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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by journal name.
Page 9: 1 2 3 4 5 6 7 8 9
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2401 | 1 | 6 | 83 1982 NEW ENGLAND JOURNAL OF MEDICINE 306(25):1551-1552 POPOVICH B; VEKEMANS M; ROSENBLATT D; MONROE P FRAGILE-X | 17 | 21 |
| 2402 | 2 | 6 | 157 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(5):285-286 HECHT F; GLOVER TW ANTIBIOTICS CONTAINING TRIMETHOPRIM AND THE FRAGILE X-CHROMOSOME | 4 | 6 |
| 2403 | 2 | 6 | 158 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(23):1424-1424 HAGERMAN RJ; LEVITAS A DILANTIN AND THE FRAGILE X-SYNDROME | 0 | 2 |
| 2404 | 6 | 11 | 228 1984 NEW ENGLAND JOURNAL OF MEDICINE 310(22):1462-1462 WATSON MS; LECKMAN JF; ANNEX B; BREG WR; BOLES D; et al. FRAGILE X IN A SURVEY OF 75 AUTISTIC MALES | 34 | 56 |
| 2405 | 0 | 1 | 229 1984 NEW ENGLAND JOURNAL OF MEDICINE 310(22):1471-1471 STEIN M THE FRAGILE X SYNDROME - DIAGNOSIS, BIOCHEMISTRY, AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 2406 | 1 | 6 | 408 1986 NEW ENGLAND JOURNAL OF MEDICINE 315(10):607-609 TURNER G; ROBINSON H; LAING S; PURVISSMITH S PREVENTIVE SCREENING FOR THE FRAGILE-X SYNDROME | 99 | 126 |
| 2407 | 0 | 1 | 489 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 TURNER G THE FRAGILE X-CHROMOSOME - REPLY | 1 | 1 |
| 2408 | 0 | 0 | 490 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 HECHT F; HECHT BK THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 2409 | 4 | 4 | 491 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 BURD L THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 2410 | 15 | 28 | 892 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1673-1681 ROUSSEAU F; HEITZ D; BIANCALANA V; BLUMENFELD S; KRETZ C; et al. DIRECT DIAGNOSIS BY DNA ANALYSIS OF THE FRAGILE X-SYNDROME OF MENTAL-RETARDATION | 290 | 445 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2411 | 6 | 11 | 893 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1720-1722 SUTHERLAND GR; GEDEON A; KORNMAN L; DONNELLY A; BYARD RW; et al. PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT DETECTION OF THE UNSTABLE DNA-SEQUENCE | 62 | 86 |
| 2412 | 7 | 11 | 894 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1736-1738 SHAPIRO LR THE FRAGILE X-SYNDROME - A PECULIAR PATTERN OF INHERITANCE | 2 | 5 |
| 2413 | 0 | 1 | 1 1967 NEW PHYTOLOGIST 66(1):138-& CORNER EJH VANSTEENIS,CGG - PACIFIC PLANT AREAS 2 | 0 | 0 |
| 2414 | 0 | 0 | 1428 1995 NEW SCIENTIST 147(1985):10-10 WEBB J QUESTION MARK HANGS OVER FRAGILE-X TEST IN NEWBORNS | 0 | 0 |
| 2415 | 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 |
| 2416 | 13 | 45 | 1565 1996 NIMHANS JOURNAL 14(3):201-207 Suresh KP; Girimaji SR; Manjunatha KR Newer genetics in mental retardation .1. Fragile X syndrome and triplet repeat mutations | 0 | 1 |
| 2417 | 0 | 4 | 663 1989 NUCLEIC ACIDS RESEARCH 17(24):10513-10513 GRUNDY C; CHITOLIE A; TALBOT S; BEVAN D; KAKKAR V; et al. PROTEIN-C LONDON .1. RECURRENT MUTATION AT ARG-169 (CGG-]TGG) IN THE PROTEIN-C GENE CAUSING THROMBOSIS | 0 | 19 |
| 2418 | 1 | 1 | 729 1990 NUCLEIC ACIDS RESEARCH 18(3):690-690 YU S; SUTHERS GK; MULLEY JC A BCLI RFLP FOR DXS296 (VK21) NEAR THE FRAGILE-X | 2 | 6 |
| 2419 | 0 | 2 | 730 1990 NUCLEIC ACIDS RESEARCH 18(3):692-692 HUPKES PE; VANBENNEKOM CA; VANOOST BA; OOSTRA BA RN1, A NEW POLYMORPHIC MARKER NEAR THE FRAGILE-X LOCUS - (HGM10 ASSIGNMENT DXS-369) | 1 | 2 |
| 2420 | 0 | 3 | 731 1990 NUCLEIC ACIDS RESEARCH 18(20):6134-6134 WEILL D; HEYMAN T NUCLEOTIDE-SEQUENCE OF 2 PROLINE TRANSFER-RNA (AGG AND CGG) GENES FROM CHICKEN | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2421 | 10 | 25 | 895 1991 NUCLEIC ACIDS RESEARCH 19(10):2567-2572 DIETRICH A; KIOSCHIS P; MONACO AP; GROSS B; KORN B; et al. MOLECULAR-CLONING AND ANALYSIS OF THE FRAGILE X-REGION IN MAN | 23 | 45 |
| 2422 | 9 | 25 | 896 1991 NUCLEIC ACIDS RESEARCH 19(12):3283-3288 HIRST MC; RACK K; NAKAHORI Y; ROCHE A; BELL MV; et al. A YAC CONTIG ACROSS THE FRAGILE X SITE DEFINES THE REGION OF FRAGILITY | 16 | 42 |
| 2423 | 10 | 20 | 897 1991 NUCLEIC ACIDS RESEARCH 19(16):4355-4359 NAKAHORI Y; KNIGHT SJL; HOLLAND J; SCHWARTZ C; ROCHE A; et al. MOLECULAR HETEROGENEITY OF THE FRAGILE-X SYNDROME | 61 | 91 |
| 2424 | 0 | 2 | 1019 1992 NUCLEIC ACIDS RESEARCH 20(4):928-928 BHATIA K; GUTIERREZ MI; HUPPI K; MAGRATH IT PCR DETECTION OF A NEUTRAL CGA/CGG DIMORPHISM IN EXON-6 OF THE HUMAN P53 GENE | 0 | 21 |
| 2425 | 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 |
| 2426 | 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 |
| 2427 | 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 |
| 2428 | 5 | 27 | 1566 1996 NUCLEIC ACIDS RESEARCH 24(4):784-792 Mariappan SVS; Catasti P; Chen X; Ratliff R; Moyzis RK; et al. Solution structures of the individual single strands of the fragile X DNA triplets (GCC)(n)center dot(GGC)(n) | 12 | 49 |
| 2429 | 17 | 31 | 1700 1997 NUCLEIC ACIDS RESEARCH 25(14):2883-2887 Sandberg G; Schalling M Effect of in vitro promoter methylation and CGG repeat expansion on FMR-1 expression | 10 | 24 |
| 2430 | 0 | 35 | 1701 1997 NUCLEIC ACIDS RESEARCH 25(15):3042-3050 Vuidepot AL; Bontems F; Gervais M; Guiard B; Shechter E; et al. NMR analysis of CYP1(HAP1) DNA binding domain - CYC1 upstream activation sequence interactions: recognition of a CGG trinucleotide and of an additional thymine 5 bp downstream by the zinc cluster and the N-terminal extremity of the protein | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2431 | 0 | 26 | 1793 1998 NUCLEIC ACIDS RESEARCH 26(12):3001-3005 Dutta R; Gao YG; Priebe W; Wang AHJ Binding of the modified daunorubicin WP401 adjacent to a T-G base pair induces the reverse Watson-Crick conformation: crystal structures of the WP401-TGGCCG and WP401-CGG[br(5)C]CG complexes | 0 | 5 |
| 2432 | 32 | 45 | 2085 2000 NUCLEIC ACIDS RESEARCH 28(7):1535-1541 Weisman-Shomer P; Cohen E; Fry M Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures | 6 | 11 |
| 2433 | 14 | 42 | 2086 2000 NUCLEIC ACIDS RESEARCH 28(10):2141-2152 Genc B; Muller-Hartmann H; Zeschnigk M; Deissler H; Schmitz B; et al. Methylation mosaicism of 5 '-(CGG)(n)-3 ' repeats in fragile X, premutation and normal individuals | 3 | 6 |
| 2434 | 20 | 36 | 2190 2001 NUCLEIC ACIDS RESEARCH 29(11):2276-2283 Li ZZ; Zhang YY; Ku L; Wilkinson KD; Warren ST; et al. The fragile X mental retardation protein inhibits translation via interacting with mRNA | 72 | 93 |
| 2435 | 6 | 47 | 2191 2001 NUCLEIC ACIDS RESEARCH 29(22):4684-4690 Fojtik P; Vorlickova M The fragile X chromosome (GCC) repeat folds into a DNA tetraplex at neutral pH | 0 | 1 |
| 2436 | 19 | 36 | 2334 2002 NUCLEIC ACIDS RESEARCH 30(14):3278-3285 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; et al. Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 3 | 9 |
| 2437 | 8 | 58 | 2335 2002 NUCLEIC ACIDS RESEARCH 30(17):3672-3681 Weisman-Shomer P; Cohen E; Fry M Distinct domains in the CArG-box binding factor A destabilize tetraplex forms of the fragile X expanded sequence d(CGG)(n) | 2 | 3 |
| 2438 | 21 | 50 | 2468 2003 NUCLEIC ACIDS RESEARCH 31(14):3963-3970 Weisman-Shomer P; Cohen E; Hershco I; Khateb S; Wolfovitz-Barchad O; et al. The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)(n) | 3 | 5 |
| 2439 | 10 | 23 | 2469 2003 NUCLEIC ACIDS RESEARCH 31(21):6243-6248 Handa V; Saha T; Usdin K The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer | 3 | 7 |
| 2440 | 17 | 41 | 2602 2004 NUCLEIC ACIDS RESEARCH 32(1):298-306 Fojtik P; Kejnovska I; Vorlickova M The guanine-rich fragile X chromosome repeats are reluctant to form tetraplexes | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2441 | 24 | 40 | 2603 2004 NUCLEIC ACIDS RESEARCH 32(7):2129-2137 Gabus C; Mazroui R; Tremblay S; Khandjian EW; Darlix JL The fragile X mental retardation protein has nucleic acid chaperone properties | 2 | 5 |
| 2442 | 18 | 44 | 2604 2004 NUCLEIC ACIDS RESEARCH 32(14):4145-4154 Khateb S; Weisman-Shomer P; Hershco I; Loeb LA; Fry M Destabilization of tetraplex structures of the fragile X repeat sequence (CGG)(n) is mediated by homolog-conserved domains in three members of the hnRNP family | 0 | 0 |
| 2443 | 24 | 45 | 2645 2005 NUCLEIC ACIDS RESEARCH 33(2):451-463 Napierala M; Michalowski D; de Mezer M; Krzyzosiak WJ Facile FMR1 mRNA structure regulation by interruptions in CGG repeats | 0 | 0 |
| 2444 | 3 | 11 | 230 1984 OBSTETRICS AND GYNECOLOGY 63(3):S19-S21 HOGGE WA; SCHONBERG SA; GLOVER TW; HECHT F; GOLBUS MS PRENATAL-DIAGNOSIS OF FRAGILE (X) SYNDROME | 7 | 14 |
| 2445 | 27 | 80 | 2336 2002 OBSTETRICS AND GYNECOLOGY CLINICS OF NORTH AMERICA 29(2):367-+ Wenstrom KD Fragile X and other trinucleotide repeat diseases | 1 | 3 |
| 2446 | 0 | 0 | 2337 2002 ONKOLOGIE 25(5):482-483 Diel I; Chatsiproios D Concept of integrated gyneco-oncological care: Centrum fur ganzheitliche gynakologie (CGG Klinik GmbH) | 0 | 0 |
| 2447 | 0 | 0 | 898 1991 OPTOMETRY AND VISION SCIENCE 68(8):634-640 MAINO DM; WESSON M; SCHLANGE D; CIBIS G; MAINO JH OPTOMETRIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 2448 | 19 | 33 | 1794 1998 OPTOMETRY AND VISION SCIENCE 75(12):856-859 Kranjc BS; Brezigar A; Peterlin B Bilateral macular dysplasia in fragile X syndrome | 0 | 0 |
| 2449 | 33 | 54 | 2087 2000 OPTOMETRY AND VISION SCIENCE 77(11):592-599 Block SS; Brusca-Vega R; Pizzi WJ; Berry-Kravis E; Maino DM; et al. Cognitive and visual processing skills and their relationship to mutation size in full and premutation female fragile X carriers | 0 | 0 |
| 2450 | 0 | 10 | 2338 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2451 | 7 | 11 | 732 1990 PATHOBIOLOGY 58(4):236-240 JENKINS EC; DUNCAN CJ; SANZ MM; GENOVESE M; GU H; et al. PROGRESS TOWARD AN INTERNAL CONTROL-SYSTEM FOR FRAGILE-X INDUCTION BY 5-FLUORODEOXYURIDINE IN WHOLE-BLOOD CULTURES | 3 | 6 |
| 2452 | 0 | 0 | 159 1983 PATHOLOGY 15(1):105-106 JACKY PB; SUTHERLAND GR FRAGILE-X EXPRESSION IN FIBROBLASTS | 0 | 0 |
| 2453 | 0 | 0 | 231 1984 PATHOLOGY 16(1):108-108 SUTHERLAND GR THE FRAGILE X-CHROMOSOME | 0 | 0 |
| 2454 | 0 | 0 | 232 1984 PATHOLOGY 16(1):108-108 THEOBALD TM; HAY DA INDIVIDUAL VARIATION AND SPECIFIC COGNITIVE DEFICITS IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 2455 | 7 | 10 | 2088 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 |
| 2456 | 0 | 0 | 492 1987 PEDIATRIC NEUROLOGY 3(5):284-287 MATSUISHI T; SHIOTSUKI Y; NIIKAWA N; KATAFUCHI Y; OTAKI E; et al. FRAGILE-X SYNDROME IN JAPANESE PATIENTS WITH INFANTILE-AUTISM | 4 | 6 |
| 2457 | 18 | 33 | 1020 1992 PEDIATRIC NEUROLOGY 8(4):272-274 WONG VCN; LAM STS FRAGILE X POSITIVITY IN CHINESE CHILDREN WITH AUTISTIC SPECTRUM DISORDER | 3 | 5 |
| 2458 | 12 | 14 | 1567 1996 PEDIATRIC NEUROLOGY 15(4):358-360 Kluger G; Bohm I; Laub MC; Waldenmaier C Epilepsy and fragile X gene mutations | 6 | 12 |
| 2459 | 0 | 0 | 34 1981 PEDIATRIC RESEARCH 15(4):560-560 CARPENTER NJ; LEICHTMAN LG; SAY B STUDIES ON THE FRAGILE X-SYNDROME IN SUBJECTS WITH MENTAL-RETARDATION OF UNKNOWN ETIOLOGY | 0 | 0 |
| 2460 | 0 | 0 | 35 1981 PEDIATRIC RESEARCH 15(4):569-569 SHAPIRO LR; KUHR MD; WILMOT PL MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2461 | 0 | 0 | 36 1981 PEDIATRIC RESEARCH 15(4):645-645 PUESCHEL SM; HAYS R; MENDOZA T A FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MULTIPLE CONGENITAL-ANOMALIES, MEGALOGENITALIA AND A FRAGILE X-CHROMOSOME | 1 | 1 |
| 2462 | 0 | 0 | 310 1985 PEDIATRIC RESEARCH 19(4):A253-A253 ROSENBLATT DS; ZEESMAN SF; VEKEMANS MJJ; DUSCHENES EA; HELLSTROM FV; et al. FOLIC-ACID BLINDED TRIAL IN IDENTICAL-TWINS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 2463 | 0 | 0 | 409 1986 PEDIATRIC RESEARCH 20(4):A269-A269 MURPHY PD; WATSON MS; KIDD KK; BREG WR MOLECULAR APPROACHES TO CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME (MCKUSICK NUMBER 30920) | 1 | 2 |
| 2464 | 0 | 0 | 410 1986 PEDIATRIC RESEARCH 20(4):A273-A273 WENGER SL; HENNESSEY JC; STEELE MW INCREASED SISTER CHROMATID EXCHANGE (SCE) AT THE FRAGILE X-SITE IN AFFECTED MALES | 0 | 0 |
| 2465 | 0 | 0 | 493 1987 PEDIATRIC RESEARCH 21(4):A230-A230 SHAPIRO LR; WILMOT PL; OMAR RA; DAVIDIAN MM; CHANDER PN PRENATAL PATHOGENESIS OF MACROORCHIDISM IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 2466 | 0 | 0 | 664 1989 PEDIATRIC RESEARCH 25(4):A16-A16 MERYASH DL PERCEPTION OF BURDEN AMONG AT-RISK WOMEN OF RAISING A CHILD WITH FRAGILE-X SYNDROME | 0 | 0 |
| 2467 | 0 | 0 | 733 1990 PEDIATRIC RESEARCH 27(4):A12-A12 LACHIEWICZ AM; SPIRIDIGLIOZZI GA; GULLION CA; RANSFORD SK ABERRANT BEHAVIORS OF YOUNG BOYS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 2468 | 0 | 0 | 734 1990 PEDIATRIC RESEARCH 27(4):A136-A136 SHAPIRO LR; WILMOT PL SPONTANEOUS FRAGILE-X CHROMOSOMES IN ROUTINE AMNIOTIC-FLUID CULTURE - THE X-CHROMOSOME COMMON FRAGILE SITE [(X) (Q27.2)] MISTAKEN FOR THE FRAGILE-X CHROMOSOME [(X) (Q27.3)] | 0 | 0 |
| 2469 | 0 | 0 | 899 1991 PEDIATRIC RESEARCH 29(4):A134-A134 SHAPIRO LR; EALLONARDO SJ; WILMOT PL OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION AND THE FRAGILE-X SYNDROME | 0 | 0 |
| 2470 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2471 | 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 |
| 2472 | 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 |
| 2473 | 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 |
| 2474 | 0 | 0 | 1568 1996 PEDIATRIC RESEARCH 39(2):371-371 Torrado M; Herrera J; Chertkoff L; Tenembaum S; Bin L; et al. Diagnosis value of a pediatric clinical score for the diagnosis of the Fragile X Syndrome | 0 | 0 |
| 2475 | 1 | 15 | 37 1981 PEDIATRICS 68(4):594-595 GERALD PS X-LINKED MENTAL-RETARDATION AND THE FRAGILE-X SYNDROME | 5 | 11 |
| 2476 | 1 | 7 | 84 1982 PEDIATRICS 69(5):668-669 RHOADS FA X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME | 11 | 12 |
| 2477 | 0 | 0 | 85 1982 PEDIATRICS 69(5):669-669 GERALD PS X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME - REPLY | 1 | 1 |
| 2478 | 0 | 0 | 86 1982 PEDIATRICS 69(5):670-670 HARPEY JP TREATMENT OF FRAGILE-X | 19 | 24 |
| 2479 | 3 | 23 | 233 1984 PEDIATRICS 74(5):883-886 CARMI R; MERYASH DL; WOOD J; GERALD PS FRAGILE-X SYNDROME ASCERTAINED BY THE PRESENCE OF MACRO-ORCHIDISM IN A 5-MONTH-OLD INFANT | 4 | 6 |
| 2480 | 8 | 19 | 665 1989 PEDIATRICS 83(4):547-552 SIMKO A; HORNSTEIN L; SOUKUP S; BAGAMERY N FRAGILE X-SYNDROME - RECOGNITION IN YOUNG-CHILDREN | 28 | 31 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2481 | 21 | 31 | 1021 1992 PEDIATRICS 89(3):395-400 HAGERMAN RJ; JACKSON C; AMIRI K; SILVERMAN AC; OCONNOR R; et al. GIRLS WITH FRAGILE-X SYNDROME - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 58 | 81 |
| 2482 | 10 | 23 | 1022 1992 PEDIATRICS 89(6):1059-1062 BUTLER MG; BRUNSCHWIG A; MILLER LK; HAGERMAN RJ STANDARDS FOR SELECTED ANTHROPOMETRIC MEASUREMENTS IN MALES WITH THE FRAGILE X-SYNDROME | 25 | 29 |
| 2483 | 20 | 37 | 1161 1993 PEDIATRICS 91(2):321-329 FREUND LS; REISS AL; ABRAMS MT PSYCHIATRIC-DISORDERS ASSOCIATED WITH FRAGILE-X IN THE YOUNG FEMALE | 58 | 80 |
| 2484 | 6 | 13 | 1162 1993 PEDIATRICS 91(4):714-715 CRABBE LS; BENSKY AS; HORNSTEIN L; SCHWARTZ DC CARDIOVASCULAR-ABNORMALITIES IN CHILDREN WITH FRAGILE-X SYNDROME | 5 | 7 |
| 2485 | 14 | 31 | 1280 1994 PEDIATRICS 93(6):992-995 LACHIEWICZ AM; DAWSON DV DO YOUNG BOYS WITH FRAGILE-X-SYNDROME HAVE MACROORCHIDISM | 13 | 17 |
| 2486 | 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 |
| 2487 | 24 | 29 | 1569 1996 PEDIATRICS 97(1):122-126 Hagerman RJ; Staley LW; OConner R; Lugenbeel K; Nelson D; et al. Learning-disabled males with a fragile X CGG expansion in the upper premutation size range | 29 | 40 |
| 2488 | 14 | 17 | 1570 1996 PEDIATRICS 98(2):297-300 Desposito F; Cho S; Frias JL; Sherman J; Wappner RS; et al. Health supervision for children with fragile X syndrome | 3 | 8 |
| 2489 | 3 | 10 | 1702 1997 PEDIATRICS 99(5):753-753 Hagerman R Fragile X: Treatment of hyperactivity | 0 | 1 |
| 2490 | 25 | 40 | 2192 2001 PEDIATRICS 108(5):art. no.-e88 Hessl D; Dyer-Friedman J; Glaser B; Wisbeck J; Barajas RG; et al. The influence of environmental and genetic factors on behavior problems and autistic symptoms in boys and girls with fragile X syndrome | 0 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2491 | 13 | 27 | 2339 2002 PEDIATRICS 109(1) Flynn BJ; Myers SM; Cera PJ; Mowad JJ Testicular torsion in an adolescent with fragile X syndrome | 0 | 0 |
| 2492 | 8 | 36 | 2470 2003 PEDIATRICS 111(2):407-416 Bailey DB; Skinner D; Sparkman KL Discovering fragile X syndrome: Family experiences and perceptions | 5 | 6 |
| 2493 | 0 | 0 | 160 1983 PEDIATRIE 38(3):191-198 JALBERT P FRAGILE X-LINKED MENTAL-RETARDATION - MORE QUESTIONS | 1 | 3 |
| 2494 | 0 | 0 | 1023 1992 PEDIATRIE 47(11):743-750 PELLISSIER MC; VOELCKEL MA; MATTEI JF FRAGILE-X SYNDROME - CURRENT KNOWLEDGE | 0 | 0 |
| 2495 | 0 | 6 | 1163 1993 PISMA V ZHURNAL TEKHNICHESKOI FIZIKI 19(14):43-48 KHAN VP; FEDOTOVA IV REPRESENTATION OF CGG (CHALCOGENIDE GLASSES) AS INORGANIC POLYMER AND POTENTIALITIES OF COMPUTATION OF EXCESSIVE HOMOBONDS FORMING IN THEM | 0 | 0 |
| 2496 | 0 | 0 | 494 1987 PRACTITIONER 231(1431):910-& BUNDEY S THE FRAGILE X-SYNDROME | 1 | 1 |
| 2497 | 0 | 0 | 735 1990 PRACTITIONER 234(1496):946-& BERNEY T FRAGILE-X SYNDROME | 0 | 0 |
| 2498 | 0 | 1 | 2605 2004 PRAXIS DER KINDERPSYCHOLOGIE UND KINDERPSYCHIATRIE 53(8):593-594 Irblich D The fragile X syndrome - A guide for parents | 0 | 0 |
| 2499 | 7 | 21 | 161 1983 PRENATAL DIAGNOSIS 3(2):131-137 WEBB T; GOSDEN CM; RODECK CH; HAMILL MA; EASON PE PRENATAL-DIAGNOSIS OF X-LINKED MENTAL-RETARDATION WITH FRAGILE (X) USING FETOSCOPY AND FETAL BLOOD-SAMPLING | 16 | 32 |
| 2500 | 3 | 8 | 162 1983 PRENATAL DIAGNOSIS 3(4):367-369 NIELSEN LB; NIELSEN KB; TOMMERUP N FRAGILE-X DEMONSTRATED RETROSPECTIVELY IN AMNIOTIC CELLS CULTURED IN LOW FOLATE MEDIUM | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2501 | 6 | 16 | 234 1984 PRENATAL DIAGNOSIS 4(1):61-66 WILSON MG; MARCHESE CA PRENATAL-DIAGNOSIS OF FRAGILE-X IN A HETEROZYGOUS FEMALE FETUS AND POSTNATAL FOLLOW-UP | 5 | 9 |
| 2502 | 3 | 6 | 235 1984 PRENATAL DIAGNOSIS 4(6):473-474 VENTER PA; COETZEE DJ; BADENHORST A; MARX MP; HOF JO; et al. A CONFIRMED PRENATAL-DIAGNOSIS OF A FEMALE FETUS WITH THE FRAGILE X-CHROMOSOME | 1 | 4 |
| 2503 | 2 | 7 | 311 1985 PRENATAL DIAGNOSIS 5(3):229-231 ROCCHI M; PECILE V; ARCHIDIACONO N; MONNI G; DUMEZ Y; et al. PRENATAL-DIAGNOSIS OF THE FRAGILE-X IN MALE MONOZYGOTIC TWINS - DISCORDANT EXPRESSION OF THE FRAGILE SITE IN AMNIOCYTES | 5 | 10 |
| 2504 | 4 | 7 | 495 1987 PRENATAL DIAGNOSIS 7(3):197-202 SUTHERLAND GR; BAKER E; PURVISSMITH S; HOCKEY A; KRUMINS E; et al. PRENATAL-DIAGNOSIS OF THE FRAGILE-X USING THYMIDINE INDUCTION | 5 | 13 |
| 2505 | 12 | 22 | 496 1987 PRENATAL DIAGNOSIS 7(3):203-214 WEBB TP; RODECK CH; NICOLAIDES KH; GOSDEN CM PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME USING FETAL BLOOD AND AMNIOTIC-FLUID | 9 | 18 |
| 2506 | 3 | 3 | 666 1989 PRENATAL DIAGNOSIS 9(11):777-781 WEBB TP; BUNDEY S; MCKINLEY M MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 3 | 5 |
| 2507 | 2 | 3 | 736 1990 PRENATAL DIAGNOSIS 10(8):545-546 OOSTRA BA; SANDKUYL LA; HALLEY DJJ RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 1 | 1 |
| 2508 | 0 | 0 | 737 1990 PRENATAL DIAGNOSIS 10(8):546-546 WEBB TP RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 2509 | 11 | 23 | 900 1991 PRENATAL DIAGNOSIS 11(5):333-338 WEBB T EXPRESSION OF FRAGILE-X IN A FEMALE FETUS DIAGNOSED AFTER CHORIONIC VILLUS SAMPLING | 3 | 4 |
| 2510 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2511 | 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 |
| 2512 | 35 | 63 | 1571 1996 PRENATAL DIAGNOSIS 16(13):1199-1211 Sutherland GR; Mulley JC Fragile X syndrome and Fragile XE mental retardation | 3 | 9 |
| 2513 | 14 | 23 | 1932 1999 PRENATAL DIAGNOSIS 19(13):1223-1230 Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; et al. Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG | 2 | 26 |
| 2514 | 10 | 17 | 2089 2000 PRENATAL DIAGNOSIS 20(8):611-614 Pesso R; Berkenstadt H; Cuckle H; Gak E; Peleg L; et al. Screening for fragile X syndrome in women of reproductive age | 13 | 17 |
| 2515 | 3 | 6 | 2090 2000 PRENATAL DIAGNOSIS 20(10):854-855 Wilkin H; Tuohy J; Theewis W Prenatal diagnosis of fragile X and Turner mosaicism in a 12-week fetus | 1 | 1 |
| 2516 | 13 | 31 | 2193 2001 PRENATAL DIAGNOSIS 21(6):504-511 Apessos A; Abou-Sleiman PM; Harper JC; Delhanty JDA Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers | 1 | 16 |
| 2517 | 18 | 22 | 2340 2002 PRENATAL DIAGNOSIS 22(6):459-462 Rife M; Mallolas J; Badenas C; Tazon B; Miguelez MR; et al. Pilot study for the neonatal screening of fragile X syndrome | 3 | 3 |
| 2518 | 24 | 41 | 2471 2003 PRENATAL DIAGNOSIS 23(4):345-351 Wald NJ; Morris JK A new approach to antenatal screening for Fragile X syndrome | 1 | 3 |
| 2519 | 1 | 1 | 2472 2003 PRENATAL DIAGNOSIS 23(9):771-771 Rife M; Mallolas J; Badenas C; Tazon B; Miguelez MR; et al. Pilot study for the neonatal screening of fragile X syndrome (vol 22, pg 459, 2002) | 0 | 0 |
| 2520 | 6 | 8 | 2606 2004 PRENATAL DIAGNOSIS 24(1):67-68 Delatycki MB; Sheffield LJ; Wake S; Cohen J Screening approach for Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2521 | 0 | 1 | 2607 2004 PRENATAL DIAGNOSIS 24(1):68-69 Wald NJ; Morris JK Reply: Prenatal screen for Fragile X syndrome | 0 | 0 |
| 2522 | 6 | 12 | 2608 2004 PRIMARY CARE 31(3):621-+ Wiesner GL; Cassidy SB; Grimes SJ; Matthews AL; Acheson LS Clinical consult: developmental delay/fragile X syndrome | 0 | 0 |
| 2523 | 10 | 29 | 411 1986 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 83(4):1016-1020 OBERLE I; HEILIG R; MOISAN JP; KLOEPFER C; MATTEI MG; et al. GENETIC-ANALYSIS OF THE FRAGILE-X MENTAL-RETARDATION SYNDROME WITH 2 FLANKING POLYMORPHIC DNA MARKERS | 41 | 65 |
| 2524 | 3 | 18 | 738 1990 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 87(10):3856-3860 WARREN ST; KNIGHT SJL; PETERS JF; STAYTON CL; CONSALEZ GG; et al. ISOLATION OF THE HUMAN CHROMOSOMAL BAND XQ28 WITHIN SOMATIC-CELL HYBRIDS BY FRAGILE X-SITE BREAKAGE | 24 | 69 |
| 2525 | 0 | 16 | 901 1991 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 88(3):921-925 OBA T; ANDACHI Y; MUTO A; OSAWA S CGG - AN UNASSIGNED OR NONSENSE CODON IN MYCOPLASMA-CAPRICOLUM | 1 | 49 |
| 2526 | 12 | 37 | 902 1991 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 88(19):8302-8306 POUSTKA A; DIETRICH A; LANGENSTEIN G; TONIOLO D; WARREN ST; et al. PHYSICAL MAP OF HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION | 7 | 75 |
| 2527 | 7 | 17 | 1024 1992 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 89(9):4215-4217 MORTON NE; MACPHERSON JN POPULATION-GENETICS OF THE FRAGILE-X SYNDROME - MULTIALLELIC MODEL FOR THE FMR1 LOCUS | 51 | 79 |
| 2528 | 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 |
| 2529 | 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 |
| 2530 | 24 | 69 | 1703 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(9):4587-4592 Hansen RS; Canfield TK; Fjeld AD; Mumm S; Laird CD; et al. A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication | 8 | 41 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2531 | 18 | 58 | 1704 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(10):5395-5400 Weiler IJ; Irwin SA; Klintsova AY; Spencer CM; Brazelton AD; et al. Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation | 102 | 192 |
| 2532 | 10 | 29 | 1705 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(10):5401-5404 Comery TA; Harris JB; Willems PJ; Oostra BA; Irwin SA; et al. Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits | 125 | 220 |
| 2533 | 10 | 36 | 2194 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98(13):7101-7106 Greenough WT; Klintsova AY; Irwin SA; Galvez R; Bates KE; et al. Synaptic regulation of protein synthesis and the fragile X protein | 42 | 63 |
| 2534 | 19 | 36 | 2195 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98(15):8844-8849 Schenck A; Bardoni B; Moro A; Bagni C; Mandel JL A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P | 27 | 51 |
| 2535 | 13 | 40 | 2341 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99(11):7746-7750 Huber KM; Gallagher SM; Warren ST; Bear MF Altered synaptic plasticity in a mouse model of fragile X mental retardation | 35 | 61 |
| 2536 | 23 | 52 | 2342 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99(24):15758-15763 Qin M; Kang J; Smith CB Increased rates of cerebral glucose metabolism in a mouse model of fragile X mental retardation | 5 | 6 |
| 2537 | 22 | 45 | 2473 2003 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 100(24):14374-14378 Todd PK; Mack KJ; Malter JS The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95 | 8 | 13 |
| 2538 | 14 | 57 | 2609 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(10):3615-3620 Menon V; Leroux J; White CD; Reiss AL Frontostriatal deficits in fragile X syndrome: Relation to FMR1 gene expression | 0 | 0 |
| 2539 | 26 | 61 | 2610 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(36):13357-13362 Khandjian EW; Huot ME; Tremblay S; Davidovic L; Mazroui R; et al. Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles | 6 | 7 |
| 2540 | 25 | 53 | 2611 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(42):15201-15206 Lu R; Wang HP; Liang Z; Ku L; O'Donnell WT; et al. The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2541 | 15 | 21 | 2612 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17329-17330 Miyashiro K; Eberwine J Fragile X syndrome: (What's) lost in translation? | 0 | 0 |
| 2542 | 18 | 61 | 2613 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17428-17433 Ling SC; Fahrner PS; Greenough WT; Gelfand VI Transport of Drosophila fragile X rental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein | 0 | 1 |
| 2543 | 28 | 50 | 2614 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17504-17509 Weiler IJ; Spangler CC; Klintsova AY; Grossman AW; Kim SH; et al. Fragile X mental retardation protein is necessary for neurotransmitter-activated protein translation at synapses | 0 | 0 |
| 2544 | 29 | 46 | 2646 2005 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 102(6):2180-2185 Aschrafi A; Cunningham BA; Edelman GM; Vanderklish PW The fragile X mental retardation protein and group I metabotropic glutamate receptors regulate levels of mRNA granules in brain | 0 | 0 |
| 2545 | 3 | 35 | 236 1984 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES 81(24):7855-7859 SZABO P; PURRELLO M; ROCCHI M; ARCHIDIACONO N; ALHADEFF B; et al. CYTOLOGICAL MAPPING OF THE HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE DISTAL TO THE FRAGILE-X SITE SUGGESTS A HIGH-RATE OF MEIOTIC RECOMBINATION ACROSS THIS SITE | 17 | 71 |
| 2546 | 0 | 21 | 2474 2003 PROTEIN EXPRESSION AND PURIFICATION 27(2):365-374 McNulty DE; Claffee BA; Huddleston MJ; Kane JF Mistranslational errors associated with the rare arginine codon CGG in Escherichia coli | 1 | 6 |
| 2547 | 1 | 1 | 2615 2004 PROTEIN EXPRESSION AND PURIFICATION 37(1):264-264 McNulty DE; Claffee BA; Huddleston MJ; Kane JF Mistranslational errors associated with the rare arginine codon CGG in Escherichia coli (vol 27, pg 365, 2003) | 0 | 0 |
| 2548 | 27 | 59 | 1025 1992 PSYCHIATRIC GENETICS 2(4):277-300 BOLTON P; PICKLES A; BUTLER L; SUMMERS D; WEBB T; et al. FRAGILE-X IN FAMILIES MULTIPLEX FOR AUTISM AND RELATED PHENOTYPES - PREVALENCE AND CRITERIA FOR CYTOGENETIC DIAGNOSIS | 1 | 7 |
| 2549 | 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 |
| 2550 | 16 | 28 | 1572 1996 PSYCHIATRIC GENETICS 6(2):81-86 Ashworth A; Abusaad I; Walsh C; Nanko S; Murray RM; et al. Linkage analysis of the fragile X gene FMR-1 and schizophrenia: No evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2551 | 23 | 44 | 1706 1997 PSYCHIATRIC GENETICS 7(3):115-119 ODwyer J; Holmes J; Mueller R; Taylor G The prevalence of Fragile-X syndrome in an institution for people with learning disability | 1 | 3 |
| 2552 | 23 | 46 | 1164 1993 PSYCHIATRIE DE L ENFANT 36(1):5-26 LIDAPULIK H; BASQUIN M COGNITIVE DISTURBANCES AND PSYCHIATRIC MANIFESTATIONS IN THE FRAGILE-X SYNDROME - AUTISM AND FRAGILE-X SYNDROME | 0 | 1 |
| 2553 | 8 | 27 | 1573 1996 PSYCHIATRY RESEARCH 64(2):97-104 Thompson NM; Rogeness GA; McClure E; Clayton R; Johnson C Influence of depression on cognitive functioning in Fragile X females | 1 | 6 |
| 2554 | 2 | 54 | 1707 1997 PSYCHIATRY RESEARCH-NEUROIMAGING 75(1):31-48 Kates WR; Abrams MT; Kaufmann WE; Breiter SN; Reiss AL Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome | 20 | 63 |
| 2555 | 21 | 41 | 667 1989 PSYCHOLOGY IN THE SCHOOLS 26(4):380-389 SIMENSEN RJ; ROGERS RC SCHOOL-PSYCHOLOGY AND MEDICAL DIAGNOSIS - THE FRAGILE X-SYNDROME | 1 | 1 |
| 2556 | 19 | 43 | 2343 2002 PSYCHONEUROENDOCRINOLOGY 27(7):855-872 Hessl D; Glaser B; Dyer-Friedman J; Blasey C; Hastie T; et al. Cortisol and behavior in fragile X syndrome | 6 | 9 |
| 2557 | 0 | 0 | 3 1979 PSYCHOPHYSIOLOGY 16(2):194-195 HOLZL R NON-INVASIVE MEASUREMENT OF GASTRIC-MOTILITY BY CONJOINT GASTROGRAPHY (CGG) - METHOD AND PSYCHO-PHYSIOLOGICAL APPLICATIONS | 0 | 0 |
| 2558 | 3 | 53 | 2616 2004 QUALITATIVE HEALTH RESEARCH 14(6):741-759 Medved MI; Brockmeier J Making sense of traumatic experiences: Telling your life with fragile X syndrome | 0 | 0 |
| 2559 | 27 | 63 | 612 1988 QUARTERLY JOURNAL OF MEDICINE 69(258):755-763 FROSTERISKENIUS U; PATTERSON MN; BELL MV; BLOOMFIELD J; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME | 1 | 1 |
| 2560 | 16 | 34 | 1026 1992 REMEDIAL AND SPECIAL EDUCATION 13(2):32-39 SANTOS KE FRAGILE X-SYNDROME - AN EDUCATORS ROLE IN IDENTIFICATION, PREVENTION, AND INTERVENTION | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2561 | 0 | 1 | 2617 2004 REPRODUCTIVE BIOMEDICINE ONLINE 8(3):337-337 [Anon] Late onset fragile X syndrome | 0 | 0 |
| 2562 | 0 | 0 | 668 1989 REVISTA BRASILEIRA DE GENETICA 12(2):391-404 NAVAJAS L; VIANNAMORGANTE AM RELATIONSHIP BETWEEN AGE AND MENTAL STATUS AND THE EXPRESSION OF THE FRAGILE(X) IN HETEROZYGOTES FOR THE MARTIN-BELL SYNDROME | 0 | 0 |
| 2563 | 31 | 49 | 1708 1997 REVISTA DE NEUROLOGIA 25(143):1068-1071 EstevezGonzalez A; Roig C; Piles S; Pineda M; GarciaSanchez C Fragile-X syndrome and mental retardation | 1 | 1 |
| 2564 | 1 | 5 | 2091 2000 REVISTA DE NEUROLOGIA 30(10):996-997 Serrano-Castro PJ; Serrano-Castillo P A historical description of the association of macro-orchidea, mental retardation and cranial dysmorphia in males (fragile X chromosome syndrome) by A.B Richerand | 0 | 0 |
| 2565 | 5 | 18 | 2196 2001 REVISTA DE NEUROLOGIA 33:S6-S9 Glover G; Bernabe MJ; Carbonell P Gnosis of fragile X syndrome | 0 | 0 |
| 2566 | 19 | 22 | 2197 2001 REVISTA DE NEUROLOGIA 33:S9-S13 Ramos-Fuentes FJ New methods for the diagnosis of fragile X syndrome: A study of the FMRP in blood and hair | 0 | 0 |
| 2567 | 21 | 30 | 2198 2001 REVISTA DE NEUROLOGIA 33:S14-S19 Tejada MI Prevention of fragile X syndrome by prenatal genetic diagnosis: Advantages and controversial aspects | 0 | 0 |
| 2568 | 8 | 25 | 2199 2001 REVISTA DE NEUROLOGIA 33:S20-S23 Mila M; Mallolas J Fragile X syndrome: Premature ovarian failure. Preimplantation and preconception genetic diagnosis | 0 | 0 |
| 2569 | 13 | 30 | 2200 2001 REVISTA DE NEUROLOGIA 33:S24-S29 Cornish K; Munir F; Wilding J A neuropsychological and behavioural profile of a attention deficits in fragile X syndrome | 2 | 2 |
| 2570 | 9 | 15 | 2201 2001 REVISTA DE NEUROLOGIA 33:S29-S32 Brun-Gasca C; Artigas-Pallares J Psycholinguistic aspects of fragile X chromosome syndrome | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2571 | 3 | 19 | 2202 2001 REVISTA DE NEUROLOGIA 33:S32-S36 Goldson E Sensory integration and fragile X syndrome | 0 | 0 |
| 2572 | 2 | 12 | 2203 2001 REVISTA DE NEUROLOGIA 33:S37-S41 Carrasco M Informing members of families affected by fragile X syndrome of this diagnosis | 0 | 0 |
| 2573 | 15 | 42 | 2204 2001 REVISTA DE NEUROLOGIA 33:S41-S50 Artigas-Pallares J; Brun-Gasca C Medical treatment of fragile X syndrome | 0 | 0 |
| 2574 | 63 | 105 | 2205 2001 REVISTA DE NEUROLOGIA 33:S51-S57 Hagerman RJ; Hagerman PJ Fragile X syndrome: A model of gene-brain-behaviour relationships | 0 | 0 |
| 2575 | 14 | 29 | 2206 2001 REVISTA DE NEUROLOGIA 33:S62-S65 Chiurazzi P; Neri G Experimental therapy: Reactivation of the FMR1 gene involved in fragile X syndrome | 0 | 0 |
| 2576 | 3 | 52 | 2207 2001 REVISTA DE NEUROLOGIA 33:S65-S70 Calvani M; D'Iddio S; de Gaetano A; Mariotti P; Mosconi L; et al. L-acetylcarnityne treatment on fragile X patients hyperactive behaviour | 0 | 0 |
| 2577 | 9 | 40 | 2208 2001 REVISTA DE NEUROLOGIA 33:S70-S76 de Diego-Otero Y Experimental therapeutic models for fragile X syndrome | 0 | 0 |
| 2578 | 0 | 7 | 2209 2001 REVISTA DE NEUROLOGIA 33:S77-S81 Safont-Tria NB Psychomotricity and fragile X syndrome | 0 | 0 |
| 2579 | 0 | 7 | 2210 2001 REVISTA DE NEUROLOGIA 33:S82-S87 Furgang R Language therapy in fragile X syndrome | 0 | 0 |
| 2580 | 0 | 0 | 2211 2001 REVISTA DE NEUROLOGIA 33:S88-S90 [Anon] Interdisciplinary conference on the fragile X syndrome - Barcelona, October 27-28, 2001 - Abstracts | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2581 | 2 | 7 | 2618 2004 REVISTA DE NEUROLOGIA 38(1):7-11 Artigas-Pallares J; Brun-Gasca C Can the behavioural phenotype of Fragile X syndrome be attributed to mental retardation and to attention deficit hyperactivity disorder? | 0 | 0 |
| 2582 | 6 | 26 | 163 1983 REVISTA MEDICA DE CHILE 111(6):597-600 SANTOS M; MORIZON G THE FRAGILE X SYNDROME - A CHROMOSOMAL DEFECT ASSOCIATED WITH MENTAL-RETARDATION | 0 | 0 |
| 2583 | 24 | 49 | 1574 1996 REVISTA MEDICA DE CHILE 124(7):865-872 Jara L; Avendano I; Aspillaga M; Blanco R Molecular and genetic features of fragile X syndrome. A review | 0 | 0 |
| 2584 | 30 | 41 | 1795 1998 REVISTA MEDICA DE CHILE 126(8):911-918 Jara L; Lopez M; Mellado C; Aspillaga M; Avendano I; et al. Clinical and metabolic screening for fragile X syndrome in 300 patients with unspecific mental retardation | 1 | 1 |
| 2585 | 10 | 25 | 1796 1998 REVISTA MEDICA DE CHILE 126(12):1447-1454 Aspillaga M; Jara L; Avendano I; Lopez M Fragile X syndrome. Clinical analysis of 300 Chilean patients with unspecific mental retardation | 1 | 1 |
| 2586 | 0 | 0 | 412 1986 RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS 12(4):442-444 DELGIUDICE E; POGGI V; SARTORIO R; CARROZZO R; ROMANO A; et al. THE FRAGILE X-SYNDROME | 0 | 0 |
| 2587 | 15 | 43 | 1933 1999 RNA-A PUBLICATION OF THE RNA SOCIETY 5(9):1248-1258 Adinolfi S; Bagni C; Musco G; Gibson T; Mazzarella L; et al. Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains | 22 | 29 |
| 2588 | 28 | 41 | 2344 2002 RNA-A PUBLICATION OF THE RNA SOCIETY 8(12):1482-1488 Primerano B; Tassone F; Hagerman RJ; Hagerman P; Amaldi F; et al. Reduced FMR1 mRNA translation efficiency in Fragile X patients with premutations | 11 | 14 |
| 2589 | 18 | 33 | 2475 2003 RNA-A PUBLICATION OF THE RNA SOCIETY 9(10):1198-1207 Ramos A; Hollingworth D; Pastore A G-quartet-dependent recognition between the FMRP RGG box and RNA | 7 | 12 |
| 2590 | 3 | 31 | 613 1988 SCHIZOPHRENIA RESEARCH 1(4):277-281 DELISI LE; REISS AL; WHITE BJ; GERSHON ES CYTOGENETIC STUDIES OF MALES WITH SCHIZOPHRENIA - SCREENING FOR THE FRAGILE X-CHROMOSOME AND OTHER CHROMOSOMAL-ABNORMALITIES | 1 | 36 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2591 | 0 | 22 | 2345 2002 SCHIZOPHRENIA RESEARCH 58(1):37-41 Akahane A; Kunugi H; Tanaka H; Nanko S Association analysis of polymorphic CGG repeat in 5 ' UTR of the reelin and VLDLR genes with schizophrenia | 0 | 4 |
| 2592 | 5 | 52 | 164 1983 SCHWEIZERISCHE MEDIZINISCHE WOCHENSCHRIFT 113(7):238-244 ZOLLINGER A; SCHMID W; VILAN J; SORG B; KNOBLAUCH M X-LINKED MENTAL-RETARDATION WITH FRAGILE X-CHROMOSOME AND MACROORCHIDISM | 3 | 3 |
| 2593 | 12 | 37 | 497 1987 SCIENCE 237(4813):420-423 WARREN ST; ZHANG FP; LICAMELI GR; PETERS JF THE FRAGILE-X SITE IN SOMATIC-CELL HYBRIDS - AN APPROACH FOR MOLECULAR-CLONING OF FRAGILE SITES | 30 | 71 |
| 2594 | 0 | 3 | 669 1989 SCIENCE 243(4888):171-172 BARNES DM FRAGILE-X SYNDROME AND ITS PUZZLING GENETICS | 3 | 9 |
| 2595 | 4 | 22 | 670 1989 SCIENCE 246(4935):1298-1300 SUTHERS GK; CALLEN DF; HYLAND VJ; KOZMAN HM; BAKER E; et al. A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) | 31 | 66 |
| 2596 | 9 | 33 | 903 1991 SCIENCE 251(4998):1236-1239 HEITZ D; ROUSSEAU F; DEVYS D; SACCONE S; ABDERRAHIM H; et al. ISOLATION OF SEQUENCES THAT SPAN THE FRAGILE-X AND IDENTIFICATION OF A FRAGILE-X RELATED CPG ISLAND | 87 | 139 |
| 2597 | 0 | 0 | 904 1991 SCIENCE 252(5009):1070-1070 HOFFMAN M UNRAVELING THE GENETICS OF FRAGILE X-SYNDROME | 2 | 4 |
| 2598 | 18 | 37 | 905 1991 SCIENCE 252(5009):1097-1102 OBERLE I; ROUSSEAU F; HEITZ D; KRETZ C; DEVYS D; et al. INSTABILITY OF A 550 BASE PAIR DNA SEGMENT AND ABNORMAL METHYLATION IN FRAGILE X-SYNDROME | 440 | 846 |
| 2599 | 3 | 9 | 906 1991 SCIENCE 252(5009):1179-1181 YU S; PRITCHARD M; KREMER E; LYNCH M; NANCARROW J; et al. FRAGILE-X GENOTYPE CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 295 | 542 |
| 2600 | 5 | 13 | 907 1991 SCIENCE 252(5013):1711-1714 KREMER EJ; PRITCHARD M; LYNCH M; YU S; HOLMAN K; et al. MAPPING OF DNA INSTABILITY AT THE FRAGILE-X TO A TRINUCLEOTIDE REPEAT SEQUENCE P(CCG)N | 218 | 584 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2601 | 3 | 4 | 908 1991 SCIENCE 253(5027):1467-1467 HECHT F FRAGILE-X GENE | 0 | 0 |
| 2602 | 0 | 0 | 2212 2001 SCIENCE 294(5548):1809-1809 Sohn E Genetics - Fragile X's missing partners identified | 0 | 1 |
| 2603 | 10 | 13 | 2213 2001 SCIENCE 294(5551):2487-2488 Moine H; Mandel JL Biomedicine - Do G quartets orchestrate fragile X pathology? | 4 | 9 |
| 2604 | 2 | 10 | 1165 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 |
| 2605 | 0 | 0 | 2346 2002 SCIENTIST 16(20):8-8 Johnston N Fragile X, an RNAi connection? | 0 | 0 |
| 2606 | 28 | 77 | 1575 1996 SCREENING 4(4):175-192 Meadows KL; Sherman SL Fragile X syndrome: Examination of issues pertaining to population-based screening | 2 | 2 |
| 2607 | 13 | 27 | 2214 2001 SEIZURE-EUROPEAN JOURNAL OF EPILEPSY 10(1):60-63 Sabaratnam M; Vroegop PG; Gangadharan SK Epilepsy and EEG findings in 18 males with fragile X syndrome | 4 | 6 |
| 2608 | 4 | 11 | 312 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 |
| 2609 | 42 | 70 | 1439 1995 SEMINARS IN CELL BIOLOGY 6(1):5-11 NELSON DL THE FRAGILE-X SYNDROMES | 4 | 16 |
| 2610 | 70 | 102 | 2215 2001 SEMINARS IN REPRODUCTIVE MEDICINE 19(2):159-165 Kenneson A; Warren ST The female and the fragile X reviewed | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2611 | 6 | 24 | 237 1984 SOMATIC CELL AND MOLECULAR GENETICS 10(4):409-413 WARREN ST; DAVIDSON RL EXPRESSION OF FRAGILE X-CHROMOSOME IN HUMAN RODENT SOMATIC-CELL HYBRIDS | 14 | 19 |
| 2612 | 4 | 15 | 313 1985 SOMATIC CELL AND MOLECULAR GENETICS 11(4):353-357 WANG JCC; ERBE RW THYMIDYLATE METABOLISM IN FRAGILE-X SYNDROME CELLS | 3 | 5 |
| 2613 | 11 | 27 | 1166 1993 SOMATIC CELL AND MOLECULAR GENETICS 19(4):393-404 LUO SY; ROBINSON JC; REISS AL; MIGEON BR DNA METHYLATION OF THE FRAGILE-X LOCUS IN SOMATIC AND GERM-CELLS DURING FETAL DEVELOPMENT - RELEVANCE TO THE FRAGILE-X SYNDROME AND X-INACTIVATION | 6 | 19 |
| 2614 | 19 | 35 | 1576 1996 SOMATIC CELL AND MOLECULAR GENETICS 22(6):435-441 Eberhart DE; Warren ST Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus | 7 | 15 |
| 2615 | 4 | 10 | 1709 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 |
| 2616 | 12 | 26 | 413 1986 SOUTHERN MEDICAL JOURNAL 79(4):405-409 YOUNG RS; JARAMILLO C; MCCOMBS JL; MOORE CM; JORGENSON RJ FRAGILE-X MENTAL-RETARDATION SYNDROME TRANSMITTED THROUGH INTELLECTUALLY NORMAL MALES - IMPLICATIONS FOR GENETIC-COUNSELING | 3 | 6 |
| 2617 | 2 | 13 | 1797 1998 STEROIDS 63(1):2-4 Joseph DR The rat androgen-binding protein (ABP/SHBG) gene contains triplet repeats similar to unstable triplets: Evidence that the ABP/SHBG and the fragile X-related 2 genes overlap | 0 | 9 |
| 2618 | 0 | 0 | 165 1983 TERATOLOGY 28(1):A30-A30 ISHIKIRIYAMA S; NIIKAWA N 2 JAPANESE PATIENTS WITH FRAGILE X SYNDROME | 0 | 2 |
| 2619 | 0 | 0 | 498 1987 TERATOLOGY 36(3):453-453 SUZUKI Y; CHYO H; MATSUI A; SHIMOMURA C; FUNAHASI M CLINICAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 1 | 2 |
| 2620 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2621 | 9 | 27 | 1167 1993 TRENDS IN BIOCHEMICAL SCIENCES 18(9):331-333 GIBSON TJ; RICE PM; THOMPSON JD; HERINGA J KH DOMAINS WITHIN THE FMR1 SEQUENCE SUGGEST THAT FRAGILE-X SYNDROME STEMS FROM A DEFECT IN RNA-METABOLISM | 22 | 60 |
| 2622 | 37 | 55 | 2476 2003 TRENDS IN BIOCHEMICAL SCIENCES 28(3):152-158 Jin P; Warren ST New insights into fragile X syndrome: from molecules to neurobehaviors | 18 | 34 |
| 2623 | 5 | 17 | 314 1985 TRENDS IN GENETICS 1(4):108-112 SUTHERLAND GR THE ENIGMA OF THE FRAGILE-X CHROMOSOME | 26 | 43 |
| 2624 | 26 | 44 | 1027 1992 TRENDS IN GENETICS 8(7):249-255 RICHARDS RI; SUTHERLAND GR FRAGILE X-SYNDROME - THE MOLECULAR PICTURE COMES INTO FOCUS | 13 | 39 |
| 2625 | 36 | 60 | 2477 2003 TRENDS IN GENETICS 19(3):148-154 Kooy RF Of mice and the fragile X syndrome | 10 | 13 |
| 2626 | 59 | 77 | 2647 2005 TRENDS IN GENETICS 21(1):37-45 Zhang YQ; Broadie K Fathoming fragile X in fruit flies | 1 | 1 |
| 2627 | 13 | 15 | 2347 2002 TRENDS IN MOLECULAR MEDICINE 8(3):102-103 Oostra BA Functions of the fragile X protein | 6 | 8 |
| 2628 | 24 | 48 | 414 1986 TRENDS IN NEUROSCIENCES 9(2):58-62 PEMBREY ME; WINTER RM; DAVIES KE FRAGILE X MENTAL-RETARDATION - CURRENT CONTROVERSIES | 7 | 9 |
| 2629 | 33 | 95 | 2619 2004 TRENDS IN NEUROSCIENCES 27(7):370-377 Bear MF; Huber KM; Warren ST The mGIuR theory of fragile X mental retardation | 8 | 10 |
| 2630 | 18 | 33 | 1577 1996 VARIATION IN THE HUMAN GENOME 197:119-126 Sutherland GR; Richards RI Unusual inheritance patterns due to dynamic mutation in fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2631 | 5 | 20 | 1578 1996 VARIATION IN THE HUMAN GENOME 197:126-136 Weiss KM; Sutherland GR; Harper PS; Bodmer W; Bowcock AM; et al. Unusual inheritance patterns due to dynamic mutation in fragile X syndrome - Discussion | 0 | 0 |
| 2632 | 1 | 10 | 2092 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 |
| 2633 | 5 | 37 | 87 1982 WESTERN JOURNAL OF MEDICINE 137(4):278-281 MOORE BC; GLOVER TW; KAISERMCCAW B; HECHT F FRAGILE X-LINKED MENTAL-RETARDATION AND MACRO-ORCHIDISM | 1 | 3 |
| 2634 | 76 | 123 | 1710 1997 WESTERN JOURNAL OF MEDICINE 166(2):129-137 Hagerman RJ Fragile X syndrome - Molecular and clinical insights and treatment issues | 6 | 8 |
| 2635 | 0 | 21 | 88 1982 WIENER KLINISCHE WOCHENSCHRIFT 94(8):217-219 FONATSCH C; FLATZ SD FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 2636 | 7 | 34 | 739 1990 YALE JOURNAL OF BIOLOGY AND MEDICINE 63(4):293-299 BREGMAN JD; LECKMAN JF; ORT SI THYROID-FUNCTION IN FRAGILE-X SYNDROME MALES | 6 | 8 |
| 2637 | 12 | 40 | 2478 2003 YONSEI MEDICAL JOURNAL 44(4):583-592 Demirhan O; Tastemir D; Diler RS; Firat S; Avei A A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome | 1 | 1 |
| 2638 | 3 | 22 | 1168 1993 YOUNG CHILDREN 49(1):73-77 MAZZOCCO MMM; OCONNOR R FRAGILE-X SYNDROME - A GUIDE FOR TEACHERS OF YOUNG-CHILDREN | 0 | 1 |
| 2639 | 2 | 3 | 671 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):85-90 BLANK R MAIN SYMPTOMS - DELAYED LANGUAGE-DEVELOPMENT AND BEHAVIOR PROBLEMS - 2 CASE-REPORTS ON THE FRAGILE-X SYNDROME | 1 | 1 |
| 2640 | 30 | 39 | 672 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):91-97 VONGONTARD A PSYCHOPATHOLOGY ASSOCIATED WITH THE FRAGILE-X SYNDROME | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2641 | 19 | 26 | 1028 1992 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 20(2):113-120 VONGONTARD A; HILLIG U; HEROLD D CLINICAL AND CYTOGENETIC PROBLEMS IN THE DIAGNOSIS OF THE FRAGILE-X SYNDROME | 1 | 1 |
| 2642 | 10 | 20 | 1934 1999 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 27(3):175-181 Sarimski K Play and communicative behaviour in young boys with fragile-X syndrome. | 0 | 1 |
| 2643 | 0 | 0 | 614 1988 ZEITSCHRIFT FUR KLINISCHE MEDIZIN-ZKM 43(6):451-454 STEINBICKER V; SEEMANOVA E; MISSBACH D THE SYNDROME OF THE FRAGILE X (MARTIN-BELL-SYNDROME MBS) | 0 | 1 |
| 2644 | 0 | 0 | 673 1989 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 89(8):101-105 BLYUMINA MG CLINICAL SIGNS OF OLIGOPHRENIA WITH FRAGILE X-CHROMOSOME IN PREPUBERTY AND POSTPUBERTY MALES | 1 | 2 |
| 2645 | 4 | 9 | 1029 1992 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 92(4):28-31 LASTOCHKINA NA; KUPRIYANOVA TA; PUCHINSKAYA LM; MARINCHEVA GS; GORKOVA SA THE CLINICOELECTROPHYSIOLOGICAL CHARACTERIZATION OF WOMEN, HETEROZYGOUS CARRIERS OF FRAGILE X-CHROMOSOME | 1 | 1 |
| 2646 | 8 | 22 | 1711 1997 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 97(8):33-37 Gorbachevskaya NL; Denisova LV Bioelectric brain activity in patients with syndrome of fragile X-chromosome and in their mothers | 0 | 1 |
| 2647 | 71 | 143 | 1798 1998 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 98(9):54-63 Vorsanova SG; Vekhova NV; Demidova IA; Yurov YB Syndrome of mental retardation, linked with fragile X-chromosome: problems of diagnostics and inheritance | 0 | 0 |