F. Mendoza-Morfín

Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: identification of possible new mutations and high prevalence of apparent germ-line mutations

M. Tusié-Luna, L. Riba, R. Calzada-León, 1998, Human Genetics.

Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population

M. Tusié-Luna, J. Cabello-Villegas, R. Calzada-León, 1996, Human Genetics.

Analysis of the glucokinase gene in Mexican families displaying early-onset non-insulin-dependent diabetes mellitus including MODY families.

M. Tusié-Luna, J. Cabello-Villegas, L. Riba, 1997, American journal of medical genetics.