Sergio A. Cuevas‐Covarrubias

Two affected siblings with nuclear cataract associated with a novel missense mutation in the CRYGD gene.

Olga Messina‐Baas, Luz María González-Huerta, Sergio A. Cuevas‐Covarrubias · PubMed · 2006 · 48 citations

Life Sciences, Genetics, Molecular Genetics +15

Gender-specific differences in clinical and metabolic variables associated with NAFLD in a Mexican pediatric population

Eréndira Villanueva-Ortega, María José Garcés-Hernández, Arturo Herrera-Rosas et al. · Annals of Hepatology · 2019 · 42 citations · Full text

Medicine, Child Health, Pediatrics +17

Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene

Guadalupe Maya‐Núñez, Sergio A. Cuevas‐Covarrubias, Juan Carlos Zenteno et al. · Clinical Endocrinology · 1998 · 39 citations

Life Sciences, Endocrinology, Genetics +17

Deletion Pattern of the STS Gene in X-linked Ichthyosis in a Mexican Population

Ana Luisa Jimenez Vaca, Margarita Valdés‐Flores, María del Refugio Rivera‐Vega et al. · Molecular Medicine · 2001 · 33 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Whole sequence of the mitochondrial DNA genome of Kearns Sayre Syndrome patients: Identification of deletions and variants

Angélica Saldaña‐Martínez, Marı́a de Lourdes Muñoz, Gerardo Pérez‐Ramírez et al. · Gene · 2018 · 24 citations

Life Sciences, Genetics, Molecular Genetics +16