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Fecha de publicación	Título	Autor(es)
2001	Alterations of cell cycle regulators affecting the RB pathway in nonfamilial retinoblastoma	Orjuela M.,
2012	Análisis del gen metilmalonil-CoA mutasa en diez pacientes mexicanos con acidemia metilmalónica	Méndez ST
2015	Association between two polymorphisms of histamine-metabolising enzymes and the severity of allergic rhinitis in a group of Mexican children	Meza Velázquez, MR
2014	ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA	Bahena Bahena D.,
2013	Clinical and genetic analysis of patients with X-linked hyper-IgM syndrome	Vargas Hernadez A
2002	New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia	Machuca Tzili L
2015	Phenylalanine hydroxylase deficiency in Mexico: Genotype-phenotype correlations, BH<inf>4</inf> responsiveness and evidence of a founder effect	Vela Amieva, Marcela Beatríz
2011	Prenatal diagnosis in a cystic fibrosis family: A combined molecular strategy for a precise diagnosis	Chávez Saldaña, Margarita

Mostrando resultados 1 a 8 de 8