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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

122 related items for PubMed ID: 9429137

  • 1. Muscular involvement in the Holt-Oram syndrome.
    Spranger S, Ulmer H, Tröger J, Jansen O, Graf J, Meinck HM, Spranger M.
    J Med Genet; 1997 Dec; 34(12):978-81. PubMed ID: 9429137
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  • 2. The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome).
    Basson CT, Cowley GS, Solomon SD, Weissman B, Poznanski AK, Traill TA, Seidman JG, Seidman CE.
    N Engl J Med; 1994 Mar 31; 330(13):885-91. PubMed ID: 8114858
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  • 3. Genetic heterogeneity of heart-hand syndromes.
    Basson CT, Solomon SD, Weissman B, MacRae CA, Poznanski AK, Prieto F, Ruiz de la Fuente S, Pease WE, Levin SE, Holmes LB.
    Circulation; 1995 Mar 01; 91(5):1326-9. PubMed ID: 7867169
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  • 4. [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 Mar 01; 135(4):368-75. PubMed ID: 9381776
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  • 5. [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 01; 88(5):661-6. PubMed ID: 7646274
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  • 6. Holt-Oram syndrome: a clinical genetic study.
    Newbury-Ecob RA, Leanage R, Raeburn JA, Young ID.
    J Med Genet; 1996 Apr 01; 33(4):300-7. PubMed ID: 8730285
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  • 9. [Variants of radial hemimelia with and without vitium cordis (Holt-Oram syndrome) in 2 families].
    Pfeiffer RA, Böwing B, Deeg KH.
    Monatsschr Kinderheilkd; 1989 May 01; 137(5):275-9. PubMed ID: 2739665
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  • 11. Heart-hand syndrome II. A report of Tabatznik syndrome with new findings.
    Silengo MC, Biagioli M, Guala A, Lopez-Bell G, Lala R.
    Clin Genet; 1990 Aug 01; 38(2):105-13. PubMed ID: 1976459
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  • 13. [Genetical basis of Holt-Oram syndrome].
    Rokicka A, Rokicki W.
    Wiad Lek; 1999 Aug 01; 52(11-12):606-9. PubMed ID: 10745699
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  • 19. Molecular characterization of a 14q deletion in a boy with features of Holt-Oram syndrome.
    Le Meur N, Goldenberg A, Michel-Adde C, Drouin-Garraud V, Blaysat G, Marret S, Amara SA, Moirot H, Joly-Hélas G, Mace B, Kleinfinger P, Saugier-Veber P, Frébourg T, Rossi A.
    Am J Med Genet A; 2005 May 01; 134(4):439-42. PubMed ID: 15810003
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