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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 501 | 14 | 19 | 2040 2001 JOURNAL OF MEDICAL GENETICS 38(7):453-456 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA | 13 | 19 |
| 502 | 14 | 47 | 2102 2002 AMERICAN JOURNAL OF NEURORADIOLOGY 23(10):1757-1766 Brunberg JA; Jacquemont S; Hagerman RJ; Berry-Kravis EM; Grigsby J; Leehey MA; Tassone F; Brown WT; Greco CM; Hagerman PJ Fragile X premutation carriers: Characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction | 11 | 19 |
| 503 | 18 | 36 | 2200 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(4):869-878 Jacquemont S; Hagerman RJ; Leehey M; Grigsby J; Zhang L; Brunberg JA; Greco C; Des Portes V; Jardini T; Levine R; Berry-Kravis E; Brown WT; Schaeffer S; Kissel J; Tassone F; Hagerman PJ Fragile X premutation tremor/ataxia syndrome: Molecular, clinical, and neuroimaging correlates | 10 | 19 |
| 504 | 5 | 13 | 66 1982 HUMAN GENETICS 62(3):285-286 SCHMIDT A; PASSARGE E; SEEMANOVA E; MACEK M PRENATAL DETECTION OF A FETUS HEMIZYGOUS FOR THE FRAGILE X-CHROMOSOME | 12 | 18 |
| 505 | 13 | 68 | 141 1983 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 4(2):122-130 HAGERMAN RJ; MCBOGG P; HAGERMAN PJ THE FRAGILE-X SYNDROME - HISTORY, DIAGNOSIS, AND TREATMENT | 14 | 18 |
| 506 | 8 | 31 | 143 1983 JOURNAL OF MEDICAL GENETICS 20(3):169-178 MCDERMOTT A; WALTERS R; HOWELL RT; GARDNER A FRAGILE X-CHROMOSOME - CLINICAL AND CYTOGENETIC STUDIES ON CASES FROM 7 FAMILIES | 13 | 18 |
| 507 | 7 | 13 | 338 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):429-443 LEDBETTER DH; AIRHART SD; NUSSBAUM RL SOMATIC-CELL HYBRID STUDIES OF FRAGILE-(X) EXPRESSION IN A CARRIER FEMALE AND TRANSMITTING MALE | 10 | 18 |
| 508 | 1 | 14 | 339 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):445-455 LEDBETTER DH; AIRHART SD; NUSSBAUM RL CAFFEINE ENHANCES FRAGILE-(X) EXPRESSION IN SOMATIC-CELL HYBRIDS | 5 | 18 |
| 509 | 12 | 22 | 492 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 |
| 510 | 13 | 26 | 1164 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):364-369 LACHIEWICZ AM; DAWSON DV BEHAVIOR PROBLEMS OF YOUNG GIRLS WITH FRAGILE-X-SYNDROME - FACTOR SCORES ON THE CONNERS PARENTS QUESTIONNAIRE | 11 | 18 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 511 | 15 | 21 | 1181 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):466-470 HOFSTEE Y; ARINAMI T; HAMAGUCHI H COMPARISON BETWEEN THE CYTOGENETIC TEST FOR FRAGILE-X AND THE MOLECULAR ANALYSIS OF THE FMR-1 GENE IN JAPANESE MENTALLY-RETARDED INDIVIDUALS | 12 | 18 |
| 512 | 19 | 64 | 1211 1994 DEVELOPMENTAL BRAIN DYSFUNCTION 7(2-3):155-164 HAGERMAN RJ; FULTON MJ; LEAMAN A; RIDDLE J; HAGERMAN K; SOBESKY W A SURVEY OF FLUOXETINE THERAPY IN FRAGILE-X SYNDROME | 16 | 18 |
| 513 | 5 | 21 | 1422 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):266-267 Wohrle D; Schwemmle S; Steinbach P DNA methylation and triplet repeat stability: New proposals addressing actual questions on the CGG repeat of fragile X syndrome | 9 | 18 |
| 514 | 21 | 35 | 1425 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):287-292 Brown WT; Houck GE; Ding XH; Zhong N; Nolin S; Glicksman A; Dobkin C; Jenkins EC Reverse mutations in the fragile X syndrome | 9 | 18 |
| 515 | 13 | 41 | 1734 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):313-317 Hagerman RJ; Hills J; Scharfenaker S; Lewis H Fragile X syndrome and selective mutism | 11 | 18 |
| 516 | 18 | 37 | 1744 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):184-190 Patsalis PC; Sismani C; Hettinger JA; Boumba I; Georgiou I; Stylianidou G; Anastasiadou V; Koukoulli R; Pagoulatos G; Syrrou M Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: Incidence, genetic variation, and stability | 7 | 18 |
| 517 | 22 | 54 | 1782 1999 EPILEPSIA 40(8):1092-1099 Musumeci SA; Hagerman RJ; Ferri R; Bosco P; Dalla Bernardina B; Tassinari CA; De Sarro GB; Elia M Epilepsy and EEG findings in males with fragile X syndrome | 9 | 18 |
| 518 | 30 | 45 | 1951 2000 MOLECULAR MEDICINE TODAY 6(5):193-198 Kooy RF; Willemsen R; Oostra BA Fragile X syndrome at the turn of the century | 12 | 18 |
| 519 | 26 | 57 | 2145 2002 HUMAN MOLECULAR GENETICS 11(24):3007-3017 Mazroui R; Huot ME; Tremblay S; Filion C; Labelle Y; Khandjian EW Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression | 10 | 18 |
| 520 | 1 | 13 | 114 1983 ANNALES DE GENETIQUE 26(4):251-253 FRYNS JP; KLECZKOWSKA A; KUBIEN E; PETIT P; HASPESLAGH M; LINDEMANS I; VANDENBERGHE H XY XXY MOSAICISM AND FRAGILE X-SYNDROME | 12 | 17 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 521 | 1 | 4 | 128 1983 CLINICAL GENETICS 24(5):320-323 DEARCE MA TABLES FOR THE CYTOGENETIC STUDY OF FRAGILE X-CHROMOSOMES FOR DIAGNOSTIC PURPOSES | 11 | 17 |
| 522 | 1 | 12 | 171 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):123-131 HAGERMAN RJ; SYNHORST DP MITRAL-VALVE PROLAPSE AND AORTIC DILATATION IN THE FRAGILE-X SYNDROME | 9 | 17 |
| 523 | 9 | 16 | 387 1986 HUMAN GENETICS 74(1):93-97 WINTER RM; PEMBREY ME ANALYSIS OF LINKAGE RELATIONSHIPS BETWEEN GENETIC-MARKERS AROUND THE FRAGILE X LOCUS WITH SPECIAL REFERENCE TO THE DAUGHTERS OF NORMAL TRANSMITTING MALES | 13 | 17 |
| 524 | 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 |
| 525 | 1 | 13 | 571 1988 CLINICAL GENETICS 33(5):349-355 MERYASH DL; ABUELO D COUNSELING NEEDS AND ATTITUDES TOWARD PRENATAL-DIAGNOSIS AND ABORTION IN FRAGILE-X FAMILIES | 5 | 17 |
| 526 | 4 | 30 | 587 1988 HUMAN GENETICS 79(4):292-296 LI SY; TSAI CC; CHOU MY; LIN JK A CYTOGENETIC STUDY OF MENTALLY-RETARDED SCHOOL-CHILDREN IN TAIWAN WITH SPECIAL REFERENCE TO THE FRAGILE X-CHROMOSOME | 6 | 17 |
| 527 | 15 | 17 | 937 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):268-278 MALMGREN H; STEENBONDESON ML; GUSTAVSON KH; SEEMANOVA E; HOLMGREN G; OBERLE I; MANDEL JL; PETTERSSON U; DAHL N METHYLATION AND MUTATION PATTERNS IN THE FRAGILE-X SYNDROME | 13 | 17 |
| 528 | 8 | 22 | 1154 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):294-297 ALBRIGHT SG; LACHIEWICZ AM; TARLETON JC; RAO KW; SCHWARTZ CE; RICHIE R; TENNISON MB; AYLSWORTH AS FRAGILE-X PHENOTYPE IN A PATIENT WITH A LARGE DE-NOVO DELETION IN XQ27-Q28 | 10 | 17 |
| 529 | 10 | 23 | 1209 1994 CLINICAL GENETICS 45(4):175-180 SCHRANDERSTUMPEL C; GERVER WJ; MEYER H; ENGELEN J; MULDER H; FRYNS JP PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X SYNDROME | 4 | 17 |
| 530 | 14 | 31 | 1254 1994 PEDIATRICS 93(6):992-995 LACHIEWICZ AM; DAWSON DV DO YOUNG BOYS WITH FRAGILE-X-SYNDROME HAVE MACROORCHIDISM | 13 | 17 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 531 | 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 |
| 532 | 10 | 12 | 1409 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):181-183 Spence WC; Black SH; Fallon L; Maddalena A; Cummings E; MenapaceDrew G; Bick DP; Levinson G; Schulman JD; HowardPeebles PN Molecular fragile X screening in normal populations | 13 | 17 |
| 533 | 20 | 37 | 1949 2000 MOLECULAR BRAIN RESEARCH 80(1):17-25 Todd PK; Mack KJ Sensory stimulation increases cortical expression of the fragile X mental retardation protein in vivo | 15 | 17 |
| 534 | 10 | 17 | 1961 2000 PRENATAL DIAGNOSIS 20(8):611-614 Pesso R; Berkenstadt H; Cuckle H; Gak E; Peleg L; Frydman M; Barkai G Screening for fragile X syndrome in women of reproductive age | 13 | 17 |
| 535 | 35 | 51 | 2116 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(3):278-283 Hagerman RJ; Hagerman PJ The fragile X premutation: into the phenotypic fold | 6 | 17 |
| 536 | 3 | 25 | 174 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):195-207 SIMPSON NE; NEWMAN BJ; PARTINGTON MW FRAGILE-X SYNDROME .3. DERMATOGLYPHIC STUDIES IN MALES | 10 | 16 |
| 537 | 3 | 44 | 220 1984 JOURNAL OF SPEECH AND HEARING DISORDERS 49(3):328-332 PAUL R; COHEN DJ; BREG WR; WATSON M; HERMAN S FRAGILE-X SYNDROME - ITS RELATIONS TO SPEECH AND LANGUAGE DISORDERS | 12 | 16 |
| 538 | 1 | 3 | 347 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):567-572 JACOBS PA; MAYER M; ABRUZZO MA STUDIES OF THE FRAGILE (X) SYNDROME IN POPULATIONS OF MENTALLY-RETARDED INDIVIDUALS IN HAWAII | 13 | 16 |
| 539 | 11 | 29 | 353 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):701-713 FRIEDMAN JM; HOWARDPEEBLES PN INHERITANCE OF FRAGILE-X SYNDROME - AN HYPOTHESIS | 10 | 16 |
| 540 | 6 | 13 | 395 1986 JOURNAL OF MEDICAL GENETICS 23(5):407-410 TUCKERMAN E; WEBB T; THAKE A REPLICATION STATUS OF FRAGILE X(Q27.3) IN 13 FEMALE HETEROZYGOTES | 12 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 541 | 17 | 36 | 423 1987 ANNALS OF HUMAN GENETICS 51:107-124 GIANNELLI F; MORRIS AH; GARRETT C; DAKER M; THURSTON C; SMITH CAB GENETIC-HETEROGENEITY OF X-LINKED MENTAL-RETARDATION WITH FRAGILE-X - ASSOCIATION OF TIGHT LINKAGE TO FACTOR-IX AND INCOMPLETE PENETRANCE IN MALES | 7 | 16 |
| 542 | 6 | 34 | 429 1987 BIOLOGICAL PSYCHIATRY 22(3):303-312 STCLAIR DM; BLACKWOOD DHR; OLIVER CJ; DICKENS P P3 ABNORMALITY IN FRAGILE-X SYNDROME | 5 | 16 |
| 543 | 16 | 30 | 455 1987 HUMAN GENETICS 76(2):165-172 BUCHANAN JA; BUCKTON KE; GOSDEN CM; NEWTON MS; CLAYTON JF; CHRISTIE S; HASTIE N 10 FAMILIES WITH FRAGILE-X SYNDROME - LINKAGE RELATIONSHIPS WITH 4 DNA PROBES FROM DISTAL-XQ | 9 | 16 |
| 544 | 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 |
| 545 | 16 | 24 | 590 1988 HUMAN GENETICS 80(4):375-378 VOELCKEL MA; MATTEI MG; NGUYEN C; PHILIP N; BIRG F; MATTEI JF DISSOCIATION BETWEEN MENTAL-RETARDATION AND FRAGILE SITE EXPRESSION IN A FAMILY WITH FRAGILE X-LINKED MENTAL-RETARDATION | 8 | 16 |
| 546 | 10 | 14 | 620 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):302-303 COHEN IL; BROWN WT; JENKINS EC; KRAWCZUN MS; FRENCH JH; RAGUTHU S; WOLFSCHEIN EG; SUDHALTER V; FISCH G; WISNIEWSKI K FRAGILE-X SYNDROME IN FEMALES WITH AUTISM | 13 | 16 |
| 547 | 9 | 32 | 685 1990 AMERICAN JOURNAL ON MENTAL RETARDATION 94(4):442-447 CANTU ES; STONE JW; WING AA; LANGEE HR; WILLIAMS CA CYTOGENETIC SURVEY FOR AUTISTIC FRAGILE-X CARRIERS IN A MENTAL-RETARDATION CENTER | 5 | 16 |
| 548 | 24 | 44 | 694 1990 CLINICAL GENETICS 37(1):2-11 SUTHERLAND GR; MULLEY JC DIAGNOSTIC MOLECULAR-GENETICS OF THE FRAGILE-X | 14 | 16 |
| 549 | 13 | 22 | 936 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):244-254 SNOW K; DOUD L; HAGERMAN R; HULL C; HIRST MC; DAVIES KE; THIBODEAU SL ANALYSIS OF MUTATIONS AT THE FRAGILE-X LOCUS USING THE DNA PROBE OX1.9 | 14 | 16 |
| 550 | 7 | 15 | 952 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(6):1057-1062 WEBB T DELAYED REPLICATION OF XQ27 IN INDIVIDUALS WITH THE FRAGILE X-SYNDROME | 2 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 551 | 11 | 13 | 1187 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):497-500 SMITS A; SMEETS D; HAMEL B; DREESEN J; DEHAAN A; VANOOST B PREDICTION OF MENTAL STATUS IN CARRIERS OF THE FRAGILE-X MUTATION USING CGG REPEAT LENGTH | 13 | 16 |
| 552 | 21 | 34 | 1216 1994 HUMAN GENETICS 94(4):395-400 MILA M; KRUYER H; GLOVER G; SANCHEZ A; CARBONELL P; CASTELLVIBEL S; VOLPINI V; ROSELL J; GABARRON J; LOPEZ I; VILLA M; BALLESTA F; ESTIVILL X MOLECULAR ANALYSIS OF THE (CGG)(N) EXPANSION IN THE FMR-1 GENE IN 59 SPANISH FRAGILE-X SYNDROME FAMILIES | 12 | 16 |
| 553 | 40 | 70 | 1392 1995 SEMINARS IN CELL BIOLOGY 6(1):5-11 NELSON DL THE FRAGILE-X SYNDROMES | 3 | 16 |
| 554 | 17 | 21 | 1420 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):256-260 Sherman SL; Meadows KL; Ashley AE Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females | 12 | 16 |
| 555 | 15 | 26 | 1482 1996 HUMAN GENETICS 97(6):808-812 Haddad LA; MingroniNetto RC; ViannaMorgante AM; Pena SDJ A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males | 7 | 16 |
| 556 | 3 | 4 | 1499 1996 LANCET 348(9032):967-968 Willemsen R; Oosterwijk JC; Los FJ; Galjaard H; Oostra BA Prenatal diagnosis of fragile X syndrome | 11 | 16 |
| 557 | 10 | 33 | 1678 1998 JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS 15(4):745-756 Chen X; Mariappan SVS; Moyzis RK; Bradbury EM; Gupta G Hairpin induced slippage and hyper-methylation of the fragile X DNA triplets | 4 | 16 |
| 558 | 7 | 40 | 1679 1998 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 39(5):699-710 van Lieshout CFM; De Meyer RE; Curfs LMG; Fryns JP Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome | 4 | 16 |
| 559 | 6 | 39 | 1688 1998 JOURNAL OF MOLECULAR BIOLOGY 283(1):111-120 Mariappan SVS; Silks LA; Bradbury EM; Gupta G Fragile X DNA triplet repeats, (GCC)(n), form hairpins with single hydrogen-bonded cytosine center dot cytosine mispairs at the CpG sites: Isotope-edited nuclear magnetic resonance spectroscopy on (GCC)(n) with selective (15)N4-labeled cytosine bases | 4 | 16 |
| 560 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 561 | 14 | 23 | 1783 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(2):212-216 Ryynanen M; Heinonen S; Makkonen M; Kajanoja E; Mannermaa A; Pertti K Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies | 12 | 16 |
| 562 | 26 | 52 | 1826 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):480-493 Crawford DC; Schwartz CE; Meadows KL; Newman JL; Taft LF; Gunter C; Brown WT; Carpenter NJ; Howard-Peebles PN; Monaghan KG; Nolin SL; Reiss AL; Feldman GL; Rohlfs EM; Warren ST; Sherman SL Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population | 7 | 16 |
| 563 | 2 | 4 | 1828 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):253-254 Murray A; Ennis S; Morton N No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers | 9 | 16 |
| 564 | 10 | 41 | 1904 2000 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 30(1):49-59 Bailey DB; Hatton DD; Mesibov G; Ament N; Skinner M Early development, temperament, and functional impairment in autism and fragile X syndrome | 14 | 16 |
| 565 | 12 | 31 | 2054 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 |
| 566 | 35 | 55 | 2307 2003 TRENDS IN BIOCHEMICAL SCIENCES 28(3):152-158 Jin P; Warren ST New insights into fragile X syndrome: from molecules to neurobehaviors | 8 | 16 |
| 567 | 5 | 24 | 290 1985 JAPANESE JOURNAL OF CANCER RESEARCH 76(10):977-983 HORI T; AYUSAWA D; GLOVER TW; SENO T EXPRESSION OF FRAGILE SITE ON THE HUMAN-X CHROMOSOME IN SOMATIC-CELL HYBRIDS BETWEEN HUMAN FRAGILE-X CELLS AND THYMIDYLATE SYNTHASE-NEGATIVE MOUSE MUTANT-CELLS | 3 | 15 |
| 568 | 9 | 27 | 328 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):273-289 FROSTERISKENIUS U; BODEKER K; OEPEN T; MATTHES R; PIPER U; SCHWINGER E FOLIC-ACID TREATMENT IN MALES AND FEMALES WITH FRAGILE-(X)- SYNDROME | 10 | 15 |
| 569 | 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 |
| 570 | 9 | 27 | 446 1987 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 29(6):711-719 THAKE A; TODD J; WEBB T; BUNDEY S CHILDREN WITH THE FRAGILE X-CHROMOSOME AT SCHOOLS FOR THE MILDLY MENTALLY-RETARDED | 11 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 571 | 7 | 33 | 454 1987 HUMAN GENETICS 76(2):141-147 JOHANNISSON R; REHDER H; WENDT V; SCHWINGER E SPERMATOGENESIS IN 2 PATIENTS WITH THE FRAGILE-X SYNDROME .1. HISTOLOGY - LIGHT AND ELECTRON-MICROSCOPY | 8 | 15 |
| 572 | 11 | 25 | 480 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(4):589-592 GOLDFINE PE; MCPHERSON PM; HARDESTY VA; HEATH GA; BEAUREGARD LJ; BAKER AA FRAGILE-X CHROMOSOME ASSOCIATED WITH PRIMARY LEARNING-DISABILITY | 12 | 15 |
| 573 | 1 | 3 | 499 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):1-17 NERI G; OPITZ JM; MIKKELSEN M; JACOBS PA; DAVIES K; TURNER G CONFERENCE REPORT - 3RD INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 6 | 15 |
| 574 | 7 | 16 | 545 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):641-654 SCHWARTZ CE; PHELAN MC; PULLIAM LH; WILKES G; VANNER LV; ALBIEZ KL; POTTS WA; ROGERS RC; SCHROER RJ; SAUL RA; PROUTY LA; DEAN JH; TAYLOR HA; STEVENSON RE FRAGILE-X SYNDROME - INCIDENCE, CLINICAL AND CYTOGENETIC FINDINGS IN THE BLACK AND WHITE-POPULATIONS OF SOUTH-CAROLINA | 12 | 15 |
| 575 | 5 | 12 | 555 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):753-765 SHERMAN SL; ROGATKO A; TURNER G RECURRENCE RISKS FOR RELATIVES IN FAMILIES WITH AN ISOLATED CASE OF THE FRAGILE X SYNDROME | 11 | 15 |
| 576 | 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 |
| 577 | 9 | 21 | 705 1990 HUMAN GENETICS 85(6):590-594 YU WD; WENGER SL; STEELE MW X-CHROMOSOME IMPRINTING IN FRAGILE-X SYNDROME | 6 | 15 |
| 578 | 11 | 25 | 804 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):391-395 LAIRD CD POSSIBLE ERASURE OF THE IMPRINT ON A FRAGILE-X CHROMOSOME WHEN TRANSMITTED BY A MALE | 8 | 15 |
| 579 | 7 | 15 | 822 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):503-504 CRONISTER A; HAGERMAN RJ; WITTENBERGER M; AMIRI K MENTAL IMPAIRMENT IN CYTOGENETICALLY POSITIVE FRAGILE-X FEMALES | 14 | 15 |
| 580 | 6 | 28 | 865 1991 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 21(4):503-516 HODAPP RM; DYKENS EM; ORT SI; ZELINSKY DG; LECKMAN JF CHANGING PATTERNS OF INTELLECTUAL STRENGTHS AND WEAKNESSES IN MALES WITH FRAGILE-X SYNDROME | 5 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 581 | 18 | 33 | 1190 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):517-521 CHIURAZZI P; KOZAK L; NERI G UNSTABLE TRIPLETS AND THEIR MUTATIONAL MECHANISM - SIZE-REDUCTION OF THE CGG REPEAT VS GERMLINE MOSAICISM IN THE FRAGILE-X-SYNDROME | 7 | 15 |
| 582 | 7 | 41 | 1252 1994 NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY 24(6):413-426 FERRI R; MUSUMECI SA; ELIA M; DELGRACCO S; SCUDERI C; BERGONZI P BIT-MAPPED SOMATOSENSORY-EVOKED POTENTIALS IN THE FRAGILE-X SYNDROME | 7 | 15 |
| 583 | 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 |
| 584 | 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 |
| 585 | 13 | 20 | 1417 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):234-238 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; Pagoulatos G Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus | 5 | 15 |
| 586 | 18 | 21 | 1429 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):309-312 Maddalena A; Yadvish KN; Spence WC; HowardPeebles PN A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in blood | 12 | 15 |
| 587 | 16 | 21 | 1438 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):365-369 Cohen IL; Nolin SL; Sudhalter V; Ding XH; Dobkin CS; Brown WT Mosaicism for the FMR1 gene influences adaptive skills development in fragile X-affected males | 14 | 15 |
| 588 | 10 | 13 | 1491 1996 JOURNAL OF MEDICAL GENETICS 33(4):338-340 Mila M; CastellviBel S; Sanchez A; Lazaro C; Villa M; Estivill X Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene | 9 | 15 |
| 589 | 13 | 42 | 1670 1998 JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES 11(3):175-191 Turk J Fragile X syndrome and attentional deficits | 11 | 15 |
| 590 | 17 | 41 | 1683 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:490-499 Turk J; Cornish K Face recognition and emotion perception in boys with fragile-X syndrome | 9 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 591 | 22 | 52 | 1703 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(3):680-688 Nolin SL; Houck GE; Gargano AD; Blumstein H; Dobkin CS; Brown WT FMR1 CCG-repeat instability by single sperm and lymphocytes of fragile-X premutation males | 7 | 15 |
| 592 | 6 | 8 | 1829 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):254-255 Vianna-Morgante AM; Costa SS Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X | 8 | 15 |
| 593 | 12 | 46 | 1859 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):307-315 Gould EL; Loesch DZ; Martin MJ; Hagerman RJ; Armstrong SM; Huggins RM Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study | 10 | 15 |
| 594 | 6 | 32 | 1911 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(5):315-321 Bailey DB; Skinner D; Hatton D; Roberts J Family experiences and factors associated with the diagnosis of fragile X syndrome | 12 | 15 |
| 595 | 13 | 47 | 1954 2000 NEUROPSYCHOLOGIA 38(9):1261-1270 Munir F; Cornish KM; Wilding J A neuropsychological profile of attention deficits in young males with fragile X syndrome | 13 | 15 |
| 596 | 16 | 33 | 2027 2001 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 31(2):165-174 Bailey DB; Hatton DD; Skinner M; Mesibov G Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome | 11 | 15 |
| 597 | 7 | 71 | 2029 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(21):18605-18613 Bacolla A; Pradhan S; Larson JE; Roberts RJ; Wells RD Recombinant human DNA (cytosine-5) methyltransferase - III. Allosteric control, reaction order, and influence of plasmid topology and triplet repeat length on methylation of the fragile X CGG center dot CCG sequence | 0 | 15 |
| 598 | 18 | 34 | 2033 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):409-417 Rogers SJ; Wehner EA; Hagerman R The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders | 9 | 15 |
| 599 | 15 | 43 | 2170 2002 MOLECULAR AND CELLULAR BIOLOGY 22(23):8332-8341 Otero YD; Severijnen LA; van Cappellen G; Schrier M; Oostra B; Willemsen R Transport of fragile X mental retardation protein via granules in neurites of PC12 cells | 6 | 15 |
| 600 | 2 | 5 | 63 1982 HUMAN GENETICS 61(3):254-255 EBERLE G; ZANKL M; ZANKL H THE EXPRESSION OF FRAGILE X-CHROMOSOMES IN MEMBERS OF THE SAME FAMILY AT DIFFERENT TIMES OF EXAMINATION | 12 | 14 |
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