| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by LCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1501 | 0 | 0 | 1904 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 |
| 1502 | 9 | 29 | 1905 1999 INTERNATIONAL JOURNAL OF BEHAVIORAL DEVELOPMENT 23(2):519-531 Burack JA; Shulman C; Katzir E; Schaap T; Brennan JM; et al. Cognitive and behavioural development of Israeli males with fragile X and Down Syndrome | 1 | 1 |
| 1503 | 7 | 18 | 1908 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 |
| 1504 | 2 | 5 | 1916 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-171 Macpherson J; Murray A; Webb J; Jacobs P Fragile X syndrome: of POF and premutations | 1 | 2 |
| 1505 | 5 | 6 | 1920 1999 JOURNAL OF MEDICAL GENETICS 36(7):565-566 Moore SJ; Strain L; Cole GF; Miedzybrodzka Z; Kelly KF; et al. Fragile X syndrome with FMR1 and FMR2 deletion | 1 | 3 |
| 1506 | 4 | 4 | 1923 1999 LANCET 353(9159):1153-1154 Hong CJ; Song HL; Lai HC; Tsai SJ; Hsiao KJ Methanol/acetone treatment helps the amplification of FMR1 CGG repeat fragment in dried blood spots from Guthrie cards | 1 | 5 |
| 1507 | 0 | 0 | 1942 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Jin P; Feng Y; Brown V; Warren ST Identification of polyribosomes-associated mRNAs regulated by fragile X mental retardation protein (FMRP) using oligonucleotide microarrays. | 1 | 2 |
| 1508 | 0 | 0 | 1943 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Brown V; Ceman S; Jin P; Jin C; Wilkinson KD; et al. Messenger RNAs associated with the fragile X mental retardation protein in mouse brain. | 1 | 1 |
| 1509 | 0 | 0 | 1959 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):360-360 Ramos FJ; Mila M; Ortilles M; Rife M; Tazon B; et al. Validity of the analysis of the FMRP expression in bloodsmears as a screening method for the Fragile X Syndrome. | 1 | 1 |
| 1510 | 0 | 0 | 1963 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Raca G; Siyanova E; Mirkin S Janus effects of premutation size CGG repeats on gene expression. | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1511 | 5 | 8 | 1986 2000 AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE 30(1):86-88 Driscoll G; Clark J; Elakis G; Turner G Early menopause in a family carrying a fragile X premutation | 1 | 3 |
| 1512 | 23 | 46 | 2004 2000 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 42(11):768-774 Sheldon L; Turk J Monozygotic boys with fragile X syndrome | 1 | 2 |
| 1513 | 31 | 44 | 2016 2000 GENETICS IN MEDICINE 2(4):242-248 Burman RW; Anoe KS; Popovich BW Fragile X full mutations ave more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics | 1 | 2 |
| 1514 | 3 | 6 | 2018 2000 HUMAN GENETICS 107(2):195-196 Castellvi-Bel S; Fernandez-Burriel M; Rife M; Jimenez D; Mallolas J; et al. Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles | 1 | 3 |
| 1515 | 1 | 2 | 2028 2000 HUMAN REPRODUCTION 15(8):1874-1875 Marozzi A Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 1 | 1 |
| 1516 | 27 | 59 | 2034 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(42):33134-33141 Uliel L; Weisman-Shomer P; Oren-Jazans H; Newcomb T; Loeb LA; et al. Human Ku antigen tightly binds and stabilizes a tetrahelical form of the fragile X syndrome d(CGG)(n) expanded sequence | 1 | 7 |
| 1517 | 0 | 0 | 2046 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:317-317 Karrer JH; Hagerman RJ; Karrer RS; Fitzpatrick D; Vavold J; et al. Genotypic-specific event-related brain potentials among infants and toddlers with fragile-X syndrome and Down syndrome | 1 | 1 |
| 1518 | 4 | 15 | 2066 2000 JOURNAL OF PSYCHOEDUCATIONAL ASSESSMENT 18(3):255-267 Hooper SR; Hatton DD; Baranek GT; Roberts JP; Bailey DB Nonverbal assessment of IQ, attention, and memory abilities in children with fragile-X syndrome using the Leiter-R | 1 | 1 |
| 1519 | 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 |
| 1520 | 9 | 25 | 2141 2001 COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING 4(3):265-272 Murray J; Cuckle H Cystic fibrosis and fragile X syndrome: The arguments for antenatal screening | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1521 | 12 | 27 | 2145 2001 DIAGNOSTIC MOLECULAR PATHOLOGY 10(1):34-40 Tzeng CC; Lin SJ; Chen YJ; Kuo PL; Jong YJ; et al. An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome | 1 | 3 |
| 1522 | 13 | 17 | 2148 2001 EUROPEAN JOURNAL OF HUMAN GENETICS 9(9):724-727 Larsen LA; Vuust J; Nystad M; Evseeva I; Van Ghelue M; et al. Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia | 1 | 3 |
| 1523 | 65 | 108 | 2183 2001 MOLECULAR GENETICS AND METABOLISM 74(1-2):89-97 Hagerman RJ; Hagerman PJ Fragile X syndrome: A model of gene-brain-behavior relationships | 1 | 2 |
| 1524 | 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 |
| 1525 | 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 |
| 1526 | 16 | 28 | 2216 2002 ACTA PAEDIATRICA 91(5):535-539 Hecimovic S; Tarnik IP; Baric I; Cakarun Z; Pavelic K Screening for fragile X syndrome: results from a school for mentally retarded children | 1 | 1 |
| 1527 | 6 | 7 | 2235 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 107(4):344-345 Vink GR; Froster UG Comparison of FMR1-protein expression in lymphocytes, methylation pattern in Southern blot analysis, and IQ values in three sisters with the fragile X syndrome | 1 | 1 |
| 1528 | 30 | 43 | 2240 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(3):243-252 Mingroni-Netto RC; Angeli CB; Auricchio MTBM; Leal-Mesquita ER; Ribeiro-dos-Santos AKC; et al. Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations | 1 | 3 |
| 1529 | 8 | 44 | 2245 2002 AMERICAN JOURNAL OF OCCUPATIONAL THERAPY 56(5):538-546 Baranek GT; Chin YKH; Hess LMG; Yankee JG; Hatton DD; et al. Sensory processing correlates of occupational performance in children with fragile X syndrome: Preliminary findings | 1 | 1 |
| 1530 | 14 | 57 | 2263 2002 DEVELOPMENTAL PSYCHOBIOLOGY 41(2):133-146 Keysor CS; Mazzocco MMM; McLeod DR; Hoehn-Saric R Physiological arousal in females with fragile X or Turner syndrome | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1531 | 0 | 53 | 2292 2002 JOURNAL OF BACTERIOLOGY 184(1):177-182 Semsey S; Blaha B; Koles K; Orosz L; Papp PP Site-specific integrative elements of rhizobiophage 16-3 can integrate into proline tRNA (CGG) genes in different bacterial genera | 1 | 6 |
| 1532 | 67 | 98 | 2304 2002 JOURNAL OF NEUROSCIENCE RESEARCH 70(5):623-630 Todd PK; Malter JS Fragile X mental retardation protein in plasticity and disease | 1 | 4 |
| 1533 | 55 | 82 | 2309 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):135-144 Kaufmann WE; Cohen S; Sun HT; Ho G Molecular phenotype of fragile X syndrome: FMRP, FXRPs, and protein targets | 1 | 1 |
| 1534 | 43 | 64 | 2311 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):148-155 Hoogeveen AT; Willemsen R; Oostra BA Fragile X syndrome, the fragile X related proteins, and animal models | 1 | 4 |
| 1535 | 0 | 0 | 2321 2002 MOVEMENT DISORDERS 17:S351-S351 Leehey MA; Grigsby J; Rubinstein D; Jacquemont S; Greco C; et al. Parkinsonism, tremor and ataxia in a female fragile X carrier | 1 | 1 |
| 1536 | 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 |
| 1537 | 29 | 60 | 2386 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(5):314-326 Demark JL; Feldman MA; Holden JJA Behavioral relationship between autism and fragile X syndrome | 1 | 2 |
| 1538 | 0 | 0 | 2390 2003 ANNALS OF NEUROLOGY 54:S105-S106 Kaufmann WE; Danko CG; Kau ASM; Thevarajah S; Bukelis I; et al. Increased protein acetylation in lymphocytes predicts autistic behavior in Fragile X syndrome | 1 | 1 |
| 1539 | 15 | 55 | 2424 2003 GENETICS IN MEDICINE 5(5):378-384 Skinner D; Sparkman KL; Bailey DB Screening for fragile X syndrome: Parent attitudes and perspectives | 1 | 1 |
| 1540 | 34 | 43 | 2427 2003 HUMAN GENETICS 113(5):371-376 Arocena DG; Breece KE; Hagerman PJ Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1541 | 7 | 32 | 2443 2003 JOURNAL OF INTELLECTUAL & DEVELOPMENTAL DISABILITY 28(2):135-144 Richdale AL A descriptive analysis of sleep behaviour in children with Fragile X | 1 | 1 |
| 1542 | 28 | 41 | 2448 2003 JOURNAL OF MEDICAL GENETICS 40(7):535-539 de Vries BBA; Severijnen LA; Jacobs A; Olmer R; Halley DJJ; et al. FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics | 1 | 1 |
| 1543 | 7 | 10 | 2462 2003 NEURON 38(6):843-845 Billuart P; Chelly J From fragile X mental retardation protein to Rac1 GTPase: New insights from fly CYFIP | 1 | 2 |
| 1544 | 41 | 101 | 2465 2003 NEUROPSYCHOLOGY 17(4):646-657 Loesch DZ; Bui QM; Grigsby J; Butler E; Epstein J; et al. Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X | 1 | 1 |
| 1545 | 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 |
| 1546 | 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 |
| 1547 | 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 |
| 1548 | 2 | 10 | 2483 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):730-731 Mandel JL Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation | 1 | 1 |
| 1549 | 60 | 135 | 2506 2004 CELLULAR AND MOLECULAR LIFE SCIENCES 61(14):1714-1728 Denman RB; Dolzhanskaya N; Sung YJ Regulating a translational regulator: mechanisms cells use to control the activity of the fragile X mental retardation protein | 1 | 2 |
| 1550 | 5 | 41 | 2513 2004 DEVELOPMENTAL SCIENCE 7(1):116-130 Scerif G; Cornish K; Wilding J; Driver J; Karmiloff-Smith A Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1551 | 41 | 114 | 2519 2004 GENES BRAIN AND BEHAVIOR 3(6):337-359 Yan QJ; Asafo-Adjei PK; Arnold HM; Brown RE; Bauchwitz RP A phenotypic and molecular characterization of the fmr1-tm1Cgr Fragile X mouse | 1 | 1 |
| 1552 | 21 | 42 | 2528 2004 HUMAN MOLECULAR GENETICS 13(1):79-89 Wang HP; Ku L; Osterhout DJ; Li W; Ahmadian A; et al. Developmentally-programmed FMRP expression in oligodendrocytes: a potential role of FMRP in regulating translation in oligodendroglia progenitors | 1 | 3 |
| 1553 | 2 | 6 | 2533 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2946 Hagerman PJ; Hagerman RJ; Gane LW Genetic counseling for families of patients with fragile X syndrome - In reply | 1 | 1 |
| 1554 | 16 | 25 | 2562 2004 JOURNAL OF NEUROSCIENCE 24(47):10579-10583 Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al. Visual experience regulates transient expression and dendritic localization of Fragile X mental retardation protein | 1 | 1 |
| 1555 | 34 | 67 | 2568 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):11-16 Cornish K; Sudhalter V; Turk J Attention and language in fragile X | 1 | 1 |
| 1556 | 39 | 74 | 2569 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):17-24 Hessl D; Rivera SM; Reiss AL The neuroanatomy and neuroendocrinotogy of fragile X syndrome | 1 | 2 |
| 1557 | 39 | 66 | 2571 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):31-41 Loesch DZ; Huggins RM; Hagerman RJ Phenotypic variation and FMRP levels in fragile X | 1 | 1 |
| 1558 | 21 | 82 | 2576 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):68-74 Siomi H; Ishizuka A; Siomi MC RNA interference: A new mechanism by which FMRP acts in the normal brain? What can drosophila teach us? | 1 | 4 |
| 1559 | 11 | 11 | 2579 2004 MOLECULAR HUMAN REPRODUCTION 10(10):773-776 Rife M; Badenas C; Quinto L; Puigoriol E; Tazon B; et al. Analysis of CGG variation through 642 meioses in Fragile X families | 1 | 1 |
| 1560 | 11 | 56 | 2643 2005 NEURON 45(5):753-764 McBride SMJ; Choi CH; Wang Y; Liebelt D; Braunstein E; et al. Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1561 | 59 | 77 | 2647 2005 TRENDS IN GENETICS 21(1):37-45 Zhang YQ; Broadie K Fathoming fragile X in fruit flies | 1 | 1 |
| 1562 | 0 | 1 | 1 1967 NEW PHYTOLOGIST 66(1):138-& CORNER EJH VANSTEENIS,CGG - PACIFIC PLANT AREAS 2 | 0 | 0 |
| 1563 | 0 | 0 | 2 1976 GASTROENTEROLOGY 70(5):875-875 SILVA LCD; SETTE H; ANTONACIO F; STRASSMAN P; LOPES JD COMMERCIAL GAMMAGLOBULIN (CGG) AS A POSSIBLE VEHICLE OF TRANSMISSION OF HB-S AG IN FAMILIAL CLUSTERING | 0 | 0 |
| 1564 | 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 |
| 1565 | 0 | 1 | 4 1980 AMERICAN JOURNAL OF HUMAN GENETICS 32(6):A73-A73 JACKY PB EXPRESSION IN FIBROBLAST-CULTURE OF THE FRAGILE X-CHROMOSOME ASSOCIATED WITH FAMILIAL SEX-LINKED MENTAL-RETARDATION - FACTORS INFLUENCING A RELIABLE DETERMINATION OF THE FREQUENCY OF EXPRESSION | 0 | 0 |
| 1566 | 0 | 0 | 13 1981 ANGLO-WELSH REVIEW (68):6-9 WESTLEY M 'FRAGILE-X' | 0 | 0 |
| 1567 | 0 | 0 | 20 1981 CLINICAL RESEARCH 29(1):A134-A134 HERBST DS; GERRARD JW; DUNN HG; DILL FJ; KALOUSEK DK; et al. NONSPECIFIC X-LINKED MENTAL-RETARDATION, MACRO-ORCHIDISM AND THE FRAGILE X-CHROMOSOME MARKER | 0 | 0 |
| 1568 | 1 | 7 | 32 1981 LYON MEDICAL 246(20):428-429 [Anon] MENTAL-RETARDATION DUE TO A FRAGILE X-CHROMOSOME | 0 | 0 |
| 1569 | 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 |
| 1570 | 0 | 18 | 40 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(2):286-293 UCHIDA IA; JOYCE EM ACTIVITY OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 0 | 66 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1571 | 0 | 0 | 54 1982 BEHAVIOR GENETICS 12(6):599-599 THEOBALD TM; HAY DA BEHAVIORAL-CORRELATES OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 1572 | 0 | 0 | 56 1982 CLINICAL RESEARCH 30(2):A291-A291 BROWN WT; JENKINS EC; FRIEDMAN E; WISNIEWSKI K; FRENCH JH THE FRAGILE X-SYNDROME - A GENETIC CAUSE OF AUTISM | 0 | 0 |
| 1573 | 0 | 0 | 58 1982 CLINICAL RESEARCH 30(5):A890-A890 KRUMDIECK CL; HOWARDPEEBLES PN THE ORIGIN OF THE FRAGILE X IN HUMAN-CHROMOSOMES - AN HYPOTHESIS | 0 | 0 |
| 1574 | 0 | 0 | 74 1982 JOURNAL OF MEDICAL GENETICS 19(1):64-64 DAKER MG; CHIDIAC P; FEAR CN; BERRY AC FRAGILE X-CHROMOSOME IN BROTHERS WITH NORMAL INTELLIGENCE, OR THE MAN WHO MIGHT HAVE BEEN A GENIUS | 0 | 2 |
| 1575 | 0 | 0 | 75 1982 JOURNAL OF MEDICAL GENETICS 19(5):371-371 WILLATT LR; DAVIS J FRAGILE-X MENTAL-RETARDATION IN TWINS - A CASE-HISTORY | 0 | 0 |
| 1576 | 0 | 0 | 91 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A81-A81 BROWN T; JENKINS E; SHAPIRO LR FRAGILE (X) SYNDROME PRENATAL-DIAGNOSIS REGISTRY | 0 | 0 |
| 1577 | 0 | 1 | 92 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A82-A82 CARPENTER NJ; BARBER DH; JONES M; LINDLEY W; CARR C CONTROLLED 6-MONTH STUDY OF ORAL FOLIC-ACID THERAPY IN BOYS WITH FRAGILE X-LINKED MENTAL-RETARDATION | 0 | 9 |
| 1578 | 0 | 0 | 94 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A117-A117 SHAPIRO LR; SUMMA GM; WILMOT PL; GLOTH E SCREENING AND DETECTION OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 1579 | 0 | 0 | 98 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A135-A135 HOWARDPEEBLES PN FRAGILE X-CHROMOSOME - TECHNICAL ASPECTS FOR MAXIMIZING EXPRESSION | 0 | 0 |
| 1580 | 0 | 0 | 99 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A136-A136 JENKINS E; DUNCAN C; BROOKS J; LELE K; SANZ M; et al. LOW-FREQUENCY FRAGILE X-CHROMOSOMES IN CULTURES FROM NORMAL PEOPLE | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1581 | 0 | 0 | 100 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A139-A139 KNOLL JH; CHUDLEY AE; GERRARD JW FREQUENCY AND REPLICATION PATTERN OF FRAGILE (X) (Q28) IN HETEROZYGOTES | 0 | 0 |
| 1582 | 0 | 2 | 101 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A144-A144 MIXON C; DEV VG INHIBITION OF FRAGILE-X EXPRESSION BY 5-AZACYTIDINE (AZA) AND BY S-ADENOSYLHOMOCYSTEINE (SAH) | 0 | 0 |
| 1583 | 0 | 0 | 103 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A159-A159 WANG JC; BEARDSLEY GP; ERBE RW THYMIDYLATE METABOLISM AND URACIL MISINCORPORATION IN FRAGILE-X SYNDROME CELLS | 0 | 2 |
| 1584 | 0 | 0 | 104 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A161-A161 WILLEY A; HATCHER N; HEALY N FRAGILE-X FAMILIES - GENETIC INSTABILITY, OR UNEXPECTED CYTOGENETIC ABERRATIONS | 0 | 0 |
| 1585 | 0 | 0 | 105 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A162-A162 WILSON MG; MARCHESE CA; LIN MS; HERBERT WS; PERDELWITZ M PRENATAL-DIAGNOSIS OF FRAGILE-X IN A HETEROZYGOUS FEMALE FETUS AND POSTNATAL FOLLOW-UP | 0 | 0 |
| 1586 | 0 | 0 | 106 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A174-A174 HOLDEN J; BECKETT J; MULLIGAN L; PHILLIPS A; SIMPSON N; et al. A SEARCH FOR RESTRICTION FRAGMENT LENGTH POLYMORPHISMS (RFLPS) LINKED TO THE FRAGILE-X FORM OF X-LINKED MENTAL-RETARDATION | 0 | 3 |
| 1587 | 0 | 1 | 118 1983 BIOLOGY OF THE CELL 48(2-3):A92-A92 LENOARD C; SCHOEVAERT D; SELVA J APPLICATION OF THE AUTOMATIC-ANALYSIS OF METAPHASES TO THE DIAGNOSIS OF THE FRAGILE-X IN MAN | 0 | 0 |
| 1588 | 0 | 0 | 120 1983 CLINICAL GENETICS 23(3):216-216 MCDERMOTT A MORE ON THE FRAGILE-X, WITH PARTICULAR REFERENCE TO FIBROBLAST AND AMNIOTIC-FLUID CULTURE, AND X-INACTIVATION | 0 | 0 |
| 1589 | 0 | 0 | 127 1983 CLINICAL GENETICS 23(3):255-255 VERSCHRAEGENSPAE MR; VANDENBOSSCHE H; MATTON MT APPROACH TO RELATIVES IN FRAGILE X-LINKED MENTAL-RETARDATION | 0 | 2 |
| 1590 | 3 | 11 | 130 1983 CLINICAL GENETICS 24(3):153-155 NIELSEN KB; TOMMERUP N; FRIIS B; HJELT K; HIPPE E FOLIC-ACID METABOLISM IN A PATIENT WITH FRAGILE-X | 0 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1591 | 0 | 1 | 134 1983 CLINICAL RESEARCH 31(2):A290-A290 BROWN T; JENKINS E; FRIEDMAN E; BROOKS J; DUNCAN C; et al. FOLIC-ACID THERAPY OF FRAGILE-X SYNDROME | 0 | 0 |
| 1592 | 0 | 1 | 135 1983 CLINICAL RESEARCH 31(5):A897-A897 HOWARDPEEBLES PN NORMAL-MALE TRANSMISSION OF THE FRAGILE-X - THE COUNSELING DILEMMA | 0 | 0 |
| 1593 | 3 | 10 | 143 1983 JOURNAL DE GENETIQUE HUMAINE 31(2):133-139 JALBERT H; BAETEMAN MA; TROCHETROYER C; MATTEI MG; MATTEI JF; et al. MENTAL-RETARDATION WITH FRAGILE-X - NEITHER INACTIVATION NOR DELETION OF THE SEGMENT Q28-]Q TER ENZYMATIC AND MORPHOMETRIC DATA | 0 | 0 |
| 1594 | 3 | 9 | 149 1983 JOURNAL OF MEDICAL GENETICS 20(4):314-315 HUNTER AGW; MACDONALD J; EVANS JA ABSENCE OF THE FRAGILE-X IN A GROUP OF PATIENTS WITH IDIOPATHIC MENTAL-RETARDATION | 0 | 0 |
| 1595 | 0 | 0 | 155 1983 MEDICINA-BUENOS AIRES 43(6):756-756 DELREY G; COCO R INVESTIGATION OF FRAGILE X-CHROMOSOMES IN MEN WITH MENTAL-RETARDATION (RM) OF UNKNOWN CAUSE | 0 | 0 |
| 1596 | 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 |
| 1597 | 0 | 0 | 159 1983 PATHOLOGY 15(1):105-106 JACKY PB; SUTHERLAND GR FRAGILE-X EXPRESSION IN FIBROBLASTS | 0 | 0 |
| 1598 | 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 |
| 1599 | 0 | 0 | 165 1983 TERATOLOGY 28(1):A30-A30 ISHIKIRIYAMA S; NIIKAWA N 2 JAPANESE PATIENTS WITH FRAGILE X SYNDROME | 0 | 2 |
| 1600 | 15 | 52 | 167 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(1):68-72 SCARBROUGH PR; COSPER P; FINLEY SC; SMITH NB FRAGILE-X SYNDROME - AN OVERVIEW | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1601 | 5 | 15 | 168 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(3):284-286 MIXON JC; DEV VG UNDERSTANDING THE FRAGILE X-SYNDROME | 0 | 2 |
| 1602 | 0 | 0 | 169 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(3):322-322 MIXON JC INHIBITION OF FRAGILE-X EXPRESSION BY 5-AZACYTIDINE (AZA) AND BY S-ADENOSYLHOMOCYSTEINE (SAH) | 0 | 0 |
| 1603 | 0 | 2 | 189 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(4):857-858 CHUDLEY AE; KNOLL JH; GERRARD JW FRAGILE-X MALES WITH NORMAL INTELLIGENCE - AND IF SO, WHY - REPLY | 0 | 0 |
| 1604 | 1 | 6 | 193 1984 CHINESE MEDICAL JOURNAL 97(11):861-864 XU BZ; REN S; XIAO GF; ZHOU XT A FRAGILE X SYNDROME FAMILY | 0 | 1 |
| 1605 | 0 | 0 | 198 1984 CLINICAL RESEARCH 32(5):A884-A884 FRIEDMAN JM; HOWARDPEEBLES PN A THEORETICAL-MODEL FOR UNAFFECTED CARRIER MALES IN FRAGILE-X FAMILIES | 0 | 0 |
| 1606 | 0 | 0 | 199 1984 CLINICAL RESEARCH 32(5):A885-A885 HOLMAN GH; ALLEN SM; TUCKER DA; TAWATER BA SEIZURES AND UNUSUAL VISUAL EVOKED-RESPONSES IN FRAGILE-X CARRIERS | 0 | 0 |
| 1607 | 0 | 0 | 200 1984 CYTOGENETICS AND CELL GENETICS 37(1-4):432-432 CAMERINO G; MATTEI MG; MATTEI JF; JAYE M; MANDEL JL CLOSE LINKAGE BETWEEN THE LOCI FOR THE FRAGILE X MENTAL-RETARDATION AND HEMOPHILIA-B | 0 | 0 |
| 1608 | 0 | 0 | 202 1984 EMERGENCY MEDICINE 16(15):103-& [Anon] IN SEARCH OF THE FRAGILE-X | 0 | 0 |
| 1609 | 0 | 0 | 209 1984 IRISH JOURNAL OF MEDICAL SCIENCE 153(1):29-30 DEARCE MA; LAW E A SIMPLE STATISTICAL APPROACH TO AVOID FALSE POSITIVES IN THE CYTOGENETIC DIAGNOSIS OF FRAGILE X-CHROMOSOMES | 0 | 0 |
| 1610 | 0 | 0 | 210 1984 JAPANESE JOURNAL OF GENETICS 59(6):618-619 HORI T; AYUSAWA D; SENO T EXPRESSION OF THE FRAGILE X-CHROMOSOME UNDER CONDITIONS OF THYMIDYLATE STRESS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1611 | 0 | 3 | 211 1984 JOURNAL DE GENETIQUE HUMAINE 32(3):193-197 CRIPPA L; DELOZIERBLANCHET CD; ENGEL E STUDIES OF THE CYTOGENETIC VARIATIONS OF THE FRAGILE-X (FRA-X) ACCORDING TO CASES AND METHODS | 0 | 3 |
| 1612 | 7 | 8 | 212 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 |
| 1613 | 0 | 1 | 215 1984 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 5(3):160-161 DESPOSITO F THE FRAGILE X-SYNDROME - DIAGNOSIS, BIOCHEMISTRY AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 1614 | 0 | 0 | 219 1984 JOURNAL OF MEDICAL GENETICS 21(4):298-298 WEBB TP; BUNDEY SE; THAKE A; TODD J STUDY OF THE FRAGILE X-CHROMOSOME AND MENTAL-RETARDATION | 0 | 3 |
| 1615 | 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 |
| 1616 | 0 | 0 | 231 1984 PATHOLOGY 16(1):108-108 SUTHERLAND GR THE FRAGILE X-CHROMOSOME | 0 | 0 |
| 1617 | 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 |
| 1618 | 1 | 26 | 240 1985 AMERICAN JOURNAL OF DANCE THERAPY 8:67-80 WOLFSCHEIN EG; FISCH GS; COHEN IL A STUDY OF THE USE OF NONVERBAL SYSTEMS IN THE DIFFERENTIAL-DIAGNOSIS OF AUTISTIC, MENTALLY-RETARDED AND FRAGILE X-INDIVIDUALS | 0 | 0 |
| 1619 | 0 | 1 | 253 1985 AMERICAN JOURNAL OF MENTAL DEFICIENCY 89(4):448-448 CROCKER AC THE FRAGILE X-SYNDROME - DIAGNOSIS, BIOCHEMISTRY, AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 1620 | 1 | 5 | 256 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):715-716 MILUNSKY A AN IMPORTANT CLINICAL APPROACH IN DETECTING THE FRAGILE X-SYNDROME | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1621 | 0 | 0 | 261 1985 CLINICAL CHEMISTRY 31(6):1008-1009 THIBODEAU SN; FAULK KR; SMITH AC; BERRY R; HAGERMAN R THE USE OF RECOMBINANT DNA TECHNIQUES TO DOCUMENT THE TRANSMISSION OF FRAGILE-X SYNDROME THROUGH AN UNAFFECTED MALE CARRIER | 0 | 0 |
| 1622 | 0 | 0 | 264 1985 CLINICAL GENETICS 27(3):307-307 FRYNS JP THE FRAGILE-X SYNDROME - A STUDY OF 83 INDEX-PATIENTS AND THEIR FAMILIES | 0 | 1 |
| 1623 | 0 | 0 | 271 1985 CLINICAL GENETICS 28(5):422-423 DAVIES KE; OLD J; MCGLADE S; SPEER A; COUTELLE C; et al. LINKAGE OF RFLPS AROUND THE DMD AND BMD LOCI AND THE FRAGILE X-LOCUS | 0 | 0 |
| 1624 | 0 | 0 | 272 1985 CLINICAL GENETICS 28(5):449-449 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; et al. FRAGILE X-SYNDROME AND MENTAL-RETARDATION IN GREECE | 0 | 0 |
| 1625 | 2 | 5 | 273 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):606-606 CONNOR JM; COLGAN JM; CROSSLEY JA; IMRIE SJ; YATES JRW; et al. MULTIPOINT LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE X-SYNDROME AND FAMILIES WITH HEMOPHILIA-B | 0 | 0 |
| 1626 | 1 | 5 | 274 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):612-612 DAVIES KE; HARPER K; MATTEI MG; MATTEI JF; VEENEMA H; et al. LINKAGE RELATIONSHIP OF DNA SEGMENT 52A (HGM7-DXS51) AND FACTOR-IX (HGM7-F9) TO FRAGILE-X MENTAL-RETARDATION (FRAXQ27) | 0 | 0 |
| 1627 | 0 | 0 | 275 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):645-645 GOONEWARDENA P; TOLUN A; GUSTAVSON KH; HOLMGREN G; LINDSTEN J; et al. STUDIES ON THE FRAGILE-X MENTAL-RETARDATION SYNDROME, DUCHENNE MUSCULAR-DYSTROPHY AND X-LINKED RETINITIS PIGMENTOSA IN SWEDISH FAMILIES, BY THE USE OF DNA PROBES | 0 | 0 |
| 1628 | 0 | 5 | 276 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):653-653 HOLDEN JJA; MULLIGAN LM; FORSTERGIBSON C; SIMPSON NE; WHITE BN; et al. APPLICATION OF FLANKING DNA PROBES TO CARRIER DETECTION IN THE FRAGILE-X SYNDROME | 0 | 2 |
| 1629 | 1 | 2 | 279 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):788-788 ZOLL B; ARNEMANN J; KRAWCZAK M; COOPER DN; PESCIA G; et al. THE LOCI FOR FRAGILE X-MENTAL RETARDATION SYNDROME AND COAGULATION FACTOR-IX ARE NOT CLOSELY LINKED | 0 | 0 |
| 1630 | 0 | 0 | 280 1985 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 27(1):95-96 PUESCHEL SM; FINELLI PV NEUROLOGICAL INVESTIGATIONS IN PATIENTS WITH FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1631 | 0 | 0 | 294 1985 JAPANESE JOURNAL OF HUMAN GENETICS 30(2):150-150 IKEDA T; MIYAGI C; HIRAYAMA K FRAGILE X-SYNDROME - REPORT OF 2 FAMILIES AND CYTOGENETIC STUDIES | 0 | 0 |
| 1632 | 0 | 3 | 298 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 LAWRENCE RJ THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME | 0 | 0 |
| 1633 | 1 | 6 | 304 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(2):239-240 HAGERMAN RJ; JACKSON AW AUTISM OR FRAGILE-X SYNDROME | 0 | 1 |
| 1634 | 1 | 1 | 305 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(2):240-240 SHELL J; CAMPBELL M AUTISM OR FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 1635 | 0 | 1 | 306 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(5):673-674 SZYMANSKI LS THE FRAGILE-X SYNDROME - DIAGNOSIS, BIOCHEMISTRY AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 1636 | 0 | 0 | 309 1985 NEUROPEDIATRICS 16(3):171-172 GRANSTROM ML; SIMOLA KOJ; YLINEN A; RINTAHAKA P THE FRAGILE-X SYNDROME IN CHILDHOOD - A THERAPEUTIC TRIAL WITH FOLIC-ACID | 0 | 0 |
| 1637 | 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 |
| 1638 | 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 |
| 1639 | 0 | 0 | 315 1986 ACTA NEUROLOGICA SCANDINAVICA 73(4):447-448 BAKKE JV FRAGILE-X SYNDROME AS A CONCOMITANT TO AND PROBABLE CAUSE OF MENTAL-RETARDATION | 0 | 0 |
| 1640 | 5 | 11 | 345 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):511-514 HOWARDPEEBLES PN METHIONINE METABOLISM AND FRAGILE-X EXPRESSION | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1641 | 0 | 0 | 358 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 25(1):186-187 DAR H; BAREL H; JAFFE M; WINTER ST THE FRAGILE-X SYNDROME - THE DILEMMA OF SELECTING PATIENTS FOR EXAMINATION | 0 | 1 |
| 1642 | 0 | 0 | 359 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 25(1):188-188 SHABTAI F; KLAR D; HART J; HALBRECHT I FRAGILE-X SYNDROME - A GENETIC OR AN INFECTIOUS-DISEASE | 0 | 0 |
| 1643 | 0 | 10 | 361 1986 ANNALES DE GENETIQUE 29(4):261-263 BELGHITI D; RAZAVIENCHA F; RAOUL O; HIRBEC G; GUILLOT F; et al. COINCIDENCE OF FAMILIAL SYSTEMIC LUPUS-ERYTHEMATOSUS AND THE FRAGILE-X SYNDROME | 0 | 3 |
| 1644 | 0 | 0 | 366 1986 ARCHIVOS DE BIOLOGIA Y MEDICINA EXPERIMENTALES 19(1):R133-R133 LACASSIE Y; MORENO R; ALLIENDE MA; DELABARRA F; BARAHONA G; et al. LACK OF EFFECT OF FOLIC-ACID THERAPY ON MENTAL RETARDED PATIENTS WITH FRAGILE-X OR OTHER AUTOSOMAL FRAGILITIES IN A DOUBLE-BLIND-STUDY | 0 | 0 |
| 1645 | 0 | 0 | 367 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(3):237-237 TURNER G; LAING S; ROBINSON H; PURVISSMITH S A PROGRAM FOR PRIMARY PREVENTION OF INTELLECTUAL HANDICAP - FRAGILE (X) SCREENING | 0 | 0 |
| 1646 | 0 | 0 | 368 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):350-350 LOESCH DZ; HAY D PHENOTYPIC DIVERSITY OF FRAGILE-X FEMALES AND ITS GENETIC-IMPLICATIONS | 0 | 0 |
| 1647 | 0 | 0 | 369 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):352-352 MULLEY JC; THORN K; SUTHERLAND GR LINKAGE RELATIONSHIPS OF THE FRAGILE-X | 0 | 0 |
| 1648 | 0 | 0 | 370 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):356-356 SUTHERLAND GR; BAKER E INDUCTION OF THE FRAGILE-X IN FIBROBLASTS BY THYMIDINE | 0 | 0 |
| 1649 | 0 | 0 | 371 1986 BIOPHYSICAL JOURNAL 49(2):A18-A18 STUTZIN A; POLLARD HB SYNEXIN-INDUCED FUSION OF CHROMAFFIN GRANULE GHOSTS (CGG) STUDIED BY A NOVEL FLUORESCENCE ASSAY | 0 | 0 |
| 1650 | 2 | 6 | 373 1986 BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE 102(12):1742-1745 ZAKHAROV AF; BEDELBAEVA KA; BARANOVSKAYA LI VARIABILITY OF FRAGILE X-CHROMOSOME EXPRESSION IN CONSECUTIVE CELL GENERATIONS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1651 | 16 | 37 | 374 1986 CHILD STUDY JOURNAL 16(4):285-296 BURD L; KERBESHIAN J FRAGILE X-SYNDROME - DEVELOPMENTAL ASPECTS | 0 | 1 |
| 1652 | 0 | 0 | 375 1986 CLINICAL CHEMISTRY 32(6):1215-1215 THIBODEAU SN THE USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS (RFLP) TO DETERMINE THE CARRIER STATUS OF FRAGILE-X-SYNDROME | 0 | 0 |
| 1653 | 3 | 5 | 377 1986 CLINICAL GENETICS 29(2):95-95 DEARCE MA; HECHT F; SUTHERLAND GR; WEBB GC GUIDELINES FOR THE DIAGNOSIS OF FRAGILE X | 0 | 2 |
| 1654 | 0 | 0 | 383 1986 CLINICAL RESEARCH 34(1):A34-A34 VANDYKE DL; WEISS L MATERNAL EFFECT ON INTELLIGENCE IN FRAGILE-X MALES AND FEMALES - AN HYPOTHESIS | 0 | 0 |
| 1655 | 0 | 0 | 384 1986 CLINICAL RESEARCH 34(1):A114-A114 LOEHR JP; SYNHORST DP; HAGERMAN RJ; WOLFE RR CARDIOVASCULAR-ABNORMALITIES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1656 | 0 | 1 | 388 1986 FEDERATION PROCEEDINGS 45(3):702-702 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE X EXPRESSION IN THE PRESENCE OF 5-FLUORO-2'-DEOXYURIDINE (FUDR) | 0 | 0 |
| 1657 | 0 | 0 | 392 1986 JAPANESE JOURNAL OF HUMAN GENETICS 31(2):150-150 ARINAMI T; TAKANAWA S; KONDO I THE FRAGILE X-SYNDROME IN A JAPANESE POPULATION OF INSTITUTIONALIZED MENTALLY-RETARDED MALES | 0 | 0 |
| 1658 | 0 | 0 | 393 1986 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 7(3):201-202 LACHIEWICZ AM; GULLION CM; SPIRIDIGLIOZZI GA; ALYSWORTH AS DECLINE IN IQ SCORES OF YOUNG FRAGILE X-MALES | 0 | 0 |
| 1659 | 0 | 0 | 395 1986 JOURNAL OF MEDICAL GENETICS 23(2):166-166 WEBB TP; BUNDEY SE; THAKE A; TODD J THE PREVALENCE OF THE FRAGILE-X SYNDROME IN SCHOOLCHILDREN IN COVENTRY | 0 | 0 |
| 1660 | 14 | 52 | 402 1986 JOURNAL OF PEDIATRIC PSYCHOLOGY 11(1):91-102 MADISON LS; MOSHER GA; GEORGE CH FRAGILE-X SYNDROME - DIAGNOSIS AND RESEARCH | 0 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1661 | 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 |
| 1662 | 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 |
| 1663 | 5 | 13 | 419 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):987-990 MULLEY JC; SUTHERLAND GR FRAGILE-X TRANSMISSION AND THE DETERMINATION OF CARRIER PROBABILITIES FOR GENETIC-COUNSELING | 0 | 11 |
| 1664 | 0 | 0 | 429 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):75-75 LOESCH DZ DERMATOGLYPHIC ABNORMALITY IN FRAGILE X-SYNDROME - A NEW CAUSAL HYPOTHESIS | 0 | 0 |
| 1665 | 0 | 0 | 430 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 |
| 1666 | 0 | 0 | 431 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):81-81 SUTHERLAND GR; BAKER E; HOCKEY A; PURVISSMITH S THE USE OF THYMIDINE INDUCTION OF THE FRAGILE X-CHROMOSOME IN PRENATAL-DIAGNOSIS | 0 | 0 |
| 1667 | 0 | 0 | 432 1987 BEHAVIOR GENETICS 17(6):642-642 VANDENBERG SG A STATUS-REPORT ON THE FRAGILE X-SYNDROME | 0 | 0 |
| 1668 | 0 | 0 | 439 1987 CLINICAL RESEARCH 35(1):A60-A60 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE-X (FRA-X) EXPRESSION IN THE PRESENCE OF 5-FLOURO-2'-DEOXYURIDINE (FDUMP) | 0 | 0 |
| 1669 | 0 | 0 | 440 1987 CLINICAL RESEARCH 35(1):A60-A60 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| 1670 | 0 | 0 | 441 1987 CLINICAL RESEARCH 35(1):A211-A211 HAGERMAN RJ; JACKSON AW; BERRY R; CAMPBELL J; STILLMAN E; et al. PREDICTORS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1671 | 1 | 22 | 442 1987 COLLEGIUM ANTROPOLOGICUM 11(2):305-316 LOESCH DZ FACTOR-ANALYSIS OF RIDGE-PATTERNS AND HAND MEASUREMENTS IN NORMAL AND FRAGILE-X MALES | 0 | 2 |
| 1672 | 0 | 0 | 445 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):594-594 CLAYTON JF; GOSDEN CM; HASTIE N; EVANS HJ MULTIPOINT ANALYSIS AND FRAGILE-X | 0 | 0 |
| 1673 | 0 | 0 | 446 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):598-598 CONNOR JM; OSMAN H; STEFANI L; NEVIN NC; HOFKER M LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE-X SYNDROME USING CX55-7 (DXS105) | 0 | 2 |
| 1674 | 0 | 0 | 447 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):622-622 GOSDEN C; BUCHANAN J; NEWTON M; KESTON M; WRIGHT AF; et al. FRAGILE-X SYNDROME - NEW LINKAGE DATA IN 10 FAMILIES | 0 | 0 |
| 1675 | 0 | 0 | 449 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):690-690 SENIOR J; KILPATRICK M; WEBB T LINKAGE STUDIES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1676 | 1 | 2 | 453 1987 HASTINGS CENTER REPORT 17(1):2-3 [Anon] TO SCREEN OR NOT TO SCREEN FOR THE FRAGILE X-SYNDROME | 0 | 0 |
| 1677 | 0 | 0 | 465 1987 INTERNATIONAL JOURNAL OF NEUROSCIENCE 34(3-4):172-172 FERRI R; BERGONZI P; COLOGNOLA RM; MUSUMECI SA; PETRELLA MA; et al. BRAIN-STEM AUDITORY AND VISUAL EVOKED-POTENTIALS IN FRAGILE-X MENTAL-RETARDATION SYNDROME SUBJECTS | 0 | 0 |
| 1678 | 0 | 0 | 466 1987 JAPANESE JOURNAL OF GENETICS 62(6):520-520 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M STRUCTURAL ALTERATION IN FRA(X)(Q27.3) ASSOCIATED WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1679 | 0 | 0 | 467 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):122-123 SUGIO Y FRAGILE-X SYNDROME - COLLABORATIVE STUDIES OF JAPANESE PATIENTS | 0 | 0 |
| 1680 | 0 | 0 | 468 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):170-171 ARINAMI T; NAKAJIMA S; KONDO I THE FRAGILE X-SYNDROME IN A JAPANESE POPULATION OF INSTITUTIONALIZED MENTALLY-RETARDED FEMALES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1681 | 0 | 0 | 469 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):171-171 KASAI R; NARAHARA K; MURAKAMI M; KIKKAWA K; KIMURA S; et al. PREVALENCE OF THE FRAGILE(X) SYNDROME IN INSTITUTIONALIZED MENTALLY-RETARDED INDIVIDUALS | 0 | 0 |
| 1682 | 0 | 0 | 470 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):210-211 ARINAMI T; TAMURA K; KONDO I A FRAGILE X-FEMALE WITH DOWN-SYNDROME - A CASE-REPORT | 0 | 0 |
| 1683 | 0 | 0 | 475 1987 JOURNAL OF MEDICAL GENETICS 24(4):240-240 WINTER RM POPULATION-GENETICS IMPLICATIONS OF THE PREMUTATION HYPOTHESIS FOR THE GENERATION OF THE FRAGILE-X MENTAL-RETARDATION GENE | 0 | 0 |
| 1684 | 4 | 5 | 485 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(6):938-938 HAGERMAN RJ FRAGILE-X CHROMOSOME AND LEARNING-DISABILITY | 0 | 0 |
| 1685 | 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 |
| 1686 | 0 | 0 | 504 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-20 KAHKONEN M; ALITALO T; AIRAKSINEN E; MATILAINER R; LAUNIALA K; et al. PREVALENCE OF THE FRAGILE-X OR MARTIN-BELL SYNDROME | 0 | 0 |
| 1687 | 0 | 0 | 506 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):21-21 LEDBETTER DH; LEDBETTER SA HIGH-LEVELS OF FRAGILE-X EXPRESSION IN NORMAL MALES INDUCED BY APHIDICOLIN | 0 | 0 |
| 1688 | 0 | 0 | 507 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):22-22 LEISTI J; KAHKONEN M; HERVA R; WINQVIST R; UKKOLA L; et al. THE FRAGILE-X SYNDROME IN NORTHERN FINLAND - A GENEALOGIC STUDY | 0 | 0 |
| 1689 | 0 | 0 | 508 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):22-23 OBERLE I; ARVEILER B; WOELFLIN A; HOFKER M; PEARSON P; et al. GENETIC AND PHYSICAL MAPPING OF THE FRAGILE-X REGION - .A. NEW POLYMORPHIC MARKERS .B. IS THE FRAGILE-X SITE A PREFERENTIAL BREAKPOINT IN CHROMOSOME REARRANGEMENTS | 0 | 0 |
| 1690 | 0 | 0 | 509 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):23-24 RUDELLI R; MADRID R; BROWN WT FURTHER NEUROPATHOLOGICAL OBSERVATIONS IN ADULT FRAGILE-X | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1691 | 0 | 0 | 510 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):25-25 TOMMERUP N; REINTOFT I; RESKENIELSEN E; BRONDUMNIELSEN K; MIKKELSEN M UNSUSPECTED PRENATAL-DIAGNOSIS OF THE FRAGILE-X | 0 | 1 |
| 1692 | 0 | 0 | 511 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):26-26 TOMMERUP N; TRANEBJAERG L; TONNESEN T; KASTERN W; HANSEN H; et al. IDENTICAL EXPRESSION OF THE FRAGILE-X BUT DISCORDANT CLINICAL MANIFESTATIONS IN MONOZYGOTIC TWINS WITH MARTIN-BELL SYNDROME | 0 | 0 |
| 1693 | 0 | 0 | 512 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):26-27 TURNER G; PARTINGTON MW; ROBINSON H; LATHAM M; KENNY J; et al. THE PROS AND CONS OF PREVENTIVE SCREENING FOR THE FRAGILE (X) | 0 | 0 |
| 1694 | 196 | 429 | 513 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):31-60 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X AND RELATED SUBJECTS-IV (1988) | 0 | 1 |
| 1695 | 11 | 14 | 529 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):337-345 PURVISSMITH SG; LAING S; SUTHERLAND GR; BAKER E PRENATAL-DIAGNOSIS OF THE FRAGILE-X - THE AUSTRALASIAN EXPERIENCE | 0 | 14 |
| 1696 | 3 | 4 | 532 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):369-376 SANFILIPPO S; RAGUSA RM; SCILLATO F; RUGGERI M; NERI G FRAGILE-X EXPRESSION IN NORMAL AND MENTALLY-RETARDED SUBJECTS - EFFECT OF TREATMENT WITH AN ANTIFOLIC AGENT | 0 | 4 |
| 1697 | 1 | 3 | 540 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):455-457 HOWARDPEEBLES P; FROSTERISKENIUS U FRAGILE-X TESTING IN MOTHERS OF TRANSMITTING MALES | 0 | 1 |
| 1698 | 5 | 12 | 561 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):775-778 BUTLER MG; DEV VG; SHAH D; ULM JE; WILMOT PL; et al. THE USE OF EARLY SIMULTANEOUS PERCUTANEOUS UMBILICAL BLOOD-SAMPLING (PUBS) AND AMNIOCENTESIS FOR PRENATAL FRAGILE-X CHROMOSOME DIAGNOSIS | 0 | 0 |
| 1699 | 0 | 0 | 565 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):91-91 TURNER G ISSUES ARISING FROM FRAGILE-X PREVENTIVE SCREENING | 0 | 0 |
| 1700 | 0 | 0 | 566 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):91-91 LAING S; LATHAM M; KENNY J; PURVISSMITH S; TURNER G CYTOGENETIC ANOMALIES IN A POPULATION SELECTED FOR FRAGILE-X SCREENING | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1701 | 0 | 0 | 567 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):93-94 GARRY MB; MACFARLANE SC; PULLON DHH FRAGILE-X POSITIVE TURNERS MOSAIC | 0 | 0 |
| 1702 | 0 | 0 | 568 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):96-96 PURVISSMITH S; LAING S; STEWART L; TURNER G; WASS D; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X | 0 | 0 |
| 1703 | 0 | 2 | 569 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):97-97 SUTHERS GK; THODE A; TURNER GL CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS | 0 | 0 |
| 1704 | 2 | 19 | 572 1988 CHROMOSOMA 96(5):391-396 SAVAGE JRK; FITCHETT M THE BEHAVIOR OF FRAGILE-X AND OTHER ABERRATIONS DURING RECOVERY FROM LOW FOLATE CONDITIONS | 0 | 3 |
| 1705 | 6 | 13 | 574 1988 CLINICAL GENETICS 33(3):169-175 LOESCH DZ DISCRIMINANT-ANALYSIS OF DERMATOGLYPHIC MEASUREMENTS IN FRAGILE-X MALES AND FEMALES | 0 | 1 |
| 1706 | 0 | 0 | 577 1988 CLINICAL GENETICS 33(6):464-464 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 0 | 0 |
| 1707 | 0 | 0 | 579 1988 CLINICAL RESEARCH 36(1):A207-A207 BIXENMAN H; HECHT F; LOCKWOOD D; HECHT BK NEW COMMON FRAGILE SITE AT XQ27.3 CONFOUNDED WITH FRAGILE-X | 0 | 0 |
| 1708 | 6 | 24 | 581 1988 CYTOGENETICS AND CELL GENETICS 48(3):142-147 FANTES J; GOSDEN J; PIPER J USE OF AN ALPHOID SATELLITE SEQUENCE TO LOCATE THE X-CHROMOSOME AUTOMATICALLY, WITH PARTICULAR REFERENCE TO IDENTIFICATION OF THE FRAGILE-X | 0 | 4 |
| 1709 | 2 | 13 | 583 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(5):646-649 CAMMARATA S; ARCHIDIACONO N; ROMEO G; BENASSI G; GUARINO M; et al. PREVALENCE OF MENTAL-RETARDATION RELATED TO FRAGILE X SYNDROME AND OTHER CHROMOSOMAL-ABNORMALITIES IN THE REPUBLIC OF SAN MARINO | 0 | 2 |
| 1710 | 1 | 2 | 585 1988 HUMAN GENETICS 78(2):196-197 SUBRT I; STIRSKA K FREQUENCY OF TRIRADIAL AND MULTIRADIAL CONFIGURATIONS IN FRAGILE X-CHROMOSOMES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1711 | 0 | 0 | 595 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):224-224 ARINAMI T; SATO M; KONDO I AUDITORY BRAIN-STEM RESPONSES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1712 | 0 | 0 | 596 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):225-225 KONDO I; ARINAMI T PREVALENCE OF CHROMOSOME-ANOMALIES IN MENTALLY-RETARDED SCHOOL-CHILDREN - STUDY OF POPULATION INCIDENCE OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1713 | 0 | 0 | 597 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):245-245 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M EXPRESSION OF FRA(X)(Q27.3) ASSOCIATED WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1714 | 0 | 1 | 600 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):457-458 WOLFSCHEIN EG; JENKINS EC; SKLOWER S; COHEN IL; WISNIEWSKI KE; et al. ON THE ASSOCIATION OF FRAGILE-X WITH AUTISM | 0 | 0 |
| 1715 | 0 | 0 | 601 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):458-458 SCHOPLER E ON THE ASSOCIATION OF FRAGILE-X WITH AUTISM - RESPONSE | 0 | 0 |
| 1716 | 1 | 1 | 605 1988 JOURNAL OF MEDICAL GENETICS 25(1):64-64 LACA Z; BRANKOVIC S EXPRESSION OF FRAGILE X-CHROMOSOME AND POSSIBLE DELETION IN SUCCESSIVE CELL DIVISIONS | 0 | 0 |
| 1717 | 0 | 0 | 606 1988 JOURNAL OF MEDICAL GENETICS 25(2):128-128 ENGLISH C ANTHROPOMETRIC STUDIES IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 1718 | 0 | 0 | 607 1988 JOURNAL OF MEDICAL GENETICS 25(2):129-129 DAVIES KE; PATTERSON M; BELL M; KENWRICK SJ MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 1719 | 0 | 0 | 608 1988 JOURNAL OF MEDICAL GENETICS 25(2):131-131 MCKINLEY MJ; KEARNEY LU; NICOLAIDES K PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY PLACENTAL BIOPSY | 0 | 0 |
| 1720 | 0 | 0 | 610 1988 NEUROTOXICOLOGY 9(1):139-140 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1721 | 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 |
| 1722 | 2 | 7 | 619 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):978-979 ARINAMI T BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 1723 | 7 | 18 | 620 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 |
| 1724 | 0 | 0 | 626 1989 AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 78(2):200-200 BUTLER MG; HAYNES JL; ALLEN GA; SINGH DN ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT FRAGILE X-SYNDROME | 0 | 0 |
| 1725 | 2 | 17 | 631 1989 ARCHIVES OF NEUROLOGY 46(12):1269-1270 GRIGSBY J; HAGERMAN R FRAGILE-X SYNDROME - A GENETIC ETIOLOGY FOR DEVELOPMENTAL GERSTMANN SYNDROME | 0 | 0 |
| 1726 | 0 | 29 | 632 1989 BLOOD 74(2):828-832 MORLE L; MORLE F; ROUX AF; GODET J; FORGET BG; et al. SPECTRIN TUNIS (SP-ALPHA-I/78), AN ELLIPTOCYTOGENIC VARIANT, IS DUE TO THE CGG -] TGG CODON CHANGE (ARG -] TRP) AT POSITION-35 OF THE ALPHA-I DOMAIN | 0 | 33 |
| 1727 | 0 | 0 | 636 1989 CLINICAL RESEARCH 37(1):A170-A170 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; et al. LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 0 | 0 |
| 1728 | 0 | 0 | 638 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):982-982 DAHL N; MALMSTROM H; HAMMARSTROMHEEROMA K; WADELIUS C; GUSTAVSON KH; et al. ISOLATION OF A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) | 0 | 3 |
| 1729 | 0 | 0 | 639 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1007-1007 GOONEWARDENA P; GROSS AC; FERRANDO CJ; BROWN T; DAHL N; et al. ANONYMOUS DNA PROBE U6.2 (DXS304) FROM XQ MAPS DISTAL TO THE DXS98 LOCUS AND SHOWS CLOSE LINKAGE TO THE FRAGILE-X SYNDROME | 0 | 1 |
| 1730 | 0 | 0 | 640 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1009-1009 GROSS AC; FERRANDO CJ; BROWN WT LINKAGE DATA FOR FRAGILE-X AND 3 DISTAL MARKERS | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1731 | 0 | 0 | 642 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1089-1090 THIBODEAU SN; SCHAID D; BREN G; BLOOMFIELD J; BELL MV; et al. GENETIC-MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 0 | 1 |
| 1732 | 0 | 1 | 643 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1100-1101 WAHLSTROM J; WITTENGERSTROM I; ANVRET M; ODEN A; JOHANNESSON T; et al. RETT SYNDROME RELATED TO FRAGILE X(P22) IN CAFFEINE-INDUCED LYMPHOCYTES CULTURES | 0 | 2 |
| 1733 | 0 | 1 | 651 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(4):643-643 LACHIEWICZ AM FRAGILE-X SYNDROME - A HANDBOOK FOR FAMILIES AND EDUCATORS - FINUCANE,B | 0 | 0 |
| 1734 | 1 | 5 | 659 1989 LANCET 2(8657):279-279 SCHEPIS C; PALAZZO R; RAGUSA RM; SPINA E; BARLETTA C ASSOCIATION OF CUTIS VERTICIS GYRATA WITH FRAGILE-X SYNDROME AND FRAGILITY OF CHROMOSOME-12 | 0 | 11 |
| 1735 | 0 | 1 | 661 1989 NATURE 341(6243):580-580 HARRIS A; BOBROW M THE FRAGILE-X SYNDROME - DAVIES,KE | 0 | 0 |
| 1736 | 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 |
| 1737 | 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 |
| 1738 | 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 |
| 1739 | 1 | 2 | 687 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):433-433 MEISNER LF FRAGILE-X FREQUENCY | 0 | 0 |
| 1740 | 1 | 1 | 688 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):434-434 MINGRONINETTO RC; ROSENBERG C; VIANNAMORGANTE AM; PAVANELLO RCM FRAGILE-X FREQUENCY - RESPONSE | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1741 | 2 | 6 | 689 1990 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 163(5):1713-1714 SINDWANI V; VERMA RS CYTOGENETIC UNCERTAINTIES SURROUNDING THE FRAGILE X IN MARTIN-BELL SYNDROME | 0 | 0 |
| 1742 | 8 | 13 | 692 1990 ANNALES DE GENETIQUE 33(2):109-110 LUCOTTE G A NEW DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1743 | 0 | 0 | 693 1990 ANNALS OF NEUROLOGY 28(3):440-440 BERRYKRAVIS E; HUTTENLOCHER PR CYCLIC-AMP METABOLISM IN FRAGILE X-SYNDROME | 0 | 0 |
| 1744 | 1 | 40 | 694 1990 ARCHIVES FRANCAISES DE PEDIATRIE 47(10):701-703 PIUSSAN C X-LINKED MENTAL-RETARDATION WITHOUT FRAGILE X-CHROMOSOME | 0 | 0 |
| 1745 | 1 | 14 | 697 1990 BRAIN & DEVELOPMENT 12(1):128-130 WAHLSTROM J; WITTENGERSTROM I; MELLQUIST L; ANVRET M; ODEN A THE RETT SYNDROME RELATED TO FRAGILE-X(P22) IN CAFFEINE-INDUCED LYMPHOCYTE CULTURE | 0 | 13 |
| 1746 | 2 | 14 | 698 1990 BRITISH DENTAL JOURNAL 168(4):160-162 NUNN JH; DURNING P FRAGILE-X (MARTIN BELL) SYNDROME AND DENTAL-CARE | 0 | 0 |
| 1747 | 0 | 0 | 703 1990 CLINICAL RESEARCH 38(1):A164-A164 HAGERMAN R; AMIRI K; CRONISTER A; WITTENBERGER M; SCHREINER R; et al. FRAGILE-X GIRLS - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 0 | 0 |
| 1748 | 1 | 12 | 704 1990 CYTOMETRY 11(1):73-79 PIPER J; FANTES J; GOSDEN J; JI L AUTOMATIC DETECTION OF FRAGILE X-CHROMOSOMES USING AN X-CENTROMERE PROBE | 0 | 4 |
| 1749 | 10 | 27 | 705 1990 EUROPEAN NEUROLOGY 30(1):32-37 RAIMONDI E; LENTI C; ROMAGNONI M; NEGRI R; GAMBINI E; et al. FRAGILE-X MENTAL-RETARDATION IN A LARGE 5-GENERATION FAMILY - A CLINICAL AND CYTOGENETIC STUDY | 0 | 0 |
| 1750 | 5 | 7 | 709 1990 HUMAN GENETICS 85(1):141-142 SUTHERS GK; SUTHERLAND GR RECOMBINATION AND THE FRAGILE-X | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1751 | 18 | 36 | 713 1990 JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME 72A(6):889-896 DAVIDS JR; HAGERMAN RJ; EILERT RE ORTHOPEDIC ASPECTS OF FRAGILE-X SYNDROME | 0 | 13 |
| 1752 | 0 | 1 | 714 1990 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 31(7):1165-1166 BOLTON P THE FRAGILE X-SYNDROME - DAVIES,K | 0 | 0 |
| 1753 | 0 | 0 | 716 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 |
| 1754 | 0 | 0 | 717 1990 JOURNAL OF MEDICAL GENETICS 27(3):208-209 WEBB T PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1755 | 3 | 7 | 719 1990 JOURNAL OF MENTAL DEFICIENCY RESEARCH 34:81-86 COLLACOTT RA; DUCKETT DP; MATHEWS D; WARRINGTON JS; YOUNG ID DOWNS-SYNDROME AND FRAGILE-X SYNDROME IN A SINGLE PATIENT | 0 | 0 |
| 1756 | 5 | 11 | 723 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(1):1-2 GOODYEAR HM; SONKSON PM FRAGILE X-SYNDROME - AN IMPORTANT CAUSE OF MENTAL-RETARDATION | 0 | 0 |
| 1757 | 0 | 1 | 724 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(6):415-415 HALSTEAD S FRAGILE X-SYNDROME | 0 | 0 |
| 1758 | 0 | 0 | 725 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(6):415-415 GOODYEAR HM; SONKSON PM FRAGILE X-SYNDROME - REPLY | 0 | 0 |
| 1759 | 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 |
| 1760 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1761 | 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 |
| 1762 | 0 | 0 | 735 1990 PRACTITIONER 234(1496):946-& BERNEY T FRAGILE-X SYNDROME | 0 | 0 |
| 1763 | 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 |
| 1764 | 0 | 1 | 743 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(4):815-815 FINUCANE B; SCOTT CI; KURTZ MB CONCURRENCE OF DOMINANT PIEBALD TRAIT AND FRAGILE X-SYNDROME | 0 | 2 |
| 1765 | 0 | 0 | 747 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):35-35 TURNER G FRAGILE X-SYNDROME | 0 | 0 |
| 1766 | 0 | 1 | 748 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 SCHLESSINGER D; ZUCCHI I; NAGARAJA R; LITTLE RD; ABIDI F; et al. CLONING OF THE FRAGILE-X LOCUS IN THE CONTEXT OF YEAST ARTIFICIAL CHROMOSOME-BASED MAPPING OF XQ24-28 | 0 | 0 |
| 1767 | 0 | 0 | 749 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 POUSTKA A; DIETRICH A; KORN B; GROSS B; MONACO A; et al. MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION | 0 | 0 |
| 1768 | 0 | 0 | 750 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 KUHL D; PIERETTI M; REINER O; NELSON D FRAGILE-X SITE - MOLECULAR AND GENETIC-CHARACTERIZATION | 0 | 0 |
| 1769 | 0 | 0 | 751 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):76-76 OBERLE I; ROUSSEAU F; HEITZ D; DEVYS D; ZENGERLING S; et al. MOLECULAR-BASIS OF THE FRAGILE-X SYNDROME AND DIAGNOSTIC APPLICATIONS | 0 | 0 |
| 1770 | 0 | 0 | 752 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):76-76 YU S; KREMER E; PRITCHARD M; LYNCH M; NANCARROW J; et al. THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1771 | 0 | 0 | 753 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):103-103 ROCCHI M; MORABITO E; DINATALE P IDURONATE SULFATASE ACTIVITY ON LYMPHOBLASTOID CELL-LINES FROM SUBJECTS AFFECTED BY FRAGILE-X SYNDROME | 0 | 0 |
| 1772 | 0 | 0 | 754 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):139-139 HAGERMAN RJ; BRUNSCHWIG A; MILLER L; BUTLER MG SELECTED STANDARDS FOR ANTHROPOMETRIC MEASUREMENTS IN FRAGILE X-SYNDROME | 0 | 0 |
| 1773 | 0 | 0 | 755 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):158-158 RAMZY MI; SALINAS CF ORODENTAL FINDINGS IN AN EGYPTIAN SAMPLE OF FRAGILE-X CASES | 0 | 0 |
| 1774 | 0 | 0 | 756 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):159-159 REISS A; FREUND L; AYLWARD E NEUROANATOMY OF THE FRAGILE X SYNDROME | 0 | 0 |
| 1775 | 0 | 0 | 757 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):163-163 SEEMANOVA E; GOETZ P; SVOBODOVA M; LESNY I INCESTUOUS MATINGS IN FAMILIES WITH FRAGILE (X) SYNDROME | 0 | 0 |
| 1776 | 0 | 0 | 758 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):194-194 KUHL DPA; WARREN ST; RIGGINS GJ; NELSON DL; CASKEY CT USE OF CA REPEAT MARKER DXS548 FOR PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME AND THE IDENTIFICATION OF NEW POSSIBLY POLYMORPHIC SITES IN THE FRAGILE-X REGION | 0 | 0 |
| 1777 | 0 | 0 | 759 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):211-211 BROWN WT; GOONEWARDENA P; RAY J; MIEZEJESKI C; KRAWCZUN M; et al. PRENATALLY DETECTED FRAGILE X FEMALES - COUNSELING ISSUES AND LONG-TERM FOLLOW-UPS | 0 | 0 |
| 1778 | 0 | 0 | 760 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):221-221 KAHKONEN M; VAISANEN ML; WINGVIST R; LEISTI J PRENATAL-DIAGNOSIS OF FRAGILE X SYNDROME | 0 | 0 |
| 1779 | 0 | 0 | 762 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):235-235 LI Q; XU DD; ZHOU LY FRAGILE X-FREQUENCY IN MENTALLY-RETARDED CHILDREN AND IN FETAL BLOOD BY CORDOCENTESIS | 0 | 0 |
| 1780 | 0 | 0 | 763 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):257-257 JACKSONCOOK J; PISERCHIO C; VIRGINIA J MOSAIC XY/XYY AND FRAGILE-X IN A 4-YEAR-OLD MALE BODURTHA | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1781 | 0 | 0 | 764 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):267-267 KARIMINEJAD MH; RAHIMI M; SHIRNESHAN K; VAEZI SA; KARIMINEJAD R FRAGILE-X (BELL,MARTIN) SYNDROME IN AN IRANIAN FAMILY WITH 8 AFFECTED MEMBERS | 0 | 0 |
| 1782 | 0 | 0 | 765 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):269-269 LOZZIO CB; MATTESON K; CACHEIRO NL CARRIER DETECTION OF FRAGILE-X USING TRIMETHOPRIM AND DNA LINKAGE ANALYSES | 0 | 0 |
| 1783 | 0 | 0 | 766 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):269-269 PAJARES IL; DELICADO A; DETORRES ML; MARTIN VL; CASTROVIEJO IP; et al. FRAGILE-X SYNDROME WITH EXTRAMICROCHROMOSOME | 0 | 0 |
| 1784 | 0 | 1 | 767 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):270-270 MURTHY SK; KAR B FRAGILE-X SYNDROME IN MENTALLY-RETARDED POPULATION OF WESTERN INDIA | 0 | 0 |
| 1785 | 0 | 0 | 768 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):273-273 RISCILE GR FRAGILE-X PATIENTS WITH ATYPICAL PHENOTYPES | 0 | 0 |
| 1786 | 0 | 0 | 769 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):280-280 ZASLAV AL; BROWN WT THE SIGNIFICANCE OF LOW-LEVEL FRAGILE X EXPRESSION | 0 | 0 |
| 1787 | 0 | 0 | 770 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):287-287 RAFI SK; SURANA RB; ANDERSON LH; CHRISTOPHER KL; WILSON B; et al. HYPEROXIA ENHANCES THE INDUCTION OF FRAGILE-X SITE OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1788 | 0 | 0 | 771 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):289-289 BUCKLEY D; JALAL S; DEWALD G FRAGILE-X STUDIES - WHAT IS PRACTICAL | 0 | 0 |
| 1789 | 0 | 0 | 772 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):290-290 JENKINS E; GENOVESE M; DUNCAN C; GU H; SCHWARTZRICHSTEIN C; et al. COMMON FRAGILE SITE FRA(X)(Q27.2), PRESENT IN ONLY 1 OF 685 CASES SCREENED FOR THE FRAGILE-X SYNDROME | 0 | 0 |
| 1790 | 0 | 0 | 773 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):290-290 HOWARDPEEBLES PN FRAGILE-X TESTING OF FAMILY MEMBERS IN THE CLINICAL CYTOGENETICS LABORATORY - PERIMETERS AND PITFALLS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1791 | 0 | 0 | 774 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):291-291 LOGHINGROSSO NS; LAUANDOS JE; ALI VRA; GRACA CHN; SCHMIDT BJ SEARCHING FOR FRAGILE-X IN AN INSTITUTION FOR MENTALLY-HANDICAPPED IN BRAZIL | 0 | 0 |
| 1792 | 0 | 0 | 775 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):292-292 SHAPIRO LR; PETRELLA R; EALLONARDO SJ; WILMOT PL RELIABILITY OF OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION AS AN INDICATION OF SUCCESSFUL INDUCTION OF THE FRAGILE-X CHROMOSOME | 0 | 0 |
| 1793 | 0 | 0 | 776 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):293-293 TENGSTROM C; AUTIO S CHROMOSOMAL-ABERRATIONS IN 542 MENTALLY-RETARDED PATIENTS EXAMINED BY HIGH-RESOLUTION BANDING INCLUDING FRAGILE X-SCREENING | 0 | 0 |
| 1794 | 0 | 0 | 777 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):303-303 MCCOMBS J; ROUSE B; LOCKHART L; HOWARDPEEBLES P PRENATAL IDENTIFICATION OF FRAGILE-X AND A MARKER CHROMOSOME | 0 | 0 |
| 1795 | 0 | 0 | 778 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):331-331 TURNER G; ROBINSON H; LAING S; SHERMAN S SCREENING FOR THE FRAGILE X-SYNDROME - IMPACT OF GENETIC-COUNSELING ON REPRODUCTIVE CHOICES OF WOMEN AT RISK FOR HAVING AN AFFECTED CHILD | 0 | 0 |
| 1796 | 0 | 0 | 779 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):338-338 GLASS IA; DELMASTRO RG; LANYON WG; RAEBURN JA; KILPATRICK MW; et al. IDENTIFICATION OF DIAGNOSTIC DNA MARKERS FOR THE FRAGILE-X SYNDROME | 0 | 0 |
| 1797 | 0 | 0 | 780 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):341-341 GOONEWARDENA P; GLICKSMAN A; BROWN WT LINKAGE ANALYSIS OF PROXIMAL DNA MARKERS RN1 AND VK23 USED IN THE DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| 1798 | 0 | 0 | 781 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):353-353 NORDSTROM AM; VONKOSKULL H LINKAGE TO DXS52 IN A FRAGILE-X NEGATIVE FAMILY | 0 | 0 |
| 1799 | 0 | 0 | 782 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):357-357 RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; et al. A FREQUENT DINUCLEOTIDE POLYMORPHISM OF THE FRAGILE-X BREAKPOINT CLUSTER REGION IS TIGHTLY LINKED TO THE FRAGILE-X SYNDROME LOCUS | 0 | 0 |
| 1800 | 0 | 0 | 783 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):383-383 LEE JT; MURGIA A; WARREN S; NELSON D; NUSSBAUM R CONSTRUCTION OF A 600-KB YAC CONTIG PROXIMAL TO THE FRAGILE X-SITE | 0 | 0 |