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
ORDONEZ-SANCHEZ, M. L, RAMIREZ-JIMENEZ, S, TUSIE-LUNA, M. T, LOPEZ-GUTIERREZ, A. U, RIBA, L, GAMBOA-CARDIEL, S, CERRILLO-HINOJOSA, M, ALTAMIRANO-BUSTAMANTE, N, CALZADA-LEON, R, ROBLES-VALDES, C, MENDOZA-MORFIN, F
Published in Human genetics (01.02.1998)
Published in Human genetics (01.02.1998)
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Journal Article
Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease
López-Gutiérrez, A U, Riba, L, Ordoñez-Sánchez, M L, Ramírez-Jiménez, S, Cerrillo-Hinojosa, M, Tusié-Luna, M T
Published in Journal of medical genetics (01.12.1998)
Published in Journal of medical genetics (01.12.1998)
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Proposed normal values for alpha fetoprotein in maternal serum for the detection of neural tube closure defects and Down syndrome. Preliminary study
Carreras de Paz, J J, Silva Mendoza, J M, Violante Diaz, M, Cerrillo Hinojosa, M, Ahued Ahued, J R
Published in Ginecologia y obstetricia de Mexico (01.08.1991)
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Published in Ginecologia y obstetricia de Mexico (01.08.1991)
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