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PUBMED FOR HANDHELDS

Journal Abstract Search

169 related items for PubMed ID: 8110414

  • 1. Holt-Oram syndrome: postaxial and central polydactyly as variable manifestations in a four generations family.
    Moens P, De Smet L, Fabry G, Fryns JP.
    Genet Couns; 1993; 4(4):277-80. PubMed ID: 8110414
    [No Abstract] [Full Text] [Related]

  • 2. Holt-Oram syndrome with associated postaxial and central polydactyly. Further evidence for genetic heterogeneity in the Holt-Oram syndrome.
    Fryns JP, Bonnet D, De Smet L.
    Genet Couns; 1996; 7(4):323-4. PubMed ID: 8985738
    [No Abstract] [Full Text] [Related]

  • 3. Variation in severity of cardiac disease in Holt-Oram syndrome.
    Sletten LJ, Pierpont ME.
    Am J Med Genet; 1996 Oct 16; 65(2):128-32. PubMed ID: 8911604
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  • 4. [Association of the Holt-Oram syndrome (digito-atrial dysplasia) and mitral prolapse in a family].
    Di Luzio V, Blandini A, Ballerini L, Purcaro A.
    G Ital Cardiol; 1981 Oct 16; 11(10):1548-55. PubMed ID: 7341325
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  • 5. 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 16; 22(1):55-61. PubMed ID: 21614989
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  • 7. [Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome].
    Bonnet D, Terrett J, Pequignot-Viegas E, Weissenbach J, Munnich A, Lyonnet S, Kachaner J.
    Arch Mal Coeur Vaiss; 1995 May 16; 88(5):661-6. PubMed ID: 7646274
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  • 11. Triphalangeal thumb and psychomotor retardation: a new association?
    Rodriguez-Rojas LX, Macias NM, Barros-Nuñez P.
    Genet Couns; 2003 May 16; 14(1):39-43. PubMed ID: 12725588
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  • 12. [The Holt-Oram syndrome. Review of the literature and current orthopedic treatment concepts].
    Weber M, Wenz W, van Riel A, Kaufmann A, Graf J.
    Z Orthop Ihre Grenzgeb; 1997 May 16; 135(4):368-75. PubMed ID: 9381776
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  • 13. Polydactyly with ectodermal defect, osteopenia, and mental delay.
    Zannolli R, Buoni S, Viviano M, Macucci F, D'Ambrosio A, Livi W, Mazzei MA, Mazzei F, Sacco P, Volterrani L, Vonella G, Orsi A, Zappella M, Hayek J.
    J Child Neurol; 2008 Jun 16; 23(6):683-9. PubMed ID: 18182642
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  • 17. [A case of Holt-Oram syndrome].
    Martin C, Babin JP, San Juan B, Hehunstre JP.
    Bord Med; 1970 Oct 16; 3(10):2464. PubMed ID: 5480226
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  • 19. [Holt-Oram syndrome: family affected without TBX5 mutation and without phenotype manifestations in a probable mutation carrier].
    Murga-Eizagaechevarria N, Garcia-Barcina M, Sarasola Diez E.
    Rev Esp Cardiol; 2011 Dec 16; 64(12):1225-6. PubMed ID: 21752519
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  • 20. "Holoprosencephaly-polydactyly" (pseudotrisomy 13) syndrome: expansion of the phenotypic spectrum.
    Lurie IW, Wulfsberg EA.
    Am J Med Genet; 1993 Sep 01; 47(3):405-9. PubMed ID: 8135289
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