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PUBMED FOR HANDHELDS

Journal Abstract Search


198 related items for PubMed ID: 9803503

  • 1. [Type II lissencephaly: presentation of intermediate form].
    Palomero-Domínguez MA, Ramos-Fernández JM, Domínguez-Santurino F, Ruiz-Gómez M.
    Rev Neurol; 1998 Oct; 27(158):594-6. PubMed ID: 9803503
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  • 5. Diagnostic criteria for Walker-Warburg syndrome.
    Dobyns WB, Pagon RA, Armstrong D, Curry CJ, Greenberg F, Grix A, Holmes LB, Laxova R, Michels VV, Robinow M.
    Am J Med Genet; 1989 Feb; 32(2):195-210. PubMed ID: 2494887
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  • 8. [Walker-Warburg syndrome: cerebro-ocular dysgenesis and congenital muscular dystrophy].
    Macaya Ruiz A, Roig Quilis M, Sancho Olivé S, Navarro Fernández-Valbuena C, Tallada Serra M, Olesti Marco M.
    An Esp Pediatr; 1989 Nov; 31(5):465-9. PubMed ID: 2619134
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  • 10. Clinical spectrum and genetic studies of Fukuyama congenital muscular dystrophy.
    Yoshioka M, Kuroki S.
    Am J Med Genet; 1994 Nov 15; 53(3):245-50. PubMed ID: 7856660
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  • 11. Lissencephaly with congenital muscular dystrophy and ocular abnormalities: cerebro-oculo-muscular syndrome.
    Sasaki M, Yoshioka K, Yanagisawa T, Nemoto A, Takasago Y, Nagano T.
    Childs Nerv Syst; 1989 Feb 15; 5(1):35-7. PubMed ID: 2495176
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  • 14. Walker-Warburg syndrome with microtia and absent auditory canals.
    Gershoni-Baruch R, Mandel H, Miller B, Sujov P, Braun J.
    Am J Med Genet; 1990 Sep 15; 37(1):87-91. PubMed ID: 2240049
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  • 15. A case of Walker-Warburg syndrome resulting from a homozygous POMT1 mutation.
    Yis U, Uyanik G, Kurul S, Dirik E, Ozer E, Gross C, Hehr U.
    Eur J Paediatr Neurol; 2007 Jan 15; 11(1):46-9. PubMed ID: 17161965
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