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Journal Abstract Search

150 related items for PubMed ID: 7471507

  • 1. Athelia in a female infant - heterozygous for anhidrotic ectodermal dysplasia.
    Burck U, Held KR.
    Clin Genet; 1981 Feb; 19(2):117-21. PubMed ID: 7471507
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  • 2. [Anhidrotic ectodermal dysplasia (apropos of 3 families). Abnormal hair, a sign of heterozygosity?].
    Le Marec B, Roussey M, Chevrant-Breton J, Segalen J, Bourdinière J, Sénécal J.
    J Genet Hum; 1983 Dec; 31(4):279-93. PubMed ID: 6663288
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  • 3. [Anhidrotic ectodermal dysplasia--Identification of heterocygote (carrier) females (author's transl)].
    Messow K, Götz A, Murken JD, Rodewald A, Riegel K.
    Z Geburtshilfe Perinatol; 1977 Apr; 181(2):129-33. PubMed ID: 878540
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  • 4. [Anhidrotic ectodermal dysplasia. Clinico-genetic study of 4 families].
    Balestrazzi P, Solli R, Salami P, Corrini L, Mattioli M, Bernasconi S.
    Minerva Pediatr; 1979 Feb 28; 31(4):265-74. PubMed ID: 460084
    [No Abstract] [Full Text] [Related]

  • 5. A previously undescribed ectodermal dysplasia of the tricho-odonto-onychial subgroup in a family.
    Tsakalakos N, Jordaan FH, Taljaard JJ, Hough SF.
    Arch Dermatol; 1986 Sep 28; 122(9):1047-53. PubMed ID: 3740884
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  • 6. Anhidrotic (or hypohidrotic) ectodermal dysplasis.
    Martin-Pascual A, De Unamuno P, Aparicio M, Herreros V.
    Dermatologica; 1977 Sep 28; 154(4):235-43. PubMed ID: 140825
    [No Abstract] [Full Text] [Related]

  • 7. Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features.
    Anton-Lamprecht I, Schleiermacher E, Wolf M.
    Birth Defects Orig Artic Ser; 1988 Sep 28; 24(2):183-95. PubMed ID: 3179426
    [No Abstract] [Full Text] [Related]

  • 8. Expression of X-linked hypohidrotic ectodermal dysplasia in six males and in their mothers.
    Söderholm AL, Kaitila I.
    Clin Genet; 1985 Aug 28; 28(2):136-44. PubMed ID: 4042395
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  • 16. Brief clinical report: new, autosomal dominant form of ectodermal dysplasia.
    Tuffli GA, Laxova R.
    Am J Med Genet; 1983 Feb 28; 14(2):381-4. PubMed ID: 6837633
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  • 18. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein.
    Kere J, Srivastava AK, Montonen O, Zonana J, Thomas N, Ferguson B, Munoz F, Morgan D, Clarke A, Baybayan P, Chen EY, Ezer S, Saarialho-Kere U, de la Chapelle A, Schlessinger D.
    Nat Genet; 1996 Aug 28; 13(4):409-16. PubMed ID: 8696334
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  • 19. Hereditary hypodontia and onychorrhexis of the fingernails and toenail koilonychia: Witkop's tooth-and nail syndrome.
    Zabawski EJ, Cohen JB.
    Dermatol Online J; 1999 May 28; 5(1):3. PubMed ID: 10673446
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  • 20. [Anhidrotic ectodermal dysplasia. Apropos of a case report of quadruplets].
    Delaire J, Schmidt J, Lumineau JP, Pressard J, Billet J.
    Rev Stomatol Chir Maxillofac; 1984 May 28; 85(1):34-7. PubMed ID: 6584956
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