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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.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1301 | 28 | 92 | 1301 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(6):480-493 Schapiro MB; Murphy DGM; Hagerman RJ; Azari NP; Alexander GE; Miezejeski CM; Hinton VJ; Horwitz B; Haxby JV; Kumar A; White B; Grady CL Adult fragile X syndrome: Neuropsychology, brain anatomy, and metabolism | 19 | 29 |
| 1302 | 12 | 24 | 1302 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 |
| 1303 | 0 | 0 | 1303 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 |
| 1304 | 70 | 125 | 1304 1995 ANNUAL REVIEW OF NEUROSCIENCE 18:77-99 WARREN ST; ASHLEY CT TRIPLET REPEAT EXPANSION MUTATIONS - THE EXAMPLE OF FRAGILE-X SYNDROME | 24 | 56 |
| 1305 | 27 | 43 | 1305 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):3-5 TURK J FRAGILE-X SYNDROME | 2 | 4 |
| 1306 | 16 | 30 | 1306 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):33-37 SLANEY SF; WILKIE AOM; HIRST MC; CHARLTON R; MCKINLEY M; POINTON J; CHRISTODOULOU Z; HUSON SM; DAVIES KE DNA TESTING FOR FRAGILE-X SYNDROME IN SCHOOLS FOR LEARNING-DIFFICULTIES | 12 | 20 |
| 1307 | 2 | 5 | 1307 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(6):544-544 TURK J TREATMENT OF FRAGILE-X SYNDROME | 0 | 0 |
| 1308 | 11 | 19 | 1308 1995 ARCHIVES OF MEDICAL RESEARCH 26:S77-S83 DiazGallardo MY; BarrosNunez P; Diaz CA; Hernandez A; GomezEspinel I; Leal CA; Fragoso R; Figuera L; GarciaCruz D; RamirezDuenas ML; Cantu JM Molecular characterization of the fragile-X syndrome in the Mexican population | 2 | 4 |
| 1309 | 39 | 112 | 1309 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 |
| 1310 | 0 | 0 | 1310 1995 BIOLOGICAL PSYCHIATRY 37(9):629-629 REISS AL FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1311 | 2 | 6 | 1311 1995 BONE MARROW TRANSPLANTATION 16(4):625-626 MORTON J; ARNOLD L; FLETCHER B; MCCARTHY C; ROWELL J; DURRANT S ALLOGENEIC BMT FROM A DONOR WITH FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR EVALUATION | 0 | 0 |
| 1312 | 26 | 39 | 1312 1995 BRAIN & DEVELOPMENT 17(5):317-321 NANBA E; KOHNO Y; MATSUDA A; YANO M; SATO C; HASHIMOTO K; KOEDA T; YOSHINO K; KIMURA M; MAEOKA Y; YAMAMOTO T; MAEGAKI Y; EDA I; TAKESHITA K NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED JAPANESE MALES | 5 | 15 |
| 1313 | 4 | 5 | 1313 1995 BRAIN & DEVELOPMENT 17(5):322-322 NAKAHORI Y THE INCIDENCE OF THE FRAGILE-X SYNDROME IN JAPANESE - COMMENTARY ON NANBAS PAPER | 0 | 0 |
| 1314 | 4 | 7 | 1314 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 |
| 1315 | 0 | 0 | 1315 1995 BRAIN AND COGNITION 28(1):111-111 GRIGSBY J; KAYE K VARIABLE EXPRESSION OF DEVELOPMENTAL GERSTMANN SIGNS IN FRAGILE-X SYNDROME | 0 | 0 |
| 1316 | 0 | 0 | 1316 1995 BRAIN AND COGNITION 28(1):111-112 GRIGSBY J; KAYE K DISSOCIATIONS IN DEVELOPMENTAL DYSCALCULIA SECONDARY TO FRAGILE-X SYNDROME | 0 | 0 |
| 1317 | 0 | 1 | 1317 1995 BRITISH JOURNAL OF PSYCHIATRY 166:688-688 COOKE LB BEHAVIOR AND DEVELOPMENT IN FRAGILE-X SYNDROME - DYKENS,E | 0 | 0 |
| 1318 | 0 | 1 | 1318 1995 BRITISH MEDICAL JOURNAL 310(6973):148-148 CRAFT N STUDY SUPPORTS SCREENING FOR THE FRAGILE-X-SYNDROME | 2 | 3 |
| 1319 | 0 | 0 | 1319 1995 CLINICAL CHEMISTRY 41(11):30-30 RADU DN; CHIANG CS RAPID, NONRADIOACTIVE SOUTHERN BLOT METHOD FOR DETECTING FRAGILE-X MUTATIONS | 0 | 0 |
| 1320 | 43 | 78 | 1320 1995 CLINICS IN LABORATORY MEDICINE 15(4):859-& Brown WT Perspectives and molecular diagnosis of the fragile X syndrome | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1321 | 0 | 0 | 1321 1995 CYTOGENETICS AND CELL GENETICS 69(1-2):116-116 HOWARDPEEBLES PN IT IS TIME TO ABANDON THE CYTOGENETIC FRAGILE-X TEST | 0 | 0 |
| 1322 | 9 | 23 | 1322 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):167-184 Hagerman R; Staley L; Brown WT; Taylor A; Meadow K; Dorn M; Stoorman S; Neri G; Chiurazzi P; Levitas A; Spiridigliozzi GA; OConnor R; Weber JD; Braden M; Sudhalter V Conference summary: Fourth International Conference on Fragile X and X-linked Mental Retardation sponsored by the National Fragile X Foundation | 0 | 0 |
| 1323 | 0 | 0 | 1323 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):185-186 Nommensen D Report of the Executive Director of the National Fragile X Foundation | 0 | 0 |
| 1324 | 32 | 75 | 1324 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):187-198 Abrams MT; Reiss AL Quantitative brain imaging studies of fragile X syndrome | 2 | 3 |
| 1325 | 46 | 131 | 1325 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):199-217 Binstock TC Fragile X and the amygdala: Cognitive, interpersonal, emotional, and neuroendocrine considerations | 4 | 4 |
| 1326 | 3 | 16 | 1326 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):218-222 Musumeci SA; Ferri R; Elia M; DalGracco S; Scuderi C; Stefanini MC; Castano A; Azan G Sleep neurophysiology in fragile X patients | 2 | 3 |
| 1327 | 10 | 22 | 1327 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):223-229 King RA; Hagerman R; Houghton M Ocular findings in fragile X syndrome | 1 | 1 |
| 1328 | 27 | 36 | 1328 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):230-241 Brun C; Obiols JE; Cheema A; OConnor R; Riddle J; DiMaria M; WrightTalamante C; Hagerman R Longitudinal IQ changes in fragile X females | 1 | 1 |
| 1329 | 17 | 33 | 1329 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 | 15 | 20 |
| 1330 | 40 | 75 | 1330 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):252-269 Cohen IL Behavioral profiles of autistic and nonautistic fragile X males | 11 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1331 | 15 | 38 | 1331 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):270-279 Belser RC; Sudhalter V Arousal difficulties in males with fragile X syndrome: A preliminary report | 20 | 24 |
| 1332 | 19 | 37 | 1332 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):280-292 Sobesky WE; Porter D; Pennington BF; Hagerman RJ Dimensions of shyness in fragile X females | 12 | 17 |
| 1333 | 24 | 41 | 1333 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):293-301 Jenkins EC; Houck GE; Ding XH; Li SY; StarkHouck SL; Salerno J; Genovese M; Glicksman A; Nolin SL; Zhong N; Brooks SLS; Dobkin CS; Brown WT An update on fragile X prenatal diagnosis: End of the cytogenetic testing era | 1 | 1 |
| 1334 | 11 | 21 | 1334 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 |
| 1335 | 10 | 25 | 1335 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 |
| 1336 | 8 | 35 | 1336 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 | 10 | 10 |
| 1337 | 2 | 23 | 1337 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 |
| 1338 | 0 | 7 | 1338 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):359-362 Lin JFH Introduction to fragile X syndrome for parents | 0 | 0 |
| 1339 | 0 | 0 | 1339 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):363-366 Glass L Females with fragile X: A parent's perspective | 0 | 0 |
| 1340 | 5 | 9 | 1340 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1341 | 0 | 0 | 1341 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):390-395 McConkieRosell A; Robinson H; Wake S; Staley L; Heller K; Cronister A Educating extended family members about the inheritance of the fragile X syndrome | 0 | 1 |
| 1342 | 7 | 18 | 1342 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):396-404 Mazzocco MMM; Lachiewicz AM; Kovar CG; Freund LS; Baumgardner TL; Dykens E Psychological and emotional studies of the fragile X mutation - A workshop summary | 0 | 0 |
| 1343 | 5 | 9 | 1343 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):408-410 HowardPeebles PN; Maddalena A; Black SH; Levinson G; Bick DP; Schulman JD Fragile X screening in pediatric and obstetrical patients | 2 | 2 |
| 1344 | 0 | 0 | 1344 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 |
| 1345 | 13 | 16 | 1345 1995 DIAGNOSTIC MOLECULAR PATHOLOGY 4(3):158-161 NABER SP MOLECULAR DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| 1346 | 13 | 43 | 1346 1995 EMBO JOURNAL 14(11):2401-2408 SIOMI MC; SIOMI H; SAUER WH; SRINIVASAN S; NUSSBAUM RL; DREYFUSS G FXR1, AN AUTOSOMAL HOMOLOG OF THE FRAGILE-X MENTAL-RETARDATION GENE | 51 | 95 |
| 1347 | 16 | 36 | 1347 1995 EMBO JOURNAL 14(21):5358-5366 ZHANG Y; OCONNOR JP; SIOMI MC; SRINIVASAN S; DUTRA A; NUSSBAUM RL; DREYFUSS G THE FRAGILE-X MENTAL-RETARDATION SYNDROME PROTEIN INTERACTS WITH NOVEL HOMOLOGS FXR1 AND FXR2 | 63 | 111 |
| 1348 | 0 | 0 | 1348 1995 EPILEPSIA 36:S1-S1 KLUGER G; BOHM I; LAUB MC; WALDENMEIER C; STUHRMANNSPANGENBERG M EEG IN CHILDREN WITH FRAGILE-X PREMUTATION | 0 | 0 |
| 1349 | 0 | 0 | 1349 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 |
| 1350 | 0 | 0 | 1350 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1351 | 3 | 4 | 1351 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 |
| 1352 | 2 | 9 | 1352 1995 GENETIC COUNSELING 6(3):207-210 ALEMBIK Y; DOTT B; STOLL C RETT-LIKE SYNDROME IN FRAGILE-X SYNDROME | 1 | 6 |
| 1353 | 1 | 4 | 1353 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 |
| 1354 | 12 | 26 | 1354 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 |
| 1355 | 17 | 33 | 1355 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 |
| 1356 | 20 | 28 | 1356 1995 HUMAN GENETICS 96(5):577-584 ELALEEM AA; BOHM I; TEMTAMY S; ELAWADY M; AWADALLA M; SCHMIDTKE J; STUHRMANN M 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 | 5 | 9 |
| 1357 | 25 | 49 | 1357 1995 HUMAN MOLECULAR GENETICS 4(1):45-49 DEGRAAFF E; ROUILLARD P; WILLEMS PJ; SMITS APT; ROUSSEAU F; OOSTRA BA HOTSPOT FOR DELETIONS IN THE CGG REPEAT REGION OF FMR1 IN FRAGILE-X PATIENTS | 27 | 46 |
| 1358 | 18 | 31 | 1358 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 | 7 | 13 |
| 1359 | 8 | 11 | 1359 1995 ISRAEL JOURNAL OF MEDICAL SCIENCES 31(5):323-325 DAR H; SCHAAP T; BAITOR H; BOROCHOWITZ Z; GELMANKOHAN Z; CHEMKE T; CHAKI R; COHEN H; FALIKBORENSTEIN Z; CHEMKE J ETHNIC DISTRIBUTION OF THE FRAGILE-X SYNDROME IN ISRAEL - EVIDENCE OF FOUNDER CHROMOSOMES() | 1 | 1 |
| 1360 | 5 | 24 | 1360 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 |
| 1361 | 15 | 46 | 1361 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 | 11 | 47 |
| 1362 | 0 | 0 | 1362 1995 JOURNAL OF CELLULAR BIOCHEMISTRY :373-373 WILLEMS PJ; BAKKER CE; REYNIERS E; VERHEIJ C; DEBOULLE K; OOSTRA BA A TRANSGENIC MOUSE MODEL FOR FRAGILE-X SYNDROME | 0 | 0 |
| 1363 | 0 | 1 | 1363 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 |
| 1364 | 22 | 37 | 1364 1995 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 17(4):518-528 HINTON VJ; HALPERIN JM; DOBKIN CS; DING XH; BROWN WT; MIEZEJESKI CM COGNITIVE AND MOLECULAR ASPECTS OF FRAGILE-X | 5 | 7 |
| 1365 | 2 | 14 | 1365 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:326-330 SIMON EW; RAPPAPORT DA; PAPKA M; WOODRUFFPAK DS FRAGILE-X AND DOWNS-SYNDROME - ARE THERE SYNDROME-SPECIFIC COGNITIVE PROFILES AT LOW IQ LEVELS | 2 | 4 |
| 1366 | 15 | 26 | 1366 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 |
| 1367 | 0 | 0 | 1367 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 | 1 | 2 |
| 1368 | 0 | 0 | 1368 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 |
| 1369 | 0 | 0 | 1369 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 |
| 1370 | 0 | 0 | 1370 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1371 | 10 | 20 | 1371 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 | 15 | 27 |
| 1372 | 16 | 27 | 1372 1995 JOURNAL OF MEDICAL GENETICS 32(3):236-239 MACPHERSON JN; CURTIS G; CROLLA JA; DENNIS N; MIGEON B; GREWAL PK; HIRST MC; DAVIES KE; JACOBS PA UNUSUAL (CGG)(N) EXPANSION AND RECOMBINATION IN A FAMILY WITH FRAGILE-X AND DIGEORGE-SYNDROME | 3 | 11 |
| 1373 | 16 | 40 | 1373 1995 JOURNAL OF MEDICAL GENETICS 32(10):764-769 DEVRIES BBA; ROBINSON H; STOLTEDIJKSTRA I; GI CVTP; DIJKSTRA PF; VANDOOM J; HALLEY DJJ; OOSTRA BA; TURNER G; NIERMEIJER MF GENERAL OVERGROWTH IN THE FRAGILE-X SYNDROME - VARIABILITY IN THE PHENOTYPIC-EXPRESSION OF THE FMR1 GENE MUTATION | 6 | 15 |
| 1374 | 8 | 12 | 1374 1995 JOURNAL OF MEDICAL GENETICS 32(11):907-908 PINTADO E; DEDIEGO Y; HMADCHA A; CARRASCO M; SIERRA J; LUCAS M INSTABILITY OF THE CGG REPEAT AT THE FRAXA LOCUS AND VARIABLE PHENOTYPIC-EXPRESSION IN A LARGE FRAGILE-X PEDIGREE | 2 | 9 |
| 1375 | 13 | 35 | 1375 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 | 12 |
| 1376 | 11 | 67 | 1376 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 | 12 | 95 |
| 1377 | 8 | 9 | 1377 1995 LANCET 345(8958):1147-1148 WILLEMSEN R; MOHKAMSING S; DEVRIES B; DEVYS D; VANDENOUWELAND A; MANDEL JL; GALJAARD H; OOSTRA B RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME | 73 | 94 |
| 1378 | 2 | 5 | 1378 1995 LANCET 346(8970):309-310 CONWAY GS; HETTIARACHCHI S; MURRAY A; JACOBS PA FRAGILE-X PREMUTATIONS IN FAMILIAL PREMATURE OVARIAN FAILURE | 19 | 41 |
| 1379 | 35 | 59 | 1379 1995 MEDICINA-BUENOS AIRES 55(5):457-466 BANARES VG UPDATING THE FRAGILE-X SYNDROME | 0 | 0 |
| 1380 | 0 | 0 | 1380 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1381 | 15 | 24 | 1381 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 | 30 | 49 |
| 1382 | 27 | 61 | 1382 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 |
| 1383 | 0 | 0 | 1383 1995 NEW SCIENTIST 147(1985):10-10 WEBB J QUESTION MARK HANGS OVER FRAGILE-X TEST IN NEWBORNS | 0 | 0 |
| 1384 | 11 | 14 | 1384 1995 NEW ZEALAND MEDICAL JOURNAL 108(1009):404-406 NEVILLE L; COCHRANE J; FITZGERALD P; KENNEDY M FRAGILE-X MENTAL-RETARDATION SYNDROME - DNA DIAGNOSIS AND CARRIER DETECTION IN NEW-ZEALAND FAMILIES | 0 | 0 |
| 1385 | 11 | 34 | 1385 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 | 2 | 31 |
| 1386 | 68 | 117 | 1386 1995 PEDIATRIC RESEARCH 38(5):629-637 OOSTRA BA; HALLEY DJJ COMPLEX BEHAVIOR OF SIMPLE REPEATS - THE FRAGILE-X SYNDROME | 7 | 11 |
| 1387 | 19 | 43 | 1387 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 | 3 | 4 |
| 1388 | 30 | 52 | 1388 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 | 46 | 71 |
| 1389 | 23 | 35 | 1389 1995 PRENATAL DIAGNOSIS 15(9):801-807 CASTELLVIBEL S; MILA M; SOLER A; CARRIO A; SANCHEZ A; VILLA M; JIMENEZ MD; ESTIVILL X PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - (CGG)(N) EXPANSION AND METHYLATION OF CHORIONIC VILLUS SAMPLES | 2 | 6 |
| 1390 | 2 | 18 | 1390 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; LAAYOUN A; SMITH SS; BRADBURY EM; GUPTA G HAIRPINS ARE FORMED BY THE SINGLE DNA STRANDS OF THE FRAGILE-X TRIPLET REPEATS - STRUCTURE AND BIOLOGICAL IMPLICATIONS | 25 | 154 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1391 | 9 | 21 | 1391 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 |
| 1392 | 40 | 70 | 1392 1995 SEMINARS IN CELL BIOLOGY 6(1):5-11 NELSON DL THE FRAGILE-X SYNDROMES | 3 | 16 |
| 1393 | 15 | 19 | 1393 1996 ACTA BIOCHIMICA POLONICA 43(2):383-388 Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; Bocian E; Halley DJJ; Horst J; Mazurczak T Analysis of unstable DNA sequence in FRM1 gene in Polish families with fragile X syndrome | 0 | 0 |
| 1394 | 14 | 20 | 1394 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(1):237-239 Antinolo G; Borrego S; Cabeza JC; Sanchez R; Sanchez J; Sanchez B Reverse mutation in fragile X syndrome | 7 | 11 |
| 1395 | 6 | 13 | 1395 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 | 6 | 12 |
| 1396 | 4 | 21 | 1396 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(5):906-913 Knight SJL; Ritchie RJ; Chakrabarti L; Cross G; Taylor GR; Mueller RF; Hurst J; Paterson J; Yates JRW; Dow DJ; Davies KE A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom | 11 | 41 |
| 1397 | 15 | 37 | 1397 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 | 4 | 9 |
| 1398 | 11 | 24 | 1398 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 63(2):396-400 Giampietro PF; Haas BR; Lipper E; Gutman A; Zellers NJ; LaTrenta GS; Brooks SS; Matalon R; Kaul R; Ding XH; Brown WT Fragile X syndrome in two siblings with major congenital malformations | 0 | 1 |
| 1399 | 0 | 0 | 1399 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 |
| 1400 | 15 | 34 | 1400 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-14 Tranebjaerg L; Lubs HA; Borghgraef M; Brown WT; Fisch G; Fryns JP; Hagerman R; Jacobs PA; Mandel JL; Mulley J; Oostra B; Schwartz C; Sherman S; Willard H; Willems P Seventh International Workshop on the Fragile X and X-linked Mental Retardation | 2 | 4 |
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