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Journal Abstract Search

142 related items for PubMed ID: 574718

  • 1. Christ-Siemens-Touraine syndrome--a clinical and genetic analysis of a large Brazilian kindred: II. Affected males.
    Pinheiro M, Freire-Maia N.
    Am J Med Genet; 1979; 4(2):123-8. PubMed ID: 574718
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  • 2. Christ-Siemens-Touraine syndrome--a clinical and genetic analysis of a large Brazilian kindred: I. Affected females.
    Pinheiro M, Freire-Maia N.
    Am J Med Genet; 1979; 4(2):113-22. PubMed ID: 517571
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  • 3. Christ-Siemens-Touraine syndrome--a clinical and genetic analysis of a large Brazilian kindred: III. Carrier detection.
    Pinheiro M, Freire-Maia N.
    Am J Med Genet; 1979; 4(2):129-34. PubMed ID: 517572
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  • 6. A rare case of tooth-nail syndrome.
    Mielnik-Błaszczak M, Tomankiewicz M.
    Ann Univ Mariae Curie Sklodowska Med; 2003; 58(2):306-10. PubMed ID: 15323210
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  • 7. Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia.
    Fadhil M, Ghabra TA, Deeb M, Der Kaloustian VM.
    Am J Med Genet; 1983 Feb; 14(2):335-46. PubMed ID: 6837628
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  • 9. [Anhidrotic ectodermal dysplasia (Christ-Siemens-Touraine-Syndrome) in an x-linked recessive mode of inheritance (author's transl)].
    Kuhlwein A, Weiss J.
    Dermatol Monatsschr; 1982 Jan; 168(1):34-43. PubMed ID: 7200917
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  • 10. Mosaic expression of hypohidrotic ectodermal dysplasia in an isolated affected female child.
    Bartstra HL, Hulsmans RF, Steijlen PM, Ruige M, de Die-Smulders CE, Cassiman JJ.
    Arch Dermatol; 1994 Nov; 130(11):1421-4. PubMed ID: 7979445
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  • 11. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia.
    Propping P, Zerres K.
    Am J Med Genet; 1993 Mar 01; 45(5):642-8. PubMed ID: 8456838
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  • 13. A Rapp-Hodgkin like syndrome in three sibs: clinical, dental and dermatoglyphic study.
    Atasu M, Akesi S, Elçioglu N, Yatmaz PI, Ertas EB.
    Clin Dysmorphol; 1999 Apr 01; 8(2):101-10. PubMed ID: 10319198
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  • 14. Pure hair-nail ectodermal dysplasia maps to chromosome 12p11.1-q21.1 in a consanguineous Pakistani family.
    Naeem M, John P, Ali G, Ahmad W.
    Clin Exp Dermatol; 2007 Sep 01; 32(5):502-5. PubMed ID: 17489990
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  • 17. Facial morphometrics in the identification of gene carriers of X-linked hypohidrotic ectodermal dysplasia.
    Saksena SS, Bixler D.
    Am J Med Genet; 1990 Jan 01; 35(1):105-14. PubMed ID: 2301459
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  • 18. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
    Tariq M, Chishti MS, Ali G, Ahmad W.
    Ann Hum Genet; 2008 Jan 01; 72(Pt 1):19-25. PubMed ID: 18184143
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