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Journal Abstract Search

239 related items for PubMed ID: 8042668

  • 21. Adams-Oliver syndrome and isolated aplasia cutis congenita in two siblings.
    Rajabian MH, Aghaei S.
    Dermatol Online J; 2006 Oct 31; 12(6):17. PubMed ID: 17083897
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  • 22. A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation.
    Caksen H, Kurtoğlu S.
    Acta Neurol Belg; 2000 Dec 31; 100(4):252-5. PubMed ID: 11233683
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  • 24. Familial aplasia cutis congenita and coarctation of the aorta.
    Dallapiccola B, Giannotti A, Marino B, Digilio C, Obregon G.
    Am J Med Genet; 1992 Jul 01; 43(4):762-3. PubMed ID: 1621771
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  • 26. [Scalp-ear-nipple syndrome].
    Sonoda T.
    Ryoikibetsu Shokogun Shirizu; 2001 Jul 01; (34 Pt 2):606-7. PubMed ID: 11528920
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  • 27. Molecular basis of the scalp-ear-nipple syndrome unraveled by the characterization of disease-causing KCTD1 mutants.
    Smaldone G, Balasco N, Pirone L, Caruso D, Di Gaetano S, Pedone EM, Vitagliano L.
    Sci Rep; 2019 Jul 19; 9(1):10519. PubMed ID: 31324836
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  • 30. Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance.
    Koiffmann CP, Wajntal A, Huyke BJ, Castro RM.
    Am J Med Genet; 1988 Feb 19; 29(2):263-8. PubMed ID: 3354597
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  • 36. Aplasia cutis congenita.
    Deeken JH, Caplan RM.
    Arch Dermatol; 1970 Oct 19; 102(4):386-9. PubMed ID: 5536130
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  • 38. Type III syndactyly and oculodentodigital dysplasia: a clinical spectrum.
    Schrander-Stumpel CT, De Groot-Wijnands JB, De Die-Smulders C, Fryns JP.
    Genet Couns; 1993 Oct 19; 4(4):271-6. PubMed ID: 8110413
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  • 40. A distinct type of hidrotic ectodermal dysplasia.
    Halal F, Setton N, Wang NS.
    Am J Med Genet; 1991 Mar 15; 38(4):552-6. PubMed ID: 2063897
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