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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by NCR.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1301 | 4 | 11 | 266 1985 CLINICAL GENETICS 28(2):97-99 ABUELO D; CASTREE K; PUESCHEL S; PADREMENDOZA T; ZOLNIERZ K FREQUENCY OF FRAGILE X-CHROMOSOME IN NORMAL FEMALES | 2 | 5 |
| 1302 | 4 | 11 | 309 1985 SEMAINE DES HOPITAUX 61(25):1807-1809 LEJEUNE J; RETHORE MO; DEBLOIS MC; RAVEL A ASSAY OF FOLIC-ACID TREATMENT IN FRAGILE-X SYNDROME | 0 | 0 |
| 1303 | 5 | 11 | 320 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):171-178 SIMPSON NE DERMATOGLYPHIC INDEXES OF MALES WITH THE FRAGILE-X SYNDROME AND OF THE FEMALE HETEROZYGOTES | 6 | 10 |
| 1304 | 4 | 11 | 324 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):207-211 WILLIAMS CA; CANTU ES; FRIAS JL BRIEF CLINICAL REPORT - METAPHYSEAL DYSOSTOSIS AND CONGENITAL NYSTAGMUS IN A MALE INFANT WITH THE FRAGILE-X SYNDROME | 2 | 6 |
| 1305 | 5 | 11 | 342 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):511-514 HOWARDPEEBLES PN METHIONINE METABOLISM AND FRAGILE-X EXPRESSION | 0 | 4 |
| 1306 | 4 | 11 | 349 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):589-595 SANFILIPPO S; RAGUSA RM; MUSUMECI S; NERI G FRAGILE-X MENTAL-RETARDATION - PREVALENCE IN A GROUP OF INSTITUTIONALIZED PATIENTS IN ITALY AND DESCRIPTION OF A NOVEL EEG PATTERN | 15 | 22 |
| 1307 | 3 | 11 | 368 1986 BRITISH JOURNAL OF PSYCHIATRY 148:655-657 PRIMROSE DA; ELMATMATI R; BOYD E; GOSDEN C; NEWTON M PREVALENCE OF THE FRAGILE-X SYNDROME IN AN INSTITUTION FOR THE MENTALLY-HANDICAPPED | 16 | 22 |
| 1308 | 4 | 11 | 393 1986 JOURNAL OF MEDICAL GENETICS 23(5):396-399 WEBB TP; BUNDEY S; THAKE A; TODD J THE FREQUENCY OF THE FRAGILE X-CHROMOSOME AMONG SCHOOLCHILDREN IN COVENTRY | 68 | 105 |
| 1309 | 4 | 11 | 459 1987 HUMAN GENETICS 77(1):92-94 ARINAMI T; KONDO I; HAMAGUCHI H; TAMURA K; HIRANO T A FRAGILE-X FEMALE WITH DOWN-SYNDROME | 8 | 11 |
| 1310 | 6 | 11 | 518 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):177-183 MILONE G; CONTI L; RIZZO R; SANFILIPPO S; SAMMITO V; ROMANO C A DERMATOGLYPHIC STUDY OF A GROUP OF SICILIAN CHILDREN WITH FRAGILE-X SYNDROME | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1311 | 1 | 11 | 599 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(4):681-685 TSAI LY; CROWE RR; PATIL SR; MURRAY J; QUINN J SEARCH FOR DNA MARKERS IN 2 AUTISTIC MALES WITH THE FRAGILE-X SYNDROME | 2 | 3 |
| 1312 | 5 | 11 | 717 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(1):1-2 GOODYEAR HM; SONKSON PM FRAGILE X-SYNDROME - AN IMPORTANT CAUSE OF MENTAL-RETARDATION | 0 | 0 |
| 1313 | 7 | 11 | 725 1990 PATHOBIOLOGY 58(4):236-240 JENKINS EC; DUNCAN CJ; SANZ MM; GENOVESE M; GU H; SCHWARTZRICHSTEIN C; LELE KP; SALANDI ML; KRAWCZUN MS PROGRESS TOWARD AN INTERNAL CONTROL-SYSTEM FOR FRAGILE-X INDUCTION BY 5-FLUORODEOXYURIDINE IN WHOLE-BLOOD CULTURES | 3 | 6 |
| 1314 | 7 | 11 | 798 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):363-366 DRUGGE U; BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY OF POSSIBLY AFFECTED INDIVIDUALS IN THE 19TH-CENTURY | 2 | 2 |
| 1315 | 4 | 11 | 815 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):453-455 SHAPIRO LR; WILMOT PL; MURPHY PD PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - POSSIBLE END OF THE EXPERIMENTAL PHASE FOR AMNIOTIC-FLUID | 5 | 6 |
| 1316 | 7 | 11 | 884 1991 NATURE 351(6326):439-440 DAVIES K HUMAN-GENETICS - BREAKING THE FRAGILE-X | 2 | 7 |
| 1317 | 6 | 11 | 886 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1720-1722 SUTHERLAND GR; GEDEON A; KORNMAN L; DONNELLY A; BYARD RW; MULLEY JC; KREMER E; LYNCH M; PRITCHARD M; YU S; RICHARDS RI PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT DETECTION OF THE UNSTABLE DNA-SEQUENCE | 61 | 86 |
| 1318 | 7 | 11 | 887 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1736-1738 SHAPIRO LR THE FRAGILE X-SYNDROME - A PECULIAR PATTERN OF INHERITANCE | 2 | 5 |
| 1319 | 5 | 11 | 916 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):96-102 BROWN WT; JENKINS EC; GOONEWARDENA P; MIEZEJESKI C; ATKIN J; DEVYS D PRENATALLY DETECTED FRAGILE-X FEMALES - LONG-TERM FOLLOW-UP-STUDIES SHOW HIGH-RISK OF MENTAL IMPAIRMENT | 4 | 4 |
| 1320 | 7 | 11 | 950 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(5):905-912 MACPHERSON J; HARVEY J; CURTIS G; WEBB T; HEITZ D; ROUSSEAU F; JACOBS P A REINVESTIGATION OF 33 FRAGILE(X) FAMILIES USING PROBE STB12.3 | 7 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1321 | 5 | 11 | 966 1992 BRITISH MEDICAL JOURNAL 305(6847):208-208 MOORE DWY NEW DEVELOPMENTS IN THE FRAGILE-X SYNDROME | 1 | 1 |
| 1322 | 1 | 11 | 1062 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(6):685-686 MIGEON BR ROLE OF DNA METHYLATION IN X-INACTIVATION AND THE FRAGILE X-SYNDROME | 2 | 3 |
| 1323 | 7 | 11 | 1080 1993 CLINICAL GENETICS 44(2):109-110 BODURTHA J; JACKSONCOOK C; MADDALENA A; PISERCHIO J; WALLER R 46XY/47XYY MOSAICISM AND FRAGILE-X | 3 | 4 |
| 1324 | 10 | 11 | 1115 1993 JOURNAL OF MEDICAL GENETICS 30(3):193-197 KNOBLOCH O; PELZ F; WICK U; NELSON DL; ZOLL B DIRECT VERSUS INDIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X MENTAL-RETARDATION IN 40 GERMAN FAMILIES AT RISK | 1 | 1 |
| 1325 | 4 | 11 | 1191 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 | 19 | 41 |
| 1326 | 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 |
| 1327 | 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 |
| 1328 | 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 |
| 1329 | 4 | 11 | 1413 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 |
| 1330 | 3 | 11 | 1555 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 69(1):114-116 Martin NG; Healey SC; Pangan TS; Heath AC; Turner G Do mothers of dizygotic twins have earlier menopause? A role for fragile X? | 5 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1331 | 4 | 11 | 1573 1997 BRITISH MEDICAL JOURNAL 315(7117):1174-1175 Barnicoat A Screening for fragile X syndrome: a model for genetic disorders? | 1 | 4 |
| 1332 | 6 | 11 | 1696 1998 NEUROREPORT 9(3):477-481 Steward O; Bakker CE; Willems PJ; Oostra BA No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome | 10 | 16 |
| 1333 | 5 | 11 | 1738 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):327-328 Braat DDM; Smits APT; Thomas CMG Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: A pilot study | 8 | 11 |
| 1334 | 6 | 11 | 1740 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):338-341 Dobkin C; Ding XH; Li SY; Houck G; Nolin SL; Glicksman A; Zhong N; Jenkins EC; Brown WT Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection | 2 | 3 |
| 1335 | 4 | 11 | 1758 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):306-308 Syrrou M; Georgiou I; Patsalis PC; Bouba I; Adonakis G; Papoulatos GN Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction | 1 | 9 |
| 1336 | 3 | 11 | 1860 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):358-360 Missirian C; Moncla A; Voelckel MA; Ravix V; Philip N Fragile X syndrome and 22q11.2 microdeletion in the same sibship | 0 | 0 |
| 1337 | 1 | 10 | 133 1983 CYTOGENETICS AND CELL GENETICS 35(3):223-225 BRYANT EM; MARTIN GM; HOEHN H FRAGILE-X EXPRESSION STUDIED BY CLONAL ANALYSIS AND SOMATIC-CELL HYBRIDIZATION | 9 | 12 |
| 1338 | 3 | 10 | 140 1983 JOURNAL DE GENETIQUE HUMAINE 31(2):133-139 JALBERT H; BAETEMAN MA; TROCHETROYER C; MATTEI MG; MATTEI JF; LEROUX D; JALBERT P MENTAL-RETARDATION WITH FRAGILE-X - NEITHER INACTIVATION NOR DELETION OF THE SEGMENT Q28-]Q TER ENZYMATIC AND MORPHOMETRIC DATA | 0 | 0 |
| 1339 | 2 | 10 | 204 1984 HUMAN GENETICS 68(2):189-190 REIDY JA; CHEN ATL FOLIC-ACID AND CHROMOSOME BREAKAGE .2. A METHIONINE EFFECT SIMILAR TO THAT IN FRAGILE-X EXPRESSION | 1 | 9 |
| 1340 | 4 | 10 | 252 1985 AMERICAN JOURNAL OF PSYCHIATRY 142(1):108-110 GOLDFINE PE; MCPHERSON PM; HEATH GA; HARDESTY VA; BEAUREGARD LJ; GORDON B ASSOCIATION OF FRAGILE-X SYNDROME WITH AUTISM | 35 | 52 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1341 | 2 | 10 | 305 1985 LANCET 1(8433):871-871 OBERLE I; MANDEL JL; BOUE J; MATTEI MG; MATTEI JF POLYMORPHIC DNA MARKERS IN PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 14 | 27 |
| 1342 | 1 | 10 | 348 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):581-587 GUSTAVSON KH; BLOMQUIST H; HOLMGREN G PREVALENCE OF THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED BOYS IN A SWEDISH COUNTY | 52 | 74 |
| 1343 | 0 | 10 | 358 1986 ANNALES DE GENETIQUE 29(4):261-263 BELGHITI D; RAZAVIENCHA F; RAOUL O; HIRBEC G; GUILLOT F; REINERT P; SOBEL A COINCIDENCE OF FAMILIAL SYSTEMIC LUPUS-ERYTHEMATOSUS AND THE FRAGILE-X SYNDROME | 0 | 3 |
| 1344 | 6 | 10 | 418 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(3):731-732 CARPENTER NJ; VEENEMA H; BAKKER E; HOFKER MH; PEARSON PL A NEW DNA PROBE PROXIMAL TO AND CLOSELY LINKED TO FRAGILE-X | 4 | 4 |
| 1345 | 6 | 10 | 482 1987 LANCET 1(8527):280-280 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; JENKINS EC RFLP FOR LINKAGE ANALYSIS OF FRAGILE-X SYNDROME | 21 | 35 |
| 1346 | 6 | 10 | 547 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):665-672 NERI G; SANFILIPPO S; PAVONE L; MOLLICA F; BARBERI I; GIUFFRE L; ROMANO C; MATTINA T; CAMMARATA M; RAGUSA MG; SAMMITO V; VENTIMIGLIA G; MUSUMECI SA THE FRAGILE-X IN SICILY - AN EPIDEMIOLOGICAL SURVEY | 9 | 16 |
| 1347 | 2 | 10 | 558 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):779-781 BUTLER MG; NAJJAR JL DO SOME PATIENTS WITH FRAGILE-X SYNDROME HAVE PRECOCIOUS PUBERTY | 13 | 15 |
| 1348 | 4 | 10 | 614 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):977-978 FERRI R BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME | 2 | 3 |
| 1349 | 2 | 10 | 632 1989 CYTOGENETICS AND CELL GENETICS 50(2-3):172-173 SAUER SM; PHELAN MC; RICHER CL; SCHWARTZ CE PHYSICAL MAPPING OF PROBES PROXIMAL TO THE FRAGILE-X LOCUS (FRAX) CONFIRMS THE ORDER F9-DXS105 (CX55.7)-DXS98 (4D8)-FRAXA | 1 | 1 |
| 1350 | 3 | 10 | 721 1990 NEUROLOGY 40(2):378-380 DESAI HB; DONAT J; SHOKEIR MHK; MUNOZ DG AMYOTROPHIC LATERAL SCLEROSIS IN A PATIENT WITH FRAGILE X-SYNDROME | 5 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1351 | 3 | 10 | 825 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):511-513 MUSUMECI SA; FERRI R; ELIA M; COLOGNOLA RM; BERGONZI P; TASSINARI CA EPILEPSY AND FRAGILE-X SYNDROME - A FOLLOW-UP-STUDY | 21 | 36 |
| 1352 | 5 | 10 | 842 1991 CLINICAL GENETICS 39(5):347-354 BUTLER MG; MANGRUM T; GUPTA R; SINGH DN A 15-ITEM CHECKLIST FOR SCREENING MENTALLY-RETARDED MALES FOR THE FRAGILE X-SYNDROME | 28 | 32 |
| 1353 | 5 | 10 | 863 1991 HUMAN GENETICS 87(4):503-505 STEEN AM; MARCUS S; SAHLEN S; NIELSEN KB; LAMBERT B THE FRAGILE-X MUTATION DOES NOT HAVE ANY MAJOR EFFECT ON THE EXPRESSION OF THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE (HPRT) LOCUS IN HUMAN FIBROBLASTS | 0 | 2 |
| 1354 | 5 | 10 | 871 1991 JOURNAL OF MEDICAL GENETICS 28(12):818-823 RICHARDS RI; HOLMAN K; KOZMAN H; KREMER E; LYNCH M; PRITCHARD M; YU S; MULLEY J; SUTHERLAND GR FRAGILE-X SYNDROME - GENETIC LOCALIZATION BY LINKAGE MAPPING OF 2 MICROSATELLITE REPEATS FRAXAC1 AND FRAXAC2 WHICH IMMEDIATELY FLANK THE FRAGILE SITE | 52 | 100 |
| 1355 | 6 | 10 | 919 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):120-123 PARTINGTON MW; ROBINSON H; LAING S; TURNER G MORTALITY IN THE FRAGILE-X SYNDROME - PRELIMINARY DATA | 2 | 3 |
| 1356 | 6 | 10 | 986 1992 JAPANESE JOURNAL OF HUMAN GENETICS 37(3):195-203 YAMAUCHI M; SEKI N; HORI TA RAPID PREPARATION OF DIAGNOSTIC PROBES FOR THE FRAGILE-X SYNDROME BY DIRECT PCR AMPLIFICATION OF HUMAN CHROMOSOMAL DNA | 4 | 7 |
| 1357 | 3 | 10 | 992 1992 JOURNAL OF MEDICAL GENETICS 29(8):599-599 TIZZANO EF; BAIGET M HIGH PROPORTION OF TWINS IN CARRIERS OF FRAGILE X-SYNDROME | 3 | 4 |
| 1358 | 8 | 10 | 998 1992 LANCET 339(8788):271-272 PERGOLIZZI RG; ERSTER SH; GOONEWARDENA P; BROWN WT DETECTION OF FULL FRAGILE-X MUTATION | 46 | 69 |
| 1359 | 2 | 10 | 1146 1993 SCIENTIST 7(19):16-16 CASKEY CT HOT PAPERS - MOLECULAR-GENETICS - VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX BY FU,Y.H., KUHL,D.P.A., PIZZUTI,A., ET-AL, AND AN UNSTABLE TRIPLET REPEAT IN A GENE-RELATED TO MYOTONIC MUSCULAR-DYSTROPHY BY FU,Y.H., PIZZUTI,A., FENWICK,R.G., ET-AL | 0 | 0 |
| 1360 | 7 | 10 | 1180 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):463-465 RYYNANEN M; PULKKINEN L; KIRKINEN P; SAARIKOSKI S FRAGILE-X SYNDROME IN EAST FINLAND - MOLECULAR APPROACH TO GENETIC AND PRENATAL-DIAGNOSIS | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1361 | 8 | 10 | 1185 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 |
| 1362 | 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 |
| 1363 | 9 | 10 | 1410 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):187-190 Grasso M; Perroni L; Colella S; Piombo G; Argusti A; Lituania M; Buscaglia M; Giussani U; Grimoldi MG; Bricarelli FD Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome | 1 | 2 |
| 1364 | 3 | 10 | 1524 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):227-231 Roge B Fragile X syndrome. Special education: the French context | 0 | 0 |
| 1365 | 6 | 10 | 1564 1997 ANNALS OF CLINICAL BIOCHEMISTRY 34:517-520 Chen TA; Lu XF; Che PK; Ho WKK Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects | 5 | 7 |
| 1366 | 8 | 10 | 1574 1997 BRITISH MEDICAL JOURNAL 315(7117):1223-1226 Turner G; Robinson H; Wake S; Laing S; Partington M Case finding for the fragile X syndrome and its consequences | 5 | 9 |
| 1367 | 7 | 10 | 1608 1997 JOURNAL OF MEDICAL GENETICS 34(3):250-251 Willemsen R; Los F; Mohkamsing S; vandenOuweland A; Deelen W; Galjaard H; Oostra B Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A new appraisal | 10 | 12 |
| 1368 | 3 | 10 | 1623 1997 PEDIATRICS 99(5):753-753 Hagerman R Fragile X: Treatment of hyperactivity | 0 | 1 |
| 1369 | 4 | 10 | 1630 1997 SOUTH AFRICAN MEDICAL JOURNAL 87(4):418-420 Goldman A; Krause A; Jenkins T Fragile X syndrome occurs in the South African black population | 2 | 4 |
| 1370 | 8 | 10 | 1643 1998 CLINICAL GENETICS 53(3):200-201 Mornet E; Chateau C; Simon-Bouy B; Serre JL The intermediate alleles of the fragile X CGG repeat in patients with mental retardation | 3 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1371 | 0 | 10 | 1658 1998 GENERAL HOSPITAL PSYCHIATRY 20(2):126-127 Silva JA; Ferrari MM; Leong GB Erotomania in a case of fragile-X syndrome | 0 | 1 |
| 1372 | 5 | 10 | 1789 1999 HEREDITAS 130(2):189-190 Sucharov CC; Silva R; Rondinelli E; Moura-Neto RS Fragile X trinucleotide repeats from a normal population in Rio de Janeiro, Brazil | 0 | 0 |
| 1373 | 8 | 10 | 1800 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:47-53 Carmichael B; Pembrey M; Turner G; Barnicoat A Diagnosis of fragile-X syndrome: the experiences of parents | 9 | 11 |
| 1374 | 5 | 10 | 1889 2000 GENETIC TESTING 4(3):241-242 Brown WT; Nolin SL Apparent FMR1 allele instability in non-Fragile X males - Invited commentary | 0 | 1 |
| 1375 | 7 | 10 | 1960 2000 PEDIATRIC HEMATOLOGY AND ONCOLOGY 17(7):597-600 Ferrari A; Meazza C; Casanova M Nasopharyngeal carcinoma in a boy with fragile X syndrome | 0 | 0 |
| 1376 | 1 | 10 | 1964 2000 VETERINARNI MEDICINA 45(10-11):308-310 Slota E; Danielak-Czech B; Pietraszewska J; Kozubska-Sobocinska A Preliminary identification of the fragile X in two crossbred cows | 0 | 1 |
| 1377 | 3 | 10 | 2047 2001 NEUROLOGY 57(1):127-130 Hagerman RJ; Leehey M; Heinrichs W; Tassone F; Wilson R; Hills J; Grigsby J; Gage B; Hagerman PJ Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 29 | 45 |
| 1378 | 0 | 10 | 2190 2002 PANMINERVA MEDICA 44(1):7-10 Bargagna S; Canepa G; Tinelli F Social adjustment in children with Down mental retardation (MRD) and Fragile-X mental retardation (MRX) | 0 | 1 |
| 1379 | 8 | 10 | 2288 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(3):372-375 Lombroso PJ Genetics of childhood disorders: XLVIII. Learning and memory, part 1: Fragile X syndrome update | 0 | 0 |
| 1380 | 7 | 10 | 2295 2003 NEURON 38(6):843-845 Billuart P; Chelly J From fragile X mental retardation protein to Rac1 GTPase: New insights from fly CYFIP | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1381 | 4 | 10 | 2310 2004 ACTA PHARMACOLOGICA SINICA 25(7):973-976 Sun YJ; Han X Dynamic behavior of fragile X full mutations in cultured female fetal fibroblasts | 0 | 0 |
| 1382 | 0 | 9 | 23 1981 LANCET 1(8219):556-557 SOUDEK D; MCGREGOR T SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 6 | 9 |
| 1383 | 0 | 9 | 24 1981 LANCET 1(8219):557-557 EBERLE G; ZANKL H; ZANKL M SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 4 | 8 |
| 1384 | 4 | 9 | 77 1982 LANCET 1(8266):273-274 LEJEUNE J IS THE FRAGILE-X SYNDROME AMENABLE TO TREATMENT | 46 | 61 |
| 1385 | 3 | 9 | 137 1983 HUMAN GENETICS 65(1):88-89 SOUDEK D; EMANUEL M A FRAGILE X SUPPRESSOR IN THE NORMAL HUMAN-BLOOD | 3 | 4 |
| 1386 | 3 | 9 | 146 1983 JOURNAL OF MEDICAL GENETICS 20(4):314-315 HUNTER AGW; MACDONALD J; EVANS JA ABSENCE OF THE FRAGILE-X IN A GROUP OF PATIENTS WITH IDIOPATHIC MENTAL-RETARDATION | 0 | 0 |
| 1387 | 1 | 9 | 150 1983 LANCET 1(8335):1221-1222 RUDELLI RD; JENKINS EC; WISNIEWSKI K; MORETZ R; BYRNE J; BROWN WT TESTICULAR SIZE IN FETAL FRAGILE X SYNDROME | 14 | 19 |
| 1388 | 3 | 9 | 183 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):299-301 ERBE RW FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 4 | 8 |
| 1389 | 1 | 9 | 192 1984 CLINICAL GENETICS 25(2):135-139 GARDINER GB; WENGER SL; STEELE MW INVITRO REVERSAL OF FRAGILE-X EXPRESSION BY EXOGENOUS THYMIDINE | 5 | 7 |
| 1390 | 0 | 9 | 201 1984 HUMAN GENETICS 65(4):400-401 FRYNS JP; KLECZKOWSKA A; KUBIEN E; PETIT P; VANDENBERGHE H INACTIVATION PATTERN OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 18 | 27 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1391 | 1 | 9 | 282 1985 HUMAN GENETICS 69(3):206-208 MAYER M; ABRUZZO MA; JACOBS PA; YEE SC A CYTOGENETIC STUDY OF A POPULATION OF RETARDED FEMALES WITH SPECIAL REFERENCE TO THE FRAGILE (X) SYNDROME | 4 | 10 |
| 1392 | 2 | 9 | 382 1986 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 28(5):624-627 GILLBERG C; WAHLSTROM J; JOHANSSON R; TORNBLOM M; ALBERTSSONWIKLAND K FOLIC-ACID AS AN ADJUNCT IN THE TREATMENT OF CHILDREN WITH THE AUTISM FRAGILE-X SYNDROME (AFRAX) | 6 | 15 |
| 1393 | 6 | 9 | 448 1987 GENETIKA 23(3):504-509 SULEIMANOVA DG; KULESHOV NP SPONTANEOUS AND INDUCED CHROMOSOMAL INSTABILITY IN PATIENTS WITH FRAGILE X-CHROMOSOME, SUFFERING FROM X-LINKED MENTAL-RETARDATION | 1 | 3 |
| 1394 | 4 | 9 | 513 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):109-113 FRYNS JP; VANDENBERGHE H THE CONCURRENCE OF KLINEFELTER SYNDROME AND FRAGILE-X SYNDROME | 14 | 17 |
| 1395 | 3 | 9 | 516 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):143-147 NIELSEN KB GROWTH-PATTERN IN BOYS WITH FRAGILE-X | 3 | 3 |
| 1396 | 5 | 9 | 607 1988 NEUROTOXICOLOGY 9(3):359-365 EDWARDS DR; KEPPEN LD; RANELLS JD; GOLLIN SM AUTISM IN ASSOCIATION WITH FRAGILE X-SYNDROME IN FEMALES - IMPLICATIONS FOR DIAGNOSIS AND TREATMENT IN CHILDREN | 4 | 7 |
| 1397 | 4 | 9 | 628 1989 BRITISH HEART JOURNAL 61(3):289-291 SREERAM N; WREN C; BHATE M; ROBERTSON P; HUNTER S CARDIAC ABNORMALITIES IN THE FRAGILE X-SYNDROME | 6 | 9 |
| 1398 | 4 | 9 | 648 1989 JOURNAL OF MEDICAL GENETICS 26(7):439-442 VOULLAIRE LE; WEBB GC; LEVERSHA M FRAGILE X-TESTING IN A DIAGNOSTIC CYTOGENETICS LABORATORY | 3 | 7 |
| 1399 | 2 | 9 | 790 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):305-310 MURPHY PD; WATSON MS; SHAPIRO LR; WILMOT PL; BREG WR DNA-BASED GENETIC TESTING IN 50 FRAGILE-X FAMILIES | 2 | 2 |
| 1400 | 3 | 9 | 824 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):509-509 HECHT F SEIZURE DISORDERS IN THE FRAGILE-X CHROMOSOME SYNDROME | 3 | 7 |
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