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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by NCR.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1001 | 9 | 19 | 644 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(2):343-347 HO HH; KALOUSEK DK BRIEF REPORT - FRAGILE X-SYNDROME IN AUTISTIC BOYS | 10 | 14 |
| 1002 | 8 | 19 | 659 1989 PEDIATRICS 83(4):547-552 SIMKO A; HORNSTEIN L; SOUKUP S; BAGAMERY N FRAGILE X-SYNDROME - RECOGNITION IN YOUNG-CHILDREN | 28 | 31 |
| 1003 | 12 | 19 | 782 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):251-255 NOLIN SL; SNIDER DA; JENKINS EC; BROWN WT; KRAWCZUN M; STETKA D; HOUCK G; DOBKIN CS; STRONG G; SMITHDOBRANSKY G; VICTOR A; HUGHES K; KIMPTON D; LITTLE A; NAGARAJA U; KENEFICK B; SULLIVAN C FRAGILE-X SCREENING-PROGRAM IN NEW-YORK-STATE | 18 | 24 |
| 1004 | 3 | 19 | 821 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):498-502 COHEN IL; VIETZE PM; SUDHALTER V; JENKINS EC; BROWN WT EFFECTS OF AGE AND COMMUNICATION LEVEL ON EYE CONTACT IN FRAGILE-X MALES AND NON-FRAGILE-X AUTISTIC MALES | 22 | 33 |
| 1005 | 8 | 19 | 905 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(6):835-838 RAMOS FJ; EMANUEL BS; SPINNER NB FREQUENCY OF THE COMMON FRAGILE SITE AT XQ27.2 UNDER CONDITIONS OF THYMIDYLATE STRESS - IMPLICATIONS FOR CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 1 |
| 1006 | 12 | 19 | 923 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):155-160 JENKINS EC; DUNCAN CJ; GU H; GENOVESE M; KRAWCZUN MS DIALYZED FETAL BOVINE SERUM INCREASES CYTOGENETIC FRAGILE-X EXPRESSION | 1 | 1 |
| 1007 | 16 | 19 | 932 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):197-207 ROUSSEAU F; HEITZ D; BIANCALANA V; OBERLE I; MANDEL JL ON SOME TECHNICAL ASPECTS OF DIRECT DNA DIAGNOSIS OF THE FRAGILE-X SYNDROME | 27 | 46 |
| 1008 | 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 |
| 1009 | 8 | 19 | 1003 1992 MEDICINA CLINICA 98(4):131-133 PRIETO F; MARTINEZCASTELLANO F THE FRAGILE-X SYNDROME AND ITS RELATION WITH OTHER SYNDROMES LINKED TO CHROMOSOME-X ASSOCIATED WITH MENTAL-RETARDATION | 0 | 0 |
| 1010 | 15 | 19 | 1179 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):458-462 TURNER AM; ROBINSON H; WAKE S; LAING SJ; LEIGH D; TURNER G COUNSELING RISK FIGURES FOR FRAGILE-X CARRIER FEMALES OF VARYING BAND SIZES FOR USE IN PREDICTING THE LIKELIHOOD OF RETARDATION IN THEIR OFFSPRING | 5 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1011 | 13 | 19 | 1217 1994 HUMAN GENETICS 94(5):479-483 HAATAJA R; VAISANEN ML; LI MY; RYYNANEN M; LEISTI J THE FRAGILE-X SYNDROME IN FINLAND - DEMONSTRATION OF A FOUNDER EFFECT BY ANALYSIS OF MICROSATELLITE HAPLOTYPES | 11 | 19 |
| 1012 | 18 | 19 | 1300 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(4):302-306 MUELLER OT; HARTSFIELD JK; AMAR MJA; GALLARDO LA; KOUSSEFF BG FRAGILE-X SYNDROME - DISCORDANT LEVELS OF CGG REPEAT MOSAICISM IN 2 BROTHERS | 2 | 5 |
| 1013 | 11 | 19 | 1308 1995 ARCHIVES OF MEDICAL RESEARCH 26:S77-S83 DiazGallardo MY; BarrosNunez P; Diaz CA; Hernandez A; GomezEspinel I; Leal CA; Fragoso R; Figuera L; GarciaCruz D; RamirezDuenas ML; Cantu JM Molecular characterization of the fragile-X syndrome in the Mexican population | 2 | 4 |
| 1014 | 15 | 19 | 1393 1996 ACTA BIOCHIMICA POLONICA 43(2):383-388 Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; Bocian E; Halley DJJ; Horst J; Mazurczak T Analysis of unstable DNA sequence in FRM1 gene in Polish families with fragile X syndrome | 0 | 0 |
| 1015 | 14 | 19 | 1444 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):404-407 Kambouris M; Snow K; Thibodeau S; Bluhm D; Green M; Feldman GL Segregation of the fragile X mutation from a male with a full mutation: Unusual somatic instability in the FMR-1 locus | 1 | 3 |
| 1016 | 11 | 19 | 1587 1997 GENETIC TESTING 1(3):151-155 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; Prior TW; Popovich B; Rosser L; Arinami T; Ledbetter DH Methylation analysis of the fragile X syndrome by PCR | 2 | 3 |
| 1017 | 14 | 19 | 1591 1997 HUMAN GENETICS 100(5-6):564-568 Larsen LA; Gronskov K; NorgaardPedersen B; BrondumNielsen K; Hasholt L; Vuust J High-throughput analysis of fragile X (CGG)(n) alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis | 5 | 23 |
| 1018 | 5 | 19 | 1868 2000 ANNALS OF SAUDI MEDICINE 20(1):16-19 Al Husain M; Salih MAM; Zaki OK; Al Othman L; Al Nasser MN A clinical study of mentally retarded children with fragile X syndrome in Saudi Arabia | 0 | 0 |
| 1019 | 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 |
| 1020 | 3 | 19 | 2063 2001 REVISTA DE NEUROLOGIA 33:S32-S36 Goldson E Sensory integration and fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1021 | 11 | 19 | 2327 2004 EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY 112(2):189-191 Bussani C; Papi L; Sestini R; Baldinotti F; Bucciantini S; Bruni V; Scarselli G Premature ovarian failure and fragile X premutation: a study on 45 women | 0 | 0 |
| 1022 | 0 | 18 | 37 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(2):286-293 UCHIDA IA; JOYCE EM ACTIVITY OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 0 | 66 |
| 1023 | 4 | 18 | 242 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(5):947-955 CANTU ES; NUSSBAUM RL; AIRHART SD; LEDBETTER DH FRAGILE (X) EXPRESSION INDUCED BY FUDR IS TRANSIENT AND INVERSELY RELATED TO LEVELS OF THYMIDYLATE SYNTHASE ACTIVITY | 3 | 5 |
| 1024 | 6 | 18 | 263 1985 CLINICAL GENETICS 27(5):463-467 GUSTAVSON KH; DAHLBOM K; FLOOD A; HOLMGREN G; BLOMQUIST HK; SANNER G EFFECT OF FOLIC-ACID TREATMENT IN THE FRAGILE X-SYNDROME | 10 | 14 |
| 1025 | 8 | 18 | 318 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):111-126 PARTINGTON MW FEMALE RELATIVES IN FAMILIES WITH THE FRAGILE X-SYNDROME | 4 | 7 |
| 1026 | 3 | 18 | 322 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):189-194 LOEHR JP; SYNHORST DP; WOLFE RR; HAGERMAN RJ AORTIC ROOT DILATATION AND MITRAL-VALVE PROLAPSE IN THE FRAGILE-X SYNDROME | 19 | 28 |
| 1027 | 6 | 18 | 337 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):403-408 WAHLSTROM J; GILLBERG C; GUSTAVSON KH; HOLMGREN G INFANTILE-AUTISM AND THE FRAGILE-X - A SWEDISH MULTICENTER STUDY | 23 | 44 |
| 1028 | 4 | 18 | 345 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):537-544 NIELSEN KB SEX-CHROMOSOME ANEUPLOIDY IN FRAGILE-X CARRIERS | 1 | 6 |
| 1029 | 0 | 18 | 372 1986 CLINICAL ENDOCRINOLOGY 24(3):327-333 OHARE JP; OBRIEN IAD; ARENDT J; ASTLEY P; RATCLIFFE W; ANDREWS H; WALTERS R; CORRALL RJM DOES MELATONIN DEFICIENCY CAUSE THE ENLARGED GENITALIA OF THE FRAGILE-X SYNDROME | 9 | 11 |
| 1030 | 8 | 18 | 390 1986 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 7(4):253-256 MADISON LS; WELLS TE; FRISTO TE; BENESCH CG A CONTROLLED-STUDY OF FOLIC-ACID TREATMENT IN 3 FRAGILE-X SYNDROME MALES | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1031 | 4 | 18 | 476 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:73-79 PUESCHEL SM; OBRIEN MM; PADREMENDOZA T KLINEFELTER SYNDROME AND ASSOCIATED FRAGILE-X SYNDROME | 7 | 8 |
| 1032 | 0 | 18 | 510 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):77-82 PHELAN MC; STEVENSON RE; COLLINS JL; TRENT HE FRAGILE-X SYNDROME AND NEOPLASIA | 7 | 13 |
| 1033 | 4 | 18 | 542 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):613-623 WARREN ST; ZHANG F; SUTCLIFFE JS; PETERS JF STRATEGY FOR MOLECULAR-CLONING OF THE FRAGILE-X SITE DNA | 7 | 12 |
| 1034 | 7 | 18 | 616 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(1):92-99 BRIDGE PJ; LILLICRAP DP MOLECULAR DIAGNOSIS OF THE FRAGILE-X [FRA-(X)] SYNDROME - CALCULATION OF RISKS BASED ON FLANKING DNA MARKERS IN SMALL PHASE-UNKNOWN FAMILIES | 0 | 4 |
| 1035 | 3 | 18 | 731 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; ZHANG FP ISOLATION OF THE HUMAN CHROMOSOMAL BAND XQ28 WITHIN SOMATIC-CELL HYBRIDS BY FRAGILE X-SITE BREAKAGE | 24 | 69 |
| 1036 | 6 | 18 | 794 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):328-331 VANOOST BA; SMITS A; DREESEN JCFM; SMEETS D; PERDON L; VANBENNEKOM CA; DAHL N; BAKKER E; OOSTRA BA MULTIPOINT LINKAGE ANALYSIS OF DXS369 AND DXS304 IN FRAGILE-X FAMILIES | 4 | 7 |
| 1037 | 12 | 18 | 799 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):367-369 PELLISSIER MC; VOELCKEL MA; PIQUET C; MATTEI MG; MATTEI JF TRANSMISSION OF MENTAL-RETARDATION WITH FRAGILE-X SITE BY 2 NORMAL TRANSMITTER BROTHERS | 0 | 0 |
| 1038 | 9 | 18 | 877 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):831-834 HILTON DK; MARTIN CA; HEFFRON WM; HALL BD; JOHNSON GL IMIPRAMINE TREATMENT OF ADHD IN A FRAGILE-X CHILD | 4 | 9 |
| 1039 | 10 | 18 | 910 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):56-60 EINFELD S; HALL W BEHAVIOR PHENOTYPE OF THE FRAGILE X SYNDROME | 6 | 12 |
| 1040 | 11 | 18 | 913 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):72-77 LACHIEWICZ AM ABNORMAL BEHAVIORS OF YOUNG GIRLS WITH FRAGILE-X SYNDROME | 20 | 27 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1041 | 13 | 18 | 981 1992 HUMAN GENETICS 89(1):114-116 WOHRLE D; HIRST MC; KENNERKNECHT I; DAVIES KE; STEINBACH P GENOTYPE MOSAICISM IN FRAGILE-X FETAL TISSUES | 32 | 43 |
| 1042 | 17 | 18 | 1186 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):490-496 MADDALENA A; HICKS BD; SPENCE WC; LEVINSON G; HOWARDPEEBLES PN PRENATAL-DIAGNOSIS IN KNOWN FRAGILE-X CARRIERS | 7 | 12 |
| 1043 | 7 | 18 | 1223 1994 INTELLIGENCE 19(1):45-50 DANIELS JK; OWEN MJ; MCGUFFIN P; THOMPSON L; DETTERMAN DK; CHORNEY M; CHORNEY K; SMITH D; SKUDER P; VIGNETTI S; MCCLEARN GE; PLOMIN R IQ AND VARIATION IN THE NUMBER OF FRAGILE-X CGG REPEATS - NO ASSOCIATION IN A NORMAL SAMPLE | 2 | 9 |
| 1044 | 15 | 18 | 1244 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(9):1316-1321 MERENSTEIN SA; SHYU V; SOBESKY WE; STALEY L; BERRYKRAVIS E; NELSON DL; LUGENBEEL KA; TAYLOR AK; PENNINGTON BF; HAGERMAN RJ FRAGILE-X SYNDROME IN A NORMAL IQ MALE WITH LEARNING AND EMOTIONAL-PROBLEMS | 18 | 22 |
| 1045 | 7 | 18 | 1342 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):396-404 Mazzocco MMM; Lachiewicz AM; Kovar CG; Freund LS; Baumgardner TL; Dykens E Psychological and emotional studies of the fragile X mutation - A workshop summary | 0 | 0 |
| 1046 | 2 | 18 | 1390 1995 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 92(11):5199-5203 CHEN XA; MARIAPPAN SVS; CATASTI P; RATLIFF R; MOYZIS RK; LAAYOUN A; SMITH SS; BRADBURY EM; GUPTA G HAIRPINS ARE FORMED BY THE SINGLE DNA STRANDS OF THE FRAGILE-X TRIPLET REPEATS - STRUCTURE AND BIOLOGICAL IMPLICATIONS | 25 | 154 |
| 1047 | 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 |
| 1048 | 3 | 18 | 1443 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):395-398 Piussan C; Mathieu M; Berquin P; Fryns JP Fragile X mutation and FG syndrome-like phenotype | 1 | 4 |
| 1049 | 10 | 18 | 1770 1999 AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY 33(3):436-440 Al-Semaan Y; Malla AK; Lazosky A Schizoaffective disorder in a fragile-X carrier | 0 | 0 |
| 1050 | 7 | 18 | 1798 1999 JOURNAL OF CHILD NEUROLOGY 14(2):108-112 Singh R; Sutherland GR; Manson J Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1051 | 12 | 18 | 1808 1999 JOURNAL OF MEDICAL GENETICS 36(3):253-257 Helderman-van den Enden ATJM; Maaswinkel-Mooij PD; Hoogendoorn E; Willemsen R; Maat-Kievit JA; Losekoot M; Oostra BA Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities | 3 | 8 |
| 1052 | 3 | 18 | 1878 2000 CHINESE SCIENCE BULLETIN 45(6):516-520 Chen YT; Bardoni B; Yu M; Zhu N; Wu GY; Mandel JL; Shen Y Fragile X mental retardation protein interacts with TDG | 0 | 0 |
| 1053 | 0 | 18 | 1886 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12(1):381-384 Miller WJ; Skinner JA; Foss GS; Davies KE Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain | 0 | 7 |
| 1054 | 8 | 18 | 1956 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):265-277 Bakker CE; Kooy RF; D'Hooge R; Tamanini F; Willemsen R; Nieuwenhuizen I; De Vries BBA; Reyniers E; Hoogeveen AT; Willems PJ; De Deyn PP; Oostra BA Introduction of a FMR1 transgene in the fragile X knockout mouse. | 3 | 3 |
| 1055 | 7 | 18 | 1984 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):110-115 Stoll C Problems in the diagnosis of fragile X syndrome in young children are still present | 3 | 3 |
| 1056 | 5 | 18 | 2057 2001 REVISTA DE NEUROLOGIA 33:S6-S9 Glover G; Bernabe MJ; Carbonell P Gnosis of fragile X syndrome | 0 | 0 |
| 1057 | 9 | 18 | 2094 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 107(2):136-142 Loesch DZ; Huggins RM; Taylor AK Application of robust pedigree analysis in studies of complex genotype-phenotype relationships in fragile X syndrome | 5 | 6 |
| 1058 | 6 | 18 | 2113 2002 CLINICAL GENETICS 61(1):13-20 O'Connell CD; Atha DH; Jakupciak JP; Richie KI Standardization of PCR amplification for fragile X trinucleotide repeat measurements | 0 | 3 |
| 1059 | 11 | 18 | 2223 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(2):176-178 Stalker HJ; Keller KL; Gray BA; Zori RT Concurrence of fragile X syndrome and 47, XYY in an individual with a Prader-Willi-Like phenotype | 0 | 0 |
| 1060 | 1 | 17 | 18 1981 HUMAN GENETICS 59(2):166-169 MATTEI MG; MATTEI JF; VIDAL I; GIRAUD F EXPRESSION IN LYMPHOCYTE AND FIBROBLAST-CULTURE OF THE FRAGILE X-CHROMOSOME - A NEW TECHNICAL APPROACH | 44 | 83 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1061 | 9 | 17 | 113 1983 ANNALES DE GENETIQUE 26(4):247-250 TEJADA I; BOUE J; GILGENKRANTZ S PRENATAL-DIAGNOSIS OF FRAGILE X-CHROMOSOME ON AMNIOTIC-FLUID CELLS | 6 | 9 |
| 1062 | 5 | 17 | 135 1983 HUMAN GENETICS 64(2):148-150 NUSSBAUM RL; AIRHART SD; LEDBETTER DH EXPRESSION OF THE FRAGILE (X)CHROMOSOME IN AN INTERSPECIFIC SOMATIC-CELL HYBRID | 18 | 58 |
| 1063 | 8 | 17 | 149 1983 JOURNAL OF MENTAL DEFICIENCY RESEARCH 27(SEP):211-226 NIELSEN KB DIAGNOSIS OF THE FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) - CLINICAL FINDINGS IN 27 MALES WITH THE FRAGILE SITE AT XQ28 | 18 | 26 |
| 1064 | 6 | 17 | 239 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(1):193-198 ABRUZZO MA; MAYER M; JACOBS PA THE EFFECT OF METHIONINE AND 5-AZACYTIDINE ON FRAGILE-X EXPRESSION | 3 | 5 |
| 1065 | 2 | 17 | 286 1985 HUMAN GENETICS 69(4):327-331 MATTEI MG; BAETEMAN MA; HEILIG R; OBERLE I; DAVIES K; MANDEL JL; MATTEI JF LOCALIZATION BY INSITU HYBRIDIZATION OF THE COAGULATION FACTOR-IX GENE AND OF 2 POLYMORPHIC DNA PROBES WITH RESPECT TO THE FRAGILE-X SITE | 8 | 49 |
| 1066 | 5 | 17 | 292 1985 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 15(3):335-338 PUESCHEL SM; HERMAN R; GRODEN G SCREENING-CHILDREN WITH AUTISM FOR FRAGILE-X SYNDROME AND PHENYLKETONURIA | 15 | 25 |
| 1067 | 5 | 17 | 311 1985 TRENDS IN GENETICS 1(4):108-112 SUTHERLAND GR THE ENIGMA OF THE FRAGILE-X CHROMOSOME | 26 | 43 |
| 1068 | 4 | 17 | 316 1986 AMERICAN JOURNAL OF HUMAN GENETICS 38(4):533-539 ABRUZZO MA; HUNT PA; MAYER M; JACOBS PA; WANG JCC; ERBE RW A COMPARISON OF FRAGILE X-EXPRESSION IN LYMPHOCYTE AND LYMPHOBLASTOID CULTURES | 2 | 3 |
| 1069 | 2 | 17 | 325 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):227-239 BERKOVITZ GD; WILSON DP; CARPENTER NJ; BROWN TR; MIGEON CJ GONADAL-FUNCTION IN MEN WITH THE MARTIN-BELL (FRAGILE-X) SYNDROME | 10 | 14 |
| 1070 | 9 | 17 | 327 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):263-271 BROWN WT; COHEN IL; FISCH GS; WOLFSCHEIN EG; JENKINS VA; MALIK MN; JENKINS EC HIGH-DOSE FOLIC-ACID TREATMENT OF FRAGILE-(X) MALES | 9 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1071 | 7 | 17 | 419 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 28(1):13-15 CHUDLEY AE; DEVONFLINDT R; HAGERMAN RJ COGNITIVE VARIABILITY IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 1072 | 4 | 17 | 421 1987 AMERICAN JOURNAL OF MENTAL DEFICIENCY 92(2):234-236 DYKENS EM; HODAPP RM; LECKMAN JF STRENGTHS AND WEAKNESSES IN THE INTELLECTUAL-FUNCTIONING OF MALES WITH FRAGILE-X SYNDROME | 24 | 44 |
| 1073 | 2 | 17 | 552 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(2):407-414 REISS AL; PATEL S; KUMAR AJ; FREUND L PRELIMINARY COMMUNICATION - NEUROANATOMICAL VARIATIONS OF THE POSTERIOR-FOSSA IN MEN WITH THE FRAGILE-X (MARTIN-BELL) SYNDROME | 16 | 38 |
| 1074 | 2 | 17 | 586 1988 HUMAN GENETICS 79(3):231-234 JOHANNISSON R; FROSTERISKENIUS U; SAADALLAH N; HULTEN MA SPERMATOGENESIS IN 2 PATIENTS WITH THE FRAGILE-X SYNDROME .2. 1ST MEIOSIS - LIGHT AND ELECTRON-MICROSCOPY | 1 | 3 |
| 1075 | 5 | 17 | 605 1988 JOURNAL OF MEDICAL GENETICS 25(6):407-414 LOESCH DZ; HAY DA CLINICAL-FEATURES AND REPRODUCTIVE PATTERNS IN FRAGILE-X FEMALE HETEROZYGOTES | 33 | 43 |
| 1076 | 2 | 17 | 627 1989 ARCHIVES OF NEUROLOGY 46(12):1269-1270 GRIGSBY J; HAGERMAN R FRAGILE-X SYNDROME - A GENETIC ETIOLOGY FOR DEVELOPMENTAL GERSTMANN SYNDROME | 0 | 0 |
| 1077 | 10 | 17 | 642 1989 HUMAN GENETICS 82(1):79-81 SCHAAP T THE ROLE OF RECOMBINATION IN THE EVOLVEMENT OF THE FRAGILE X-MUTATION | 2 | 2 |
| 1078 | 6 | 17 | 680 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(2):265-267 MOORE PSJ; CHUDLEY AE; WINTER JSD TRUE PRECOCIOUS PUBERTY IN A GIRL WITH THE FRAGILE X-SYNDROME | 10 | 13 |
| 1079 | 7 | 17 | 733 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(1):108-116 ROUSSEAU F; VINCENT A; RIVELLA S; HEITZ D; TRIBOLI C; MAESTRINI E; WARREN ST; SUTHERS GK; GOODFELLOW P; MANDEL JL; TONIOLO D; OBERLE I 4 CHROMOSOMAL BREAKPOINTS AND 4 NEW PROBES MARK OUT A 10-CM REGION ENCOMPASSING THE FRAGILE-X LOCUS (FRAXA) | 25 | 48 |
| 1080 | 6 | 17 | 737 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(6):1051-1057 RICHARDS RI; SHEN Y; HOLMAN K; KOZMAN H; HYLAND VJ; MULLEY JC; SUTHERLAND GR FRAGILE-X SYNDROME - DIAGNOSIS USING HIGHLY POLYMORPHIC MICROSATELLITE MARKERS | 14 | 40 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1081 | 11 | 17 | 872 1991 JOURNAL OF MEDICAL GENETICS 28(12):824-829 HIRST MC; NAKAHORI Y; KNIGHT SJL; SCHWARTZ C; THIBODEAU SN; ROCHE A; FLINT TJ; CONNOR JM; FRYNS JP; DAVIES KE GENOTYPE PREDICTION IN THE FRAGILE-X SYNDROME | 27 | 36 |
| 1082 | 10 | 17 | 930 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):187-191 VERKERK AJMH; EUSSEN BHJ; VANHEMEL JO; OOSTRA BA LIMITED SIZE OF THE FRAGILE-X SITE SHOWN BY FLUORESCENCE INSITU HYBRIDIZATION | 6 | 7 |
| 1083 | 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 |
| 1084 | 12 | 17 | 1004 1992 MENTAL RETARDATION 30(6):355-361 KEENAN J; KASTNER T; NATHANSON R; RICHARDSON N; HINTON J; CRESS DA A STATEWIDE PUBLIC AND PROFESSIONAL-EDUCATION PROGRAM ON FRAGILE X SYNDROME | 0 | 2 |
| 1085 | 7 | 17 | 1014 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 | 47 | 78 |
| 1086 | 5 | 17 | 1072 1993 BIOLOGICAL PSYCHIATRY 33(3):213-216 JEFFRIES FM; REISS AL; BROWN WT; MEYERS DA; GLICKSMAN AC; BANDYOPADHYAY S BIPOLAR SPECTRUM DISORDER AND FRAGILE-X SYNDROME - A FAMILY STUDY | 4 | 13 |
| 1087 | 8 | 17 | 1132 1993 NATURE 363(6431):722-724 VERHEIJ C; BAKKER CE; DEGRAAFF E; KEULEMANS J; WILLEMSEN R; VERKERK AJMH; GALJAARD H; REUSER AJJ; HOOGEVEEN AT; OOSTRA BA CHARACTERIZATION AND LOCALIZATION OF THE FMR-1 GENE-PRODUCT ASSOCIATED WITH FRAGILE-X SYNDROME | 103 | 182 |
| 1088 | 15 | 17 | 1173 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):428-435 KOLEHMAINEN K POPULATION-GENETICS OF FRAGILE-X - A MULTIPLE ALLELE MODEL WITH VARIABLE RISK OF CGG REPEAT EXPANSION | 15 | 21 |
| 1089 | 16 | 17 | 1189 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):509-512 NOLIN SL; GLICKSMAN A; HOUCK GE; BROWN WT; DOBKIN CS MOSAICISM IN FRAGILE-X AFFECTED MALES | 36 | 40 |
| 1090 | 14 | 17 | 1194 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):370-373 PUISSANT H; MALINGE MC; LARGETPIET A; MARTIN D; CHAUVEAU P; ODENT S; PLESSIS G; PARENT P; LEMAREC B; LARGETPIET L MOLECULAR ANALYSIS OF 53 FRAGILE-X FAMILIES WITH THE PROBE-STB12.3 | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1091 | 14 | 17 | 1509 1996 PEDIATRICS 98(2):297-300 Desposito F; Cho S; Frias JL; Sherman J; Wappner RS; Wilson MG Health supervision for children with fragile X syndrome | 3 | 8 |
| 1092 | 11 | 17 | 1942 2000 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 99(5):402-407 Wang YC; Li C; Lin ML; Lin WH; Li SY Molecular diagnosis of fragile X syndrome and distribution of CGG repeats in the FMR-1 gene in Taiwanese | 0 | 0 |
| 1093 | 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 |
| 1094 | 16 | 17 | 2006 2001 CELL 107(5):555-557 Kaytor MD; Orr HT RNA targets of the fragile X protein | 5 | 13 |
| 1095 | 11 | 17 | 2042 2001 MEDICAL PRINCIPLES AND PRACTICE 10(2):73-78 Alkhalaf M; Verghese L; Mushtaq SK Cytogenetic and immunohistochemical characterization of fragile X syndrome in a Kuwaiti family: Rapid antibody test for the diagnosis of mental retardation patients | 0 | 0 |
| 1096 | 4 | 16 | 170 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):111-121 HAGERMAN RJ; VANHOUSEN K; SMITH ACM; MCGAVRAN L CONSIDERATION OF CONNECTIVE-TISSUE DYSFUNCTION IN THE FRAGILE-X SYNDROME | 25 | 35 |
| 1097 | 2 | 16 | 172 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):159-174 MERYASH DL; CRONK CE; SACHS B; GERALD PS AN ANTHROPOMETRIC STUDY OF MALES WITH THE FRAGILE-X SYNDROME | 26 | 43 |
| 1098 | 4 | 16 | 177 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):241-252 SOUDEK D; PARTINGTON MW; LAWSON JS THE FRAGILE-X SYNDROME .1. FAMILIAL VARIATION IN THE PROPORTION OF LYMPHOCYTES WITH THE FRAGILE SITE IN MALES | 24 | 29 |
| 1099 | 6 | 16 | 231 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 |
| 1100 | 8 | 16 | 340 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):467-473 KRAWCZUN MS; LELE KP; JENKINS EC; BROWN WT FRAGILE-X EXPRESSION INCREASED BY LOW CELL-CULTURE DENSITY | 5 | 8 |
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