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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

99 related items for PubMed ID: 5710712

  • 1. Ectodermal dysplasia--a new variant?
    Bartalos M, Saraçli T.
    J Genet Hum; 1968 Jan; 16(3):49-56. PubMed ID: 5710712
    [No Abstract] [Full Text] [Related]

  • 2. Hereditary anhidrotic ectodermal dysplasia in a Zambian family.
    Sehgal D, Chawla V, Maguire MJ.
    East Afr Med J; 1981 May; 58(5):374-9. PubMed ID: 7285838
    [No Abstract] [Full Text] [Related]

  • 3. [Dental disorders in anhidrotic ectodermal dysplasia].
    Rezsö B.
    Fogorv Sz; 1978 Jan; 71(1):26-8. PubMed ID: 272997
    [No Abstract] [Full Text] [Related]

  • 4. Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child.
    Moerman P, Fryns JP.
    Am J Med Genet; 1996 Jun 14; 63(3):479-81. PubMed ID: 8737656
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  • 5. Variant of odontoonychodermal dysplasia?
    Arnold WP, Merkx MA, Steijlen PM.
    Am J Med Genet; 1995 Nov 06; 59(2):242-4. PubMed ID: 8588594
    [No Abstract] [Full Text] [Related]

  • 6. [Familial split hand and foot, cleft lip and palate, ectodermal dysplasia syndrome].
    Szappanos L, Czeizel E, Szepesi K.
    Orv Hetil; 1984 Mar 11; 125(11):633-8. PubMed ID: 6700970
    [No Abstract] [Full Text] [Related]

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  • 9. A de novo heterozygous point mutation in the p63 gene causing the syndrome of ectrodactyly, ectodermal dysplasia and facial clefting.
    Pozo G, Canún S, Kofman-Alfaro S, Zenteno JC.
    Br J Dermatol; 2004 Oct 11; 151(4):930-2. PubMed ID: 15491445
    [No Abstract] [Full Text] [Related]

  • 10. [Anodontic anhydrotic ectodermal dysplasia].
    Jourdain JC, Lelorier B, Larrègue M.
    Ann Dermatol Venereol; 1984 Oct 11; 111(10):939-40. PubMed ID: 6524811
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  • 13. Premature cataracts in a family with hidrotic ectodermal dysplasia.
    Hazen PG, Zamora I, Bruner WE, Muir WA.
    Arch Dermatol; 1980 Dec 11; 116(12):1385-7. PubMed ID: 7458367
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  • 14. Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene.
    Rinne T, Spadoni E, Kjaer KW, Danesino C, Larizza D, Kock M, Huoponen K, Savontaus ML, Aaltonen M, Duijf P, Brunner HG, Penttinen M, van Bokhoven H.
    Eur J Hum Genet; 2006 Aug 11; 14(8):904-10. PubMed ID: 16724007
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  • 15. A single maxillary incisor as a manifestation of an ectodermal dysplasia.
    Buntinx I, Baraitser M.
    J Med Genet; 1989 Oct 11; 26(10):648-51. PubMed ID: 2585463
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  • 16. De novo missense mutation, S541Y, in the p63 gene underlying Rapp-Hodgkin ectodermal dysplasia syndrome.
    Shotelersuk V, Janklat S, Siriwan P, Tongkobpetch S.
    Clin Exp Dermatol; 2005 May 11; 30(3):282-5. PubMed ID: 15807690
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  • 17. [Familial ectodermal dysplasia with agenesis of the breasts and the external urethral sphincter. Description of a case].
    Triolo O, Allegra A, Stella Brienza L, De Meo A, Tropea G.
    Minerva Ginecol; 1993 Mar 11; 45(3):139-42. PubMed ID: 8332280
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  • 20. [Clinical and genetic studies of a family with ectodermal dysplasia].
    Gajewska-Obel E, Kozlowska M.
    Pol Tyg Lek; 1976 Mar 22; 31(12):491-2. PubMed ID: 1272936
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