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PUBMED FOR HANDHELDS

Journal Abstract Search

197 related items for PubMed ID: 2877938

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  • 6. 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
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  • 10. 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
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  • 13. Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment.
    Zonana J, Gault J, Davies KJ, Jones M, Browne D, Litt M, Brockdorff N, Rastan S, Clarke A, Thomas NS.
    Am J Hum Genet; 1993 Jan; 52(1):78-84. PubMed ID: 8434608
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  • 16. 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
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