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Journal Abstract Search

182 related items for PubMed ID: 3163892

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker.
    Hanauer A, Alembik Y, Arveiler B, Formiga L, Gilgenkrantz S, Mandel JL.
    Hum Genet; 1988 Oct; 80(2):177-80. PubMed ID: 2902000
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis.
    Zonana J, Schinzel A, Upadhyaya M, Thomas NS, Anton-Lamprecht I, Harper PS.
    Am J Med Genet; 1990 Jan; 35(1):132-5. PubMed ID: 2301463
    [Abstract] [Full Text] [Related]

  • 4. X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization.
    Clarke A, Sarfarazi M, Thomas NS, Roberts K, Harper PS.
    Hum Genet; 1987 Apr; 75(4):378-80. PubMed ID: 2883107
    [Abstract] [Full Text] [Related]

  • 5. Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome).
    MacDermot KD, Winter RM, Malcolm S.
    Hum Genet; 1986 Oct; 74(2):172-3. PubMed ID: 3464559
    [Abstract] [Full Text] [Related]

  • 6. Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.
    Lesko JG, Lewis RA, Nussbaum RL.
    Am J Hum Genet; 1987 Apr; 40(4):303-11. PubMed ID: 2883887
    [Abstract] [Full Text] [Related]

  • 7. Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis.
    Zonana J, Sarfarazi M, Thomas NS, Clarke A, Marymee K, Harper PS.
    J Pediatr; 1989 Mar; 114(3):392-9. PubMed ID: 2564048
    [Abstract] [Full Text] [Related]

  • 8. High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus.
    Zonana J, Jones M, Browne D, Litt M, Kramer P, Becker HW, Brockdorff N, Rastan S, Davies KP, Clarke A.
    Am J Hum Genet; 1992 Nov; 51(5):1036-46. PubMed ID: 1357963
    [Abstract] [Full Text] [Related]

  • 9. Multipoint linkage analysis in Menkes disease.
    Tønnesen T, Petterson A, Kruse TA, Gerdes AM, Horn N.
    Am J Hum Genet; 1992 May; 50(5):1012-7. PubMed ID: 1570830
    [Abstract] [Full Text] [Related]

  • 10. Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome.
    Greer WL, Somani AK, Kwong PC, Peacocke M, Rubin LA, Siminovitch KA.
    Genomics; 1990 Mar; 6(3):568-71. PubMed ID: 2328995
    [Abstract] [Full Text] [Related]

  • 11. Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome.
    Arveiler B, Oberlé I, Mandel JL.
    Genomics; 1987 Sep; 1(1):60-6. PubMed ID: 2889662
    [Abstract] [Full Text] [Related]

  • 12. Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasia.
    Goodship J, Malcolm S, Clarke A, Pembrey ME.
    J Med Genet; 1990 Jul; 27(7):422-5. PubMed ID: 2395159
    [Abstract] [Full Text] [Related]

  • 13. Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.
    de Saint Basile G, Arveiler B, Oberlé I, Malcolm S, Levinsky RJ, Lau YL, Hofker M, Debre M, Fischer A, Griscelli C.
    Proc Natl Acad Sci U S A; 1987 Nov; 84(21):7576-9. PubMed ID: 3478714
    [Abstract] [Full Text] [Related]

  • 14. X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.
    Puck JM, Nussbaum RL, Smead DL, Conley ME.
    Am J Hum Genet; 1989 May; 44(5):724-30. PubMed ID: 2565084
    [Abstract] [Full Text] [Related]

  • 15. Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male.
    Goodship J, Levinsky R, Malcolm S.
    Hum Genet; 1989 Dec; 84(1):11-4. PubMed ID: 2606471
    [Abstract] [Full Text] [Related]

  • 16. Refinement of linkage of human severe combined immunodeficiency (SCIDX1) to polymorphic markers in Xq13.
    Puck JM, Conley ME, Bailey LC.
    Am J Hum Genet; 1993 Jul; 53(1):176-84. PubMed ID: 8317482
    [Abstract] [Full Text] [Related]

  • 17. Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13.
    Beckett J, Holden JJ, Simpson NE, White BN, MacLeod PM.
    J Neurogenet; 1986 Jul; 3(4):225-31. PubMed ID: 3462379
    [Abstract] [Full Text] [Related]

  • 18. Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder.
    Munoz F, Lestringant G, Sybert V, Frydman M, Alswaini A, Frossard PM, Jorgenson R, Zonana J.
    Am J Hum Genet; 1997 Jul; 61(1):94-100. PubMed ID: 9245989
    [Abstract] [Full Text] [Related]

  • 19. Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA).
    Thomas NS, Chelly J, Zonana J, Davies KJ, Morgan S, Gault J, Rack KA, Buckle VJ, Brockdorff N, Clarke A.
    Hum Mol Genet; 1993 Oct; 2(10):1679-85. PubMed ID: 8268921
    [Abstract] [Full Text] [Related]

  • 20. Hypohidrotic (anhidrotic) ectodermal dysplasia: molecular genetic research and its clinical applications.
    Zonana J.
    Semin Dermatol; 1993 Sep; 12(3):241-6. PubMed ID: 8217562
    [Abstract] [Full Text] [Related]

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