Ma. Luisa Ordóñez-Sánchez

Early-Onset Type 2 Diabetes: Metabolic and Genetic Characterization in the Mexican Population¹

Carlos A. Aguilar‐Salinas, Eduardo Reyes-Rodríguez, Ma. Luisa Ordóñez-Sánchez et al. · The Journal of Clinical Endocrinology & Metabolism · 2001 · 51 citations · Full text

Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease.

Antonio Ulises López-Gutierrez, Laura Riba, Ma. Luisa Ordóñez-Sánchez et al. · Journal of Medical Genetics · 1998 · 33 citations · Full text

Genetics, Mexican Families, Pathology +16

Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population: Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease

Mark N. Lobato, Ma. Luisa Ordóñez-Sánchez, M T Tusié-Luna et al. · Human Heredity · 1999 · 30 citations

The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-size adipocytes

Paloma Almeda‐Valdés, Donají Gómez‐Velasco, Olimpia Arellano Campos et al. · European Journal of Endocrinology · 2018 · 25 citations

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

Marı́a Teresa Tusié-Luna, Salvador Ramı́rez-Jiménez, Ma. Luisa Ordóñez-Sánchez et al. · Human Genetics · 1996 · 21 citations

Mexican Population, Mendelian Disorder, Genetic Disorder +8