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Journal Abstract Search

284 related items for PubMed ID: 4041576

  • 21.
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  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. [Adams-Oliver syndrome].
    Ishikiriyama S.
    Ryoikibetsu Shokogun Shirizu; 1996 Oct 31; (15):234-5. PubMed ID: 9047997
    [No Abstract] [Full Text] [Related]

  • 24. Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation.
    Yağci-Küpeli B, Çağlar K, Büyük S, Balci S.
    Genet Couns; 2011 Oct 31; 22(1):55-61. PubMed ID: 21614989
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  • 25. Scalp-ear-nipple syndrome: additional manifestations.
    Edwards MJ, McDonald D, Moore P, Rae J.
    Am J Med Genet; 1994 Apr 15; 50(3):247-50. PubMed ID: 8042668
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  • 29. Polymicrogyria associated with scalp and limb defects: variant of Adams-Oliver syndrome.
    Amor DJ, Leventer RJ, Hayllar S, Bankier A.
    Am J Med Genet; 2000 Aug 14; 93(4):328-34. PubMed ID: 10946361
    [Abstract] [Full Text] [Related]

  • 30. Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome: an additional clinical observation.
    Hoyme HE, Der Kaloustian VM, Hogg H, Entin MA, Guttmacher AE.
    Am J Med Genet; 1992 Feb 01; 42(3):398-9. PubMed ID: 1536190
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  • 31.
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  • 33. The wide spectrum of clinical expression in Adams-Oliver syndrome: a report of two cases.
    Mempel M, Abeck D, Lange I, Strom K, Caliebe A, Beham A, Kautza M, Worret WI, Neubauer BA, Ring J, Schröder H, Fölster-Holst R.
    Br J Dermatol; 1999 Jun 01; 140(6):1157-60. PubMed ID: 10354089
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  • 34. Familial brachydactyly and chondrocalcinosis. Report of a patient, pedigree and review of the literature.
    Mathews JL, Samuelson CO, Manis S.
    J Rheumatol; 1983 Oct 01; 10(5):819-22. PubMed ID: 6644710
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  • 38. [Aplasia cutis congenita in 4 infants].
    Beekmans SJ, Haumann TJ, Vandertop WP, Mulder JW.
    Ned Tijdschr Geneeskd; 2002 Sep 28; 146(39):1842-5. PubMed ID: 12382371
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  • 39. The Greig cephalopolysyndactyly syndrome in a Canadian family.
    Chudley AE, Houston CS.
    Am J Med Genet; 1982 Nov 28; 13(3):269-76. PubMed ID: 6295159
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