These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

194 related items for PubMed ID: 2564048

  • 1. 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]

  • 2. 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]

  • 3. X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.
    Zonana J, Clarke A, Sarfarazi M, Thomas NS, Roberts K, Marymee K, Harper PS.
    Am J Hum Genet; 1988 Jul; 43(1):75-85. PubMed ID: 3163892
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 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. 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]

  • 7. 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]

  • 8. Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12.
    Kølvraa S, Kruse TA, Jensen PK, Linde KH, Vestergaard SR, Bolund L.
    Hum Genet; 1986 Nov; 74(3):284-7. PubMed ID: 2877938
    [Abstract] [Full Text] [Related]

  • 9. A dental approach to carrier screening in X linked hypohidrotic ectodermal dysplasia.
    Spfaer JA.
    J Med Genet; 1981 Dec; 18(6):459-60. PubMed ID: 7334506
    [Abstract] [Full Text] [Related]

  • 10. Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia.
    Crawford PJ, Aldred MJ, Clarke A.
    J Med Genet; 1991 Mar; 28(3):181-5. PubMed ID: 2051453
    [Abstract] [Full Text] [Related]

  • 11. Hypohidrotic ectodermal dysplasia: argument against an autosomal recessive form clinically indistinguishable from X-linked hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome).
    Sybert VP.
    Pediatr Dermatol; 1989 Jun; 6(2):76-81. PubMed ID: 2748478
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia.
    Cambiaghi S, Restano L, Pääkkönen K, Caputo R, Kere J.
    Arch Dermatol; 2000 Feb; 136(2):217-24. PubMed ID: 10677098
    [Abstract] [Full Text] [Related]

  • 14. A novel missense mutation (402C-->T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasia.
    Hertz JM, Nørgaard Hansen K, Juncker I, Kjeldsen M, Gregersen N.
    Clin Genet; 1998 Mar; 53(3):205-9. PubMed ID: 9630076
    [Abstract] [Full Text] [Related]

  • 15. Manifestation of the lines of Blaschko in women heterozygous for X-linked hypohidrotic ectodermal dysplasia.
    Happle R, Frosch PJ.
    Clin Genet; 1985 May; 27(5):468-71. PubMed ID: 4006271
    [Abstract] [Full Text] [Related]

  • 16. A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia.
    Nakata M, Koshiba H, Eto K, Nance WE.
    Am J Hum Genet; 1980 Nov; 32(6):908-19. PubMed ID: 7446529
    [Abstract] [Full Text] [Related]

  • 17. Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications.
    Ferguson BM, Thomas NS, Munoz F, Morgan D, Clarke A, Zonana J.
    J Med Genet; 1998 Feb; 35(2):112-5. PubMed ID: 9507389
    [Abstract] [Full Text] [Related]

  • 18. Hypodontia and sweat pore counts in detecting carriers of X-linked hypohidrotic ectodermal dysplasia.
    Sofaer JA.
    Br Dent J; 1981 Nov 17; 151(10):327-30. PubMed ID: 6946797
    [No Abstract] [Full Text] [Related]

  • 19. Hypohidrotic ectodermal dysplasia. Clinical study of a family of 30 over three generations.
    Gilgenkrantz S, Blanchet-Bardon C, Nazzaro V, Formiga L, Mujica P, Alembik Y.
    Hum Genet; 1989 Jan 17; 81(2):120-2. PubMed ID: 2912882
    [Abstract] [Full Text] [Related]

  • 20. Hypohidrotic (anhidrotic) ectodermal dysplasia: molecular genetic research and its clinical applications.
    Zonana J.
    Semin Dermatol; 1993 Sep 17; 12(3):241-6. PubMed ID: 8217562
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.