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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 7: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 601 | 0 | 4 | 218 1984 JOURNAL OF MEDICAL GENETICS 21(5):373-373 FITCHETT M; SEABRIGHT M DELETED X-CHROMOSOMES IN PATIENTS WITH THE FRAGILE X-SYNDROME | 10 | 14 |
| 602 | 39 | 112 | 1309 1995 BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE 1271(2-3):293-303 FLANNERY AV; HIRST MC; KNIGHT SJL; RITCHIE RJ; DAVIES KE THE FRAGILE-X SYNDROME | 2 | 5 |
| 603 | 7 | 59 | 2259 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):140-146 Fleming K; Riser DK; Kumari D; Usdin K Instability of the fragile X syndrome repeat in mice: the effect of age, diet and mutations in genes that affect DNA replication, recombination and repair proficiency | 0 | 0 |
| 604 | 0 | 1 | 2031 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(5):337-337 Floet AW Children with fragile X syndrome: A parents' guide | 0 | 0 |
| 605 | 3 | 7 | 236 1985 ACTA PAEDIATRICA SCANDINAVICA 74(6):974-974 FLOOD A; SANNER G REFRACTIVE ERRORS IN THE FRAGILE-X SYNDROME | 3 | 3 |
| 606 | 13 | 27 | 2191 2002 PEDIATRICS 109(1) Flynn BJ; Myers SM; Cera PJ; Mowad JJ Testicular torsion in an adolescent with fragile X syndrome | 0 | 0 |
| 607 | 11 | 41 | 2363 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 | 0 |
| 608 | 5 | 47 | 2052 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 |
| 609 | 37 | 55 | 980 1992 HUMAN GENETICS 88(3):335-343 FOLLETTE PJ; LAIRD CD ESTIMATING THE STABILITY OF THE PROPOSED IMPRINTED STATE OF THE FRAGILE-X MUTATION WHEN TRANSMITTED BY FEMALES | 2 | 3 |
| 610 | 0 | 1 | 1518 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):191-192 Fombonne E The fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 611 | 12 | 16 | 1521 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):209-212 Fombonne E Epidemiological studies of fragile X syndrome | 0 | 0 |
| 612 | 0 | 3 | 19 1981 HUMAN GENETICS 59(2):186-186 FONATSCH C A SIMPLE METHOD TO DEMONSTRATE THE FRAGILE X-CHROMOSOME IN FIBROBLASTS | 21 | 38 |
| 613 | 1 | 1 | 118 1983 CLINICAL GENETICS 23(3):229-229 FONATSCH C FRAGILE X-CHROMOSOME IN FIBROBLASTS - LONGITUDINAL-STUDY ON TECHNICAL VARIATIONS | 3 | 3 |
| 614 | 0 | 21 | 85 1982 WIENER KLINISCHE WOCHENSCHRIFT 94(8):217-219 FONATSCH C; FLATZ SD FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 615 | 8 | 23 | 134 1983 HUMAN GENETICS 64(1):39-41 FONATSCH C; SCHWINGER E FREQUENCY OF FRAGILE-X CHROMOSOMES, FRA(X), IN LYMPHOCYTES IN RELATION TO BLOOD-STORAGE TIME AND CULTURE TECHNIQUES | 6 | 9 |
| 616 | 7 | 15 | 299 1985 JOURNAL OF NEUROGENETICS 2(3):231-237 FORSTERGIBSON CJ; MULLIGAN LM; PARTINGTON MW; SIMPSON NE; HOLDEN JJA; WHITE BN THE GENETIC-DISTANCE BETWEEN THE COAGULATION FACTOR-IX GENE AND THE LOCUS FOR THE FRAGILE-X SYNDROME - CLINICAL IMPLICATIONS | 13 | 23 |
| 617 | 58 | 71 | 1476 1996 EUROPEAN PSYCHIATRY 11(5):233-243 Franke P; Barbe B; Leboyer M; Maier W Fragile X syndrome .2. Cognitive and behavioral correlates of mutations of the FMR-1 gene | 4 | 5 |
| 618 | 12 | 18 | 1433 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):334-339 Franke P; Maier W; Hautzinger M; Weiffenbach O; Gansicke M; Iwers B; Poustka F; Schwab SG; Froster U Fragile-X carrier females: Evidence for a distinct psychopathological phenotype? | 19 | 28 |
| 619 | 11 | 41 | 2353 2004 MOLECULAR PSYCHIATRY 9(4):417-425 Frankland PW; Wang Y; Rosner B; Shimizu T; Balleine BW; Dykens EM; Ornitz EM; Silva AJ Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice | 0 | 0 |
| 620 | 0 | 0 | 1932 2000 JOURNAL OF MEDICAL GENETICS 37:S75-S75 Fratter C; Morsman A; Seller A Genetic analysis for Fragile X syndrome by fluorescent PCR | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 621 | 5 | 13 | 1760 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):197-201 Freedenberg DL; Gane LW; Richards CS; Lampe M; Hills J; O'Connor R; Manchester D; Taylor A; Tassone F; Hulseberg D; Hagerman RJ; Patil SR Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development | 1 | 1 |
| 622 | 17 | 33 | 1329 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):242-251 Freund LS; Peebles CD; Aylward E; Reiss AL Preliminary report on cognitive and adaptive behaviors of preschool-aged males with fragile X | 15 | 20 |
| 623 | 20 | 37 | 1143 1993 PEDIATRICS 91(2):321-329 FREUND LS; REISS AL; ABRAMS MT PSYCHIATRIC-DISORDERS ASSOCIATED WITH FRAGILE-X IN THE YOUNG FEMALE | 54 | 76 |
| 624 | 15 | 30 | 964 1992 ARCHIVES OF GENERAL PSYCHIATRY 49(1):54-60 FREUND LS; REISS AL; HAGERMAN R; VINOGRADOV S CHROMOSOME FRAGILITY AND PSYCHOPATHOLOGY IN OBLIGATE FEMALE CARRIERS OF THE FRAGILE X-CHROMOSOME | 25 | 44 |
| 625 | 15 | 39 | 1473 1996 EMBO JOURNAL 15(19):5408-5414 Fridell RA; Benson RE; Hua J; Bogerd HP; Cullen BR A nuclear role for the fragile X mental retardation protein | 32 | 65 |
| 626 | 0 | 0 | 195 1984 CLINICAL RESEARCH 32(5):A884-A884 FRIEDMAN JM; HOWARDPEEBLES PN A THEORETICAL-MODEL FOR UNAFFECTED CARRIER MALES IN FRAGILE-X FAMILIES | 0 | 0 |
| 627 | 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 |
| 628 | 4 | 13 | 1141 1993 NERVENHEILKUNDE 12(2):84-86 FROSTER UG CLINICAL AND MOLECULAR ASPECTS OF THE FRAGILE-X FORM OF MENTAL-RETARDATION (MARTIN-BELL SYNDROME) | 0 | 0 |
| 629 | 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 |
| 630 | 27 | 63 | 608 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 631 | 10 | 30 | 1256 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 | 26 | 142 |
| 632 | 7 | 41 | 1797 1999 JOURNAL OF BIOLOGICAL CHEMISTRY 274(18):12797-12802 Fry M; Loeb LA Human Werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)(n) | 9 | 96 |
| 633 | 21 | 64 | 194 1984 CLINICAL GENETICS 26(6):497-528 FRYNS JP THE FRAGILE X-SYNDROME - A STUDY OF 83 FAMILIES | 45 | 78 |
| 634 | 0 | 0 | 261 1985 CLINICAL GENETICS 27(3):307-307 FRYNS JP THE FRAGILE-X SYNDROME - A STUDY OF 83 INDEX-PATIENTS AND THEIR FAMILIES | 0 | 1 |
| 635 | 5 | 26 | 319 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):157-169 FRYNS JP THE FEMALE AND THE FRAGILE-X - A STUDY OF 144 OBLIGATE FEMALE CARRIERS | 76 | 101 |
| 636 | 1 | 4 | 1353 1995 GENETIC COUNSELING 6(4):293-296 FRYNS JP SCREENING FOR THE FRAGILE-X SYNDROME - THE NECESSITY OF INTERNATIONAL GUIDELINES FOR MOLECULAR-GENETICS PREDICTIVE TESTING IN GENERAL | 2 | 3 |
| 637 | 7 | 14 | 1479 1996 GENETIC COUNSELING 7(4):245-247 Fryns JP Ovarian function in fragile X carriers | 0 | 0 |
| 638 | 3 | 24 | 1855 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(5):345-360 Fryns JP; Borghgraef M; Brown TW; Chelly J; Fisch GS; Hamel B; Hanauer A; Lacombe D; Luo L; MacPherson JN; Mandel JL; Moraine C; Mulley J; Nelson D; Oostra B; Partington M; Ramakers GJA; Ropers HH; Rousseau F; Schwartz C; Steinbach P; Stoll C; Tranebjaerg L; Turner G; Van Bokhoven H; Vianna-Morgante A; Villard L; Warren ST 9th international workshop on fragile X syndrome and X-linked mental retardation | 0 | 2 |
| 639 | 0 | 4 | 1478 1996 GENETIC COUNSELING 7(3):227-230 Fryns JP; DHooghe M; Devriendt K Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 gene | 0 | 0 |
| 640 | 0 | 3 | 191 1984 CLINICAL GENETICS 25(2):131-134 FRYNS JP; JACOBS J; KLECZKOWSKA A; VANDENBERGHE H THE PSYCHOLOGICAL PROFILE OF THE FRAGILE X-SYNDROME | 56 | 75 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 641 | 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 |
| 642 | 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 |
| 643 | 2 | 11 | 193 1984 CLINICAL GENETICS 26(5):445-447 FRYNS JP; KLECZKOWSKA A; WOLFS I; VANDENBERGHE H KLINEFELTER SYNDROME AND 2 FRAGILE X-CHROMOSOMES | 15 | 21 |
| 644 | 2 | 3 | 64 1982 HUMAN GENETICS 61(3):262-263 FRYNS JP; VANDENBERGHE H TRANSMISSION OF FRAGILE (X)(Q27) FROM NORMAL MALE(S) | 25 | 35 |
| 645 | 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 |
| 646 | 3 | 8 | 531 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):401-406 FRYNS JP; VANDENBERGHE H INACTIVATION PATTERN OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 7 | 11 |
| 647 | 12 | 23 | 841 1991 CELL 67(6):1047-1058 FU YH; KUHL DPA; PIZZUTI A; PIERETTI M; SUTCLIFFE JS; RICHARDS S; VERKERK AJMH; HOLDEN JJA; FENWICK RG; WARREN ST; OOSTRA BA; NELSON DL; CASKEY CT VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX | 368 | 933 |
| 648 | 10 | 28 | 1584 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(2):89-93 FulchignoniLataud MC; Olchwang S; Serre JL The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients | 1 | 6 |
| 649 | 0 | 7 | 2071 2001 REVISTA DE NEUROLOGIA 33:S82-S87 Furgang R Language therapy in fragile X syndrome | 0 | 0 |
| 650 | 16 | 19 | 945 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):333-338 GABARRON J; LOPEZ I; GLOVER G; CARBONELL P FRAGILE-X SCREENING-PROGRAM IN A SPANISH REGION | 8 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 651 | 21 | 40 | 2364 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 | 0 | 0 |
| 652 | 12 | 41 | 2250 2003 BRAIN RESEARCH 971(1):83-89 Galvez R; Gopal AR; Greenough WT Somatosensory cortical barrel dendritic abnormalities in a mouse model of the fragile X mental retardation syndrome | 2 | 4 |
| 653 | 0 | 0 | 2134 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Gantois I; Reyniers E; Kooy F Differential gene expression in the fragile X mouse model | 0 | 0 |
| 654 | 0 | 0 | 1970 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):352-352 Gantois I; Reyniers E; Kooy RF Identification of genes differentially expressed in the fragile X syndrome. | 0 | 0 |
| 655 | 0 | 0 | 2217 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):557-557 Gantois I; Vandesompele J; Speleman F; D'Hooge R; Severijnen LA; Willemsen R; Tassone F; Kooy RF Expression profiling reveals involvement of the GABA(A) receptor subunit delta in the fragile X syndrome. | 0 | 0 |
| 656 | 9 | 20 | 2184 2002 NEURON 34(6):859-862 Gao FB Understanding fragile X syndrome: Insights from retarded flies | 3 | 6 |
| 657 | 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 |
| 658 | 0 | 4 | 76 1982 LANCET 1(8263):101-101 GARDNER AP; HOWELL RT; MCDERMOTT A FRAGILE-X CHROMOSOME - CONSISTENT DEMONSTRATION OF FRAGILE SITE IN FIBROBLAST-CULTURES | 10 | 14 |
| 659 | 8 | 12 | 185 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(4):853-855 GARDNER RJM FRAGILE-X MALES WITH NORMAL INTELLIGENCE - AND IF SO, WHY | 4 | 7 |
| 660 | 0 | 1 | 202 1984 HUMAN GENETICS 66(1):100-100 GARDNER RJM FRAGILE-X HOMOZYGOSITY DUE TO SOMATIC CROSSING-OVER | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 661 | 5 | 14 | 125 1983 CLINICAL GENETICS 23(4):311-317 GARDNER RJM; SMART RD; CORNELL JM; MERCKEL LM; BEIGHTON P THE FRAGILE X-CHROMOSOME IN A LARGE INDIAN KINDRED | 17 | 20 |
| 662 | 11 | 42 | 1802 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:466-474 Garner C; Callias M; Turk J Executive function and theory of mind performance of boys with fragile-X syndrome | 0 | 1 |
| 663 | 14 | 50 | 2320 2004 ARCHIVES OF GENERAL PSYCHIATRY 61(3):281-288 Garrett AS; Menon V; MacKenzie K; Reiss AL Here's looking at you, kid - Neural systems underlying face and gaze processing in fragile X syndrome | 0 | 0 |
| 664 | 0 | 0 | 563 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):93-94 GARRY MB; MACFARLANE SC; PULLON DHH FRAGILE-X POSITIVE TURNERS MOSAIC | 0 | 0 |
| 665 | 26 | 34 | 2265 2003 GENETIC TESTING 7(4):303-308 Gasteiger M; Grasbon-Frod E; Neitzel B; Kooy F; Holinski-Feder E FMR1 gene deletion/reversion: A pitfall of fragile X carrier testing | 0 | 0 |
| 666 | 10 | 23 | 1009 1992 NATURE GENETICS 1(5):341-344 GEDEON AK; BAKER E; ROBINSON H; PARTINGTON MW; GROSS B; MANCA A; KORN B; POUSTKA A; YU S; SUTHERLAND GR; MULLEY JC FRAGILE-X SYNDROME WITHOUT CCG AMPLIFICATION HAS AN FMR1 DELETION | 82 | 137 |
| 667 | 0 | 0 | 426 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):79-79 GEDEON AK; MULLEY JC; SUTHERLAND GR LINKAGE ANALYSIS AND CARRIER DETECTION OF THE FRAGILE-X | 0 | 0 |
| 668 | 12 | 42 | 1958 2000 NUCLEIC ACIDS RESEARCH 28(10):2141-2152 Genc B; Muller-Hartmann H; Zeschnigk M; Deissler H; Schmitz B; Majewski F; von Gontard A; Doerfler W Methylation mosaicism of 5 '-(CGG)(n)-3 ' repeats in fragile X, premutation and normal individuals | 3 | 6 |
| 669 | 1 | 15 | 34 1981 PEDIATRICS 68(4):594-595 GERALD PS X-LINKED MENTAL-RETARDATION AND THE FRAGILE-X SYNDROME | 5 | 11 |
| 670 | 0 | 0 | 82 1982 PEDIATRICS 69(5):669-669 GERALD PS X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME - REPLY | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 671 | 22 | 32 | 1561 1997 ANNALES DE GENETIQUE 40(3):139-144 Gerard B; LeHeuzey MF; Brunie G; Lewine P; Saiag MC; Cacheux V; DaSilva F; Dugas M; MourenSimeoni MC; Elion J; Grandchamp B Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children | 3 | 7 |
| 672 | 6 | 9 | 1523 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):224-226 Gerard CL; Guillotte E; Servel F; Barbeau M Assessment and remediation of communication disorders in children with fragile X syndrome | 0 | 0 |
| 673 | 0 | 0 | 1794 1999 HUMAN REPRODUCTION 14:354-355 Gersak K; Kregar-Velikonja N; Meden-Vrtovec H; Peterlin B Fragile X premutation screening in women with premature menopause | 1 | 1 |
| 674 | 20 | 29 | 2273 2003 HUMAN REPRODUCTION 18(8):1637-1640 Gersak K; Meden-Vrtovec H; Peterlin B Fragile X premutation in women with sporadic premature ovarian failure in Slovenia | 0 | 0 |
| 675 | 16 | 20 | 1890 2000 GENETIC TESTING 4(3):289-292 Geva E; Yaron Y; Shomrat R; Ben-Yehuda A; Zabari S; Peretz H; Naiman T; Yeger H; Orr-Urtreger A The risk of Fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known Fragile X families | 3 | 4 |
| 676 | 0 | 0 | 1903 2000 INFANT MENTAL HEALTH JOURNAL 21(4-5):330-330 Ghuman JK; Tierney E; Kau A; Reider E Social interaction problems in infants and preschool children with fragile-X syndrome, Smith-Lemli-Opitz syndrome and other developmental disorders | 0 | 0 |
| 677 | 11 | 24 | 1398 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 63(2):396-400 Giampietro PF; Haas BR; Lipper E; Gutman A; Zellers NJ; LaTrenta GS; Brooks SS; Matalon R; Kaul R; Ding XH; Brown WT Fragile X syndrome in two siblings with major congenital malformations | 0 | 1 |
| 678 | 0 | 0 | 1268 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):494-494 GIANGRECO CA; STEELE MW; ASTON CE; CUMMINS JH; WENGER SL CLINICAL-CRITERIA FOR FRAGILE-X SOUTHERN BLOT DNA DIAGNOSTIC TESTING | 0 | 0 |
| 679 | 12 | 14 | 1496 1996 JOURNAL OF PEDIATRICS 129(4):611-614 Giangreco CA; Steele MW; Aston CE; Cummins JH; Wenger SL A simplified six-item checklist for screening for fragile X syndrome in the pediatric population | 10 | 20 |
| 680 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 681 | 16 | 33 | 975 1992 EDUCATIONAL RESEARCH 34(3):221-228 GIBB C THE MOST COMMON-CAUSE OF LEARNING-DIFFICULTIES - A PROFILE OF FRAGILE-X SYNDROME AND ITS IMPLICATIONS FOR EDUCATION | 1 | 1 |
| 682 | 9 | 27 | 1148 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 | 21 | 59 |
| 683 | 4 | 6 | 2018 2001 GENETIC TESTING 5(2):139-140 Gilbert F Comment: How many are too many when discussing triplet repeats in the FMR1 gene and the fragile X syndrome? | 0 | 1 |
| 684 | 0 | 0 | 1000 1992 M S-MEDECINE SCIENCES 8(3):252-254 GILGENKRANTZ H FRAGILE-X - WHATS NEW | 0 | 0 |
| 685 | 7 | 8 | 209 1984 JOURNAL DE GENETIQUE HUMAINE 32(3):199-207 GILGENKRANTZ S; BOUE J; GREGOIRE MJ; TEJADA I MENTAL-RETARDATION AND (FRA-X) FRAGILE-X CHROMOSOME | 0 | 3 |
| 686 | 2 | 11 | 116 1983 BRITISH JOURNAL OF PSYCHIATRY 143(SEP):256-260 GILLBERG C IDENTICAL TRIPLETS WITH INFANTILE-AUTISM AND THE FRAGILE-X SYNDROME | 20 | 38 |
| 687 | 3 | 13 | 600 1988 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 29(4):447-451 GILLBERG C; OHLSON VA; WAHLSTROM J; STEFFENBURG S; BLIX K MONOZYGOTIC FEMALE TWINS WITH AUTISM AND THE FRAGILE-X SYNDROME (AFRAX) | 9 | 19 |
| 688 | 6 | 21 | 396 1986 JOURNAL OF MENTAL DEFICIENCY RESEARCH 30:27-39 GILLBERG C; PERSSON E; WAHLSTROM J THE AUTISM-FRAGILE-X SYNDROME (AFRAX) - A POPULATION-BASED STUDY OF 10 BOYS | 14 | 24 |
| 689 | 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 |
| 690 | 1 | 3 | 1238 1994 JOURNAL OF MEDICAL GENETICS 31(3):260-261 GILLESSENKAESBACH G; HORSTHEMKE B CLINICAL AND MOLECULAR STUDIES IN FRAGILE-X PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 691 | 17 | 25 | 1002 1992 MEDICINA CLINICA 98(4):121-124 GINE R; ESPINAS ML; ANTICH J; CARBALLO M MOLECULAR-GENETICS OF THE FRAGILE-X SYNDROME - MOLECULAR DIAGNOSIS BY DNA PROBES | 1 | 1 |
| 692 | 0 | 2 | 2045 2001 MONATSSCHRIFT KINDERHEILKUNDE 149(3):264-264 Gladtke E Trimethoprim in the fragile X syndrome? | 0 | 0 |
| 693 | 15 | 28 | 2225 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 117A(1):21-29 Glaser B; Hessl D; Dyer-Friedman J; Johnston C; Wisbeck J; Taylor A; Reiss A Biological and environmental contributions to adaptive behavior in fragile X syndrome | 0 | 4 |
| 694 | 10 | 20 | 1750 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):226-228 Glaser D; Wohrle D; Salat U; Vogel W; Steinbach P; Mucke J Mitotic behavior of expanded CGG repeats studied on cultured cells: Further evidence for methylation-mediated triplet repeat stability in fragile X syndrome | 4 | 7 |
| 695 | 0 | 0 | 772 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):338-338 GLASS IA; DELMASTRO RG; LANYON WG; RAEBURN JA; KILPATRICK MW; CONNER JM IDENTIFICATION OF DIAGNOSTIC DNA MARKERS FOR THE FRAGILE-X SYNDROME | 0 | 0 |
| 696 | 17 | 38 | 951 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(6):1050-1056 GLASS IA; DELMASTRO RG; LANYON WG; RAEBURN JA; KILPATRICK MW; WEBB TP; CONNOR JM TIGHTLY LINKED POLYMORPHIC MARKERS FOR FRAGILE X-SYNDROME AND PRENATAL CYTOGENETIC DIAGNOSTIC EXPERIENCE | 0 | 0 |
| 697 | 16 | 47 | 789 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):298-304 GLASS IA; PIRRIT LA; WHITE EM; BELL MV; DAVIES KE; COCKBURN F; CONNOR JM LINKAGE ANALYSIS IN THE FRAGILE-X SYNDROME USING MULTIPLE DISTAL XQ POLYMORPHIC DNA MARKERS | 2 | 2 |
| 698 | 0 | 0 | 710 1990 JOURNAL OF MEDICAL GENETICS 27(3):208-208 GLASS IA; WHITE EM; PIRRIT LA; BELL MV; CONNOR JM LINKAGE STUDY OF F8 IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 699 | 0 | 0 | 1339 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):363-366 Glass L Females with fragile X: A parent's perspective | 0 | 0 |
| 700 | 5 | 18 | 2057 2001 REVISTA DE NEUROLOGIA 33:S6-S9 Glover G; Bernabe MJ; Carbonell P Gnosis of fragile X syndrome | 0 | 0 |
Page 7: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
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