Anales de la Facultad de Medicina
Universidad Nacional Mayor de San Marcos
Copyright© 2001

ISSN 1025 - 5583
Vol. 62, Nº4 - 2001

 

BIBLIOGRAFÍA

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9) Elejalde BR. Genetic and diagnostic considerations in three families with abnormalities of facial expression and congenital urinary obstruction: "The Ochoa syndrome". Am J Med Genet 1979; 3:97-108.

10) Ochoa B, Gorlin RJ. Urofacial syndrome. Am J Med Genet 1987; 27:661-7.

11) Wang CY, Hawkins-Lee B, Ochoa B, et al. Homozygosity and linkage-disequilibrium mapping of the urofacial (Ochoa) syndrome gene to a 1-cM interval on chromosome 10q23-q24. Am J Hum Genet 1997; 60:1461-7.

12) Wang CY, Huang YQ, Shi JO, et al. Genetic homogeneity, high-resolution mapping, and mutation analysis of urofacial (Ochoa) syndrome and exclusion of the glutamate oxaloacetate transaminase gene (GOT1) in the critical region as the disease gene. Am J Med Genet 1999; 84:454-59.

13) Punal JE, Siebert MF, Anguiera FB, et al. Three new patients with congenital unilateral facial nerve palsy due to chromosome 22q11 deletion. J Child Neurol 2001; 16:450-2.

 

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