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Journal Abstract Search

345 related items for PubMed ID: 2895523

  • 1. Genetics and expression of the fragile X syndrome.
    Brown WT, Jenkins EC, Gross AC, Chan CB, Wisniewski K, Cohen IL, Miezejeski CM.
    Ups J Med Sci Suppl; 1987; 44():137-54. PubMed ID: 2895523
    [Abstract] [Full Text] [Related]

  • 2. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P, Dahl N, Gustavson KH, Holmgren G, Pettersson U.
    Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524
    [Abstract] [Full Text] [Related]

  • 3. The fragile X syndrome.
    Brown WT.
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
    [Abstract] [Full Text] [Related]

  • 4. Further evidence for genetic heterogeneity in the fragile X syndrome.
    Brown WT, Jenkins EC, Gross AC, Chan CB, Krawczun MS, Duncan CJ, Sklower SL, Fisch GS.
    Hum Genet; 1987 Apr; 75(4):311-21. PubMed ID: 2883105
    [Abstract] [Full Text] [Related]

  • 5. Fragile X syndrome.
    Laxova R.
    Adv Pediatr; 1994 Apr; 41():305-42. PubMed ID: 7992687
    [Abstract] [Full Text] [Related]

  • 6. The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers.
    Fishburn J, Turner G, Daniel A, Brookwell R.
    Am J Med Genet; 1983 Apr; 14(4):713-24. PubMed ID: 6682625
    [Abstract] [Full Text] [Related]

  • 7. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.
    Mulley JC, Gedeon AK, Thorn KA, Bates LJ, Sutherland GR.
    Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048
    [Abstract] [Full Text] [Related]

  • 8. The fragile X syndrome (Martin-Bell syndrome). Clinical and cytogenetic findings in 16 prepubertal boys and in 4 of their 5 families.
    Schinzel A, Largo RH.
    Helv Paediatr Acta; 1985 Jul; 40(2-3):133-52. PubMed ID: 3843245
    [Abstract] [Full Text] [Related]

  • 9. 46,XY/47,XYY male with the fragile X syndrome: cytogenetic and molecular studies.
    Milunsky A, Huang X, Amos JA, Herskowitz J, Farrer LA, Wyandt HE.
    Am J Med Genet; 1993 Mar 01; 45(5):589-93. PubMed ID: 8096117
    [Abstract] [Full Text] [Related]

  • 10. X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families).
    Rocchi M, Archidiacono N, Filippi G.
    J Genet Hum; 1987 Dec 01; 35(5):351-79. PubMed ID: 3437265
    [Abstract] [Full Text] [Related]

  • 11. Fragile X frequency in a mentally retarded population in Brazil.
    Mingroni-Netto RC, Rosenberg C, Vianna-Morgante AM, Pavanello Rde C.
    Am J Med Genet; 1990 Jan 01; 35(1):22-7. PubMed ID: 2301469
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  • 17. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males.
    Soudek D, Partington MW, Lawson JS.
    Am J Med Genet; 1984 Jan 01; 17(1):241-52. PubMed ID: 6711598
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  • 18. Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).
    Turner G, Brookwell R, Daniel A, Selikowitz M, Zilibowitz M.
    N Engl J Med; 1980 Sep 18; 303(12):662-4. PubMed ID: 6931286
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  • 19. Molecular diagnosis of the fragile X [Fra (X)] syndrome: calculation of risks based on flanking DNA markers in small phase-unknown families.
    Bridge PJ, Lillicrap DP.
    Am J Med Genet; 1989 May 18; 33(1):92-9. PubMed ID: 2568753
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  • 20. X-linked mental retardation.
    Fryns JP.
    Prog Clin Biol Res; 1985 May 18; 177():309-19. PubMed ID: 2409559
    [No Abstract] [Full Text] [Related]

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