Luz María González-Huerta

Analysis of the VCX3A, VCX2 and VCX3B genes shows that VCX3A gene deletion is not sufficient to result in mental retardation in X-linked ichthyosis

S.A. Cuevas-Covarrubias, Luz María González-Huerta · British Journal of Dermatology · 2007 · 48 citations

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

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

Somatic and Germinal Mosaicism for the Steroid Sulfatase Gene Deletion in a Steroid Sulfatase Deficiency Carrier

Sergio A. Cuevas‐Covarrubias, Ana Luisa Jiménez-Vaca, Luz María González-Huerta et al. · Journal of Investigative Dermatology · 2002 · 22 citations · Full text

Genetics, Pathology, Molecular Genetics +4

A family with autosomal dominant primary congenital cataract associated with a CRYGC mutation: evidence of clinical heterogeneity.

Luz María González-Huerta, Olga Messina‐Baas, Sergio A. Cuevas‐Covarrubias · PubMed · 2007 · 22 citations