995 NATURE GENETICS 11(3):301-308 EICHLER EE; KUNST CB; LUGENBEEL KA; RYDER OA; DAVISON D; et al. EVOLUTION OF THE CRYPTIC FMR1 CGG REPEAT | 11 | 18 |
| 1427 | 27 | 61 | 1427 1995 NEUROPSYCHOLOGY 9(4):470-480 MAZZOCCO MMM; FREUND LS; BAUMGARDNER TL; FORMAN L; REISS AL NEUROPSYCHOLOGICAL AND PSYCHOSOCIAL EFFECTS OF THE FMR-1 FULL MUTATION - CASE-REPORT OF MONOZYGOTIC TWINS DISCORDANT FOR THE FRAGILE-X SYNDROME | 5 | 6 |
| 1428 | 0 | 0 | 1428 1995 NEW SCIENTIST 147(1985):10-10 WEBB J QUESTION MARK HANGS OVER FRAGILE-X TEST IN NEWBORNS | 0 | 0 |
| 1429 | 11 | 14 | 1429 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 |
| 1430 | 11 | 34 | 1430 1995 NUCLEIC ACIDS RESEARCH 23(11):1876-1881 MITCHELL JE; NEWBURY SF; MCCLELLAN JA COMPACT STRUCTURES OF D(CNG)(N) OLIGONUCLEOTIDES IN SOLUTION AND THEIR POSSIBLE RELEVANCE TO FRAGILE-X AND RELATED HUMAN GENETIC-DISEASES | 6 | 31 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1431 | 9 | 25 | 1431 1995 NUCLEIC ACIDS RESEARCH 23(20):4202-4209 USDIN K; WOODFORD KJ CGG REPEATS ASSOCIATED WITH DNA INSTABILITY AND CHROMOSOME FRAGILITY FORM STRUCTURES THAT BLOCK DNA-SYNTHESIS IN-VITRO | 22 | 100 |
| 1432 | 0 | 0 | 1432 1995 PEDIATRIC RESEARCH 38(3):431-431 DEVONDERWEID U; DAVI F; DECORTI C; CRAGNOLIN E; GLAVINA D CONTINUOUS GASTRIC INFUSION OF GLUCOSE (CGG) IN THE PREVENTION OF HYPOGLYCEMIA IN LBW INFANTS | 0 | 0 |
| 1433 | 71 | 117 | 1433 1995 PEDIATRIC RESEARCH 38(5):629-637 OOSTRA BA; HALLEY DJJ COMPLEX BEHAVIOR OF SIMPLE REPEATS - THE FRAGILE-X SYNDROME | 8 | 11 |
| 1434 | 21 | 43 | 1434 1995 PEDIATRIC RESEARCH 38(5):638-643 BERRYKRAVIS E; HICAR M; CIURLIONIS R REDUCED CYCLIC-AMP PRODUCTION IN FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR CORRELATIONS | 4 | 4 |
| 1435 | 30 | 52 | 1435 1995 PEDIATRICS 95(5):744-752 BAUMGARDNER TL; REISS AL; FREUND LS; ABRAMS MT SPECIFICATION OF THE NEUROBEHAVIORAL PHENOTYPE IN MALES WITH FRAGILE-X SYNDROME | 49 | 75 |
| 1436 | 23 | 35 | 1436 1995 PRENATAL DIAGNOSIS 15(9):801-807 CASTELLVIBEL S; MILA M; SOLER A; CARRIO A; SANCHEZ A; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - (CGG)(N) EXPANSION AND METHYLATION OF CHORIONIC VILLUS SAMPLES | 2 | 6 |
| 1437 | 2 | 18 | 1437 1995 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 92(11):5199-5203 CHEN XA; MARIAPPAN SVS; CATASTI P; RATLIFF R; MOYZIS RK; et al. HAIRPINS ARE FORMED BY THE SINGLE DNA STRANDS OF THE FRAGILE-X TRIPLET REPEATS - STRUCTURE AND BIOLOGICAL IMPLICATIONS | 33 | 161 |
| 1438 | 9 | 21 | 1438 1995 PSYCHIATRIC GENETICS 5(4):157-160 Jonsson E; Bjorck E; Wahlstrom J; Gustavsson P; Sedvall G Screening for CGG trinucleotide repeat expansion in the fragile X mental retardation 1 gene in schizophrenic patients | 0 | 1 |
| 1439 | 42 | 70 | 1439 1995 SEMINARS IN CELL BIOLOGY 6(1):5-11 NELSON DL THE FRAGILE-X SYNDROMES | 4 | 16 |
| 1440 | 15 | 19 | 1440 1996 ACTA BIOCHIMICA POLONICA 43(2):383-388 Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; et al. Analysis of unstable DNA sequence in FRM1 gene in Polish families with fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1441 | 14 | 20 | 1441 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(1):237-239 Antinolo G; Borrego S; Cabeza JC; Sanchez R; Sanchez J; et al. Reverse mutation in fragile X syndrome | 9 | 11 |
| 1442 | 6 | 13 | 1442 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(3):641-643 Brown WT; Zhong N; Dobkin C Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution | 7 | 12 |
| 1443 | 4 | 21 | 1443 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(5):906-913 Knight SJL; Ritchie RJ; Chakrabarti L; Cross G; Taylor GR; et al. A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom | 12 | 41 |
| 1444 | 18 | 37 | 1444 1996 AMERICAN JOURNAL OF HUMAN GENETICS 59(3):540-546 Vaisanen ML; Haataja R; Leisti L Decrease in the CGG(n) trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission | 5 | 9 |
| 1445 | 29 | 38 | 1445 1996 AMERICAN JOURNAL OF HUMAN GENETICS 59(6):1252-1261 Nolin SL; Lewis FA; Ye LL; Houck GE; Glicksman AE; et al. Familial transmission of the FMR1 CGG repeat | 43 | 54 |
| 1446 | 11 | 24 | 1446 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 63(2):396-400 Giampietro PF; Haas BR; Lipper E; Gutman A; Zellers NJ; et al. Fragile X syndrome in two siblings with major congenital malformations | 0 | 1 |
| 1447 | 0 | 0 | 1447 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-1 Laing S; Robinson H; Wake S; Wright F; Turner G Normal males and their role in transmission of the fragile x syndrome. | 0 | 0 |
| 1448 | 15 | 34 | 1448 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-14 Tranebjaerg L; Lubs HA; Borghgraef M; Brown WT; Fisch G; et al. Seventh International Workshop on the Fragile X and X-linked Mental Retardation | 2 | 4 |
| 1449 | 0 | 0 | 1449 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):6-6 Maes B; Borghraef M; Fryns JP Presentation of a fragile-X screening list. | 0 | 0 |
| 1450 | 0 | 0 | 1450 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):14-14 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; et al. A rare example of a reverse mutation in a fragile X syndrome family. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1451 | 0 | 0 | 1451 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):16-16 Murray A; Conway GS; Jacobs PA Premature ovarian failure and fragile X. | 0 | 0 |
| 1452 | 0 | 0 | 1452 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):17-17 Oostra BA; Willemsen R; Mandel JL; DeVries B; Devys D Rapid screening test for fragile X syndrome. | 0 | 0 |
| 1453 | 0 | 0 | 1453 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):18-18 Oostra B; DeGraaf E; Zhong N; Willemsen R Instability of the CGG repeat and expression of FMR1 protein in a male patient with a lung tumor. | 0 | 0 |
| 1454 | 0 | 0 | 1454 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):19-19 Shen Y; Zhu N; Huang D; Wu GY Studies on fragile X syndrome in the Chinese. | 0 | 0 |
| 1455 | 0 | 0 | 1455 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):25-25 deVries BBA; vandenOuweland AMW; Mohkamsing S; Halley DJJ; Tibben A; et al. Acceptance of screening for the fragile X syndrome among 1878 mentally retarded individuals in institutions and special schools in the Netherlands | 0 | 0 |
| 1456 | 4 | 21 | 1456 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):27-30 Carrel L; Willard HF An assay for X inactivation based on differential methylation at the fragile X locus, FMR1 | 1 | 32 |
| 1457 | 11 | 12 | 1457 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):176-180 Perroni L; Grasso M; Argusti A; LoNigro C; Croci GF; et al. Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families | 6 | 7 |
| 1458 | 10 | 12 | 1458 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):181-183 Spence WC; Black SH; Fallon L; Maddalena A; Cummings E; et al. Molecular fragile X screening in normal populations | 13 | 18 |
| 1459 | 9 | 10 | 1459 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):187-190 Grasso M; Perroni L; Colella S; Piombo G; Argusti A; et al. Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome | 1 | 2 |
| 1460 | 16 | 24 | 1460 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):191-195 Brown WT; Nolin S; Houck G; Ding XH; Glicksman A; et al. Prenatal diagnosis and carrier screening for fragile X by PCR | 20 | 28 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1461 | 11 | 12 | 1461 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):196-197 Turner G; Webb T; Wake S; Robinson; H Prevalence of fragile X syndrome | 153 | 235 |
| 1462 | 4 | 11 | 1462 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):198-202 Robinson H; Wake S; Wright F; Laing S; Turner G Informed choice in fragile X syndrome and its effects on prevalence | 9 | 11 |
| 1463 | 33 | 50 | 1463 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):203-208 Chiurazzi P; Macpherson J; Sherman S; Neri G Significance of linkage disequilibrium between the fragile X locus and its flanking markers | 18 | 25 |
| 1464 | 26 | 59 | 1464 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):209-215 Chiurazzi P; Genuardi M; Kozak L; GiovannucciUzielli ML; Bussani C; et al. Fragile X founder chromosomes in Italy: A few initial events and possible explanation for their heterogeneity | 17 | 26 |
| 1465 | 23 | 45 | 1465 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):220-225 Eichler EE; Nelson DL Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations | 14 | 18 |
| 1466 | 29 | 43 | 1466 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):226-233 Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; et al. Fragile X founder effects and new mutations in Finland | 14 | 26 |
| 1467 | 14 | 20 | 1467 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):234-238 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; et al. Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus | 9 | 15 |
| 1468 | 10 | 20 | 1468 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):241-245 Kooy RF; DHooge R; Reyniers E; Bakker CE; Nagels G; et al. Transgenic mouse model for the fragile X syndrome | 25 | 44 |
| 1469 | 13 | 37 | 1469 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):246-251 Godfraind JM; Reyniers E; DeBoulle K; DHooge R; DeDeyn PP; et al. Long-term potentiation in the hippocampus of fragile X knockout mice | 25 | 34 |
| 1470 | 18 | 21 | 1470 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):256-260 Sherman SL; Meadows KL; Ashley AE Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females | 13 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1471 | 19 | 28 | 1471 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):261-265 Zhong N; Ju WN; Pietrofesa J; Wang DW; Dobkin C; et al. Fragile X ''gray zone'' alleles: AGG patterns, expansion risks, and associated haplotypes | 15 | 27 |
| 1472 | 5 | 21 | 1472 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):266-267 Wohrle D; Schwemmle S; Steinbach P DNA methylation and triplet repeat stability: New proposals addressing actual questions on the CGG repeat of fragile X syndrome | 11 | 18 |
| 1473 | 13 | 17 | 1473 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):270-273 MingroniNetto RC; Haddad LA; ViannaMorgante AM The number of CGG repeats of the FMR1 locus in premutated and fully mutated heterozygotes and their offspring: Implications for the origin of mosaicism | 5 | 6 |
| 1474 | 7 | 13 | 1474 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):274-277 Steyaert J; Borghgraef M; Legius E; Fryns JP Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene | 15 | 19 |
| 1475 | 12 | 21 | 1475 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):278-282 Lachiewicz AM; Spiridigliozzi GA; McConkieRosell A; Burgess D; Feng Y; et al. A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene | 9 | 11 |
| 1476 | 23 | 35 | 1476 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):287-292 Brown WT; Houck GE; Ding XH; Zhong N; Nolin S; et al. Reverse mutations in the fragile X syndrome | 11 | 18 |
| 1477 | 16 | 20 | 1477 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):293-295 Mannermaa A; Pulkkinen L; Kajanoja E; Ryynanen M; Saarikoski S Deletion in the FMR1 gene in a fragile-X male | 9 | 9 |
| 1478 | 17 | 24 | 1478 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):296-301 Dobkin CS; Nolin SL; Cohen I; Sudhalter V; Bialer MG; et al. Tissue differences in fragile X mosaics: Mosaicism in blood cells may differ greatly from skin | 9 | 11 |
| 1479 | 29 | 43 | 1479 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):302-308 deGraaff E; deVries BBA; Willemsen R; vanHemel JO; Mohkamsing S; et al. The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells | 12 | 13 |
| 1480 | 18 | 21 | 1480 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):309-312 Maddalena A; Yadvish KN; Spence WC; HowardPeebles PN A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in blood | 13 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1481 | 4 | 9 | 1481 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):319-322 Fisch GS; Carpenter N; Maddalena A; Tarleton J; JulienInalsingh C; et al. Rater reliability of fragile X mutation size estimates: A multilaboratory analysis | 5 | 5 |
| 1482 | 12 | 31 | 1482 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):323-328 Mazzocco MMM; Holden JJA Neuropsychological profiles of three sisters homozygous for the fragile X premutation | 6 | 8 |
| 1483 | 14 | 24 | 1483 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):329-333 AllinghamHawkins DJ; Brown CA; Babul R; Chitayat D; Krekewich K; et al. Tissue-specific methylation differences and cognitive function in fragile X premutation females | 8 | 13 |
| 1484 | 12 | 18 | 1484 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):334-339 Franke P; Maier W; Hautzinger M; Weiffenbach O; Gansicke M; et al. Fragile-X carrier females: Evidence for a distinct psychopathological phenotype? | 23 | 32 |
| 1485 | 18 | 29 | 1485 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):340-345 Sobesky WE; Taylor AK; Pennington BF; Bennetto L; Porter D; et al. Molecular/clinical correlations in females with fragile X | 31 | 39 |
| 1486 | 22 | 31 | 1486 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):350-355 WrightTalamante C; Cheema A; Riddle JE; Luckey DW; Taylor AK; et al. A controlled study of longitudinal IQ changes in females and males with fragile X syndrome | 14 | 16 |
| 1487 | 15 | 41 | 1487 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):356-361 Fisch GS; Simensen R; Tarleton J; Chalifoux M; Holden JJ; et al. Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: A prospective multicenter analysis | 27 | 34 |
| 1488 | 10 | 14 | 1488 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):362-364 Fisch GS; Carpenter N; HowardPeebles PN; Maddalena A; Simensen R; et al. Lack of association between mutation size and cognitive/behavior deficits in fragile X males: A brief report | 1 | 3 |
| 1489 | 16 | 21 | 1489 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):365-369 Cohen IL; Nolin SL; Sudhalter V; Ding XH; Dobkin CS; et al. Mosaicism for the FMR1 gene influences adaptive skills development in fragile X-affected males | 15 | 16 |
| 1490 | 3 | 7 | 1490 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):370-372 Partington MW; Moore DY; Turner GM Confirmation of early menopause in fragile X carriers | 26 | 44 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1491 | 2 | 2 | 1491 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):376-376 Burgess B; Partington M; Turner G; Robinson H Normal age of menarche in fragile X syndrome | 3 | 3 |
| 1492 | 4 | 6 | 1492 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):377-377 HowardPeebles PN Successful pregnancy in a fragile X carrier by donor egg | 2 | 3 |
| 1493 | 0 | 7 | 1493 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):378-381 Wingrove EJ; Norris J; Barton PL; Hagerman R Experiences and attitudes concerning genetic testing and insurance in a Colorado population: A survey of families diagnosed with fragile X syndrome | 0 | 9 |
| 1494 | 3 | 18 | 1494 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):395-398 Piussan C; Mathieu M; Berquin P; Fryns JP Fragile X mutation and FG syndrome-like phenotype | 1 | 4 |
| 1495 | 14 | 19 | 1495 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):404-407 Kambouris M; Snow K; Thibodeau S; Bluhm D; Green M; et al. Segregation of the fragile X mutation from a male with a full mutation: Unusual somatic instability in the FMR-1 locus | 1 | 3 |
| 1496 | 12 | 20 | 1496 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):413-414 Loesch DZ Fragile X: Clinical associations | 0 | 0 |
| 1497 | 16 | 25 | 1497 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):428-433 Meadows KL; Pettay D; Newman J; Hersey J; Ashley AE; et al. Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population | 13 | 27 |
| 1498 | 1 | 1 | 1498 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(3):527-527 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; et al. Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus (vol 64, pg 234, 1996) | 0 | 0 |
| 1499 | 0 | 3 | 1499 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 65(4):355-356 Seemanova E Fragile X syndrome in incestuous families | 0 | 0 |
| 1500 | 1 | 1 | 1500 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 66(1):118-118 Perroni L; Grasso M; Argusti A; Nigro CL; Croci GF; et al. Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families (vol 64, pg 176, 1996) | 0 | 0 |