1. Instituto Nacional de Pediatría

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Fecha de publicaciónTítuloAutor(es)
2015Association between two polymorphisms of histamine-metabolising enzymes and the severity of allergic rhinitis in a group of Mexican childrenMeza Velázquez, MR
2015Association of HMOX1 and NQO1 polymorphisms with metabolic syndrome componentsMartínez Hernández A
2012Consequences of two naturally occurring missense mutations in the structure and function of Bruton agammaglobulinemia tyrosine kinaseVargas Hernández A
2013IL-12Rβ1 deficiency: Mutation update and description of the IL12RB1 variation databaseVan De Vosse Esther
2014Interstitial deletion of 2q24.2: Further delineation of an emerging syndrome associated with intellectual disability, severe hypotonia and moderate intrauterine growth restrictionYokoyama Rebollar, Emiy
2015Phenylalanine hydroxylase deficiency in Mexico: Genotype-phenotype correlations, BH<inf>4</inf> responsiveness and evidence of a founder effectVela Amieva, Marcela Beatríz
Mostrando resultados 1 a 6 de 6