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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]