L. Gonzalez-Huerta

Segregation analysis in X‐linked ichthyosis: paternal transmission of the affected X‐chromosome

S. Cuevas-Covarrubias, J. Toral-López, L. Gonzalez-Huerta, 2008, The British journal of dermatology.

Novel missense mutation (Arg432Cys) in a patient with steroid sulphatase‐deficiency

S. Cuevas-Covarrubias, L. Gonzalez-Huerta, M. R. Riviera‐Vega, 2003, Clinical endocrinology.

Point mutation in the STS gene in a severely affected patient with X-linked recessive ichthyosis.

S. Kofman‐Alfaro, S. Cuevas-Covarrubias, J. Toral-López, 2006, Acta dermato-venereologica.

An intellectually disabled patient with the 5q14.3q15 microdeletion syndrome associated with an apparently de novo t(2;5)(q13;q14)

J. Zenteno, B. Buentello-Volante, S. Cuevas-Covarrubias, 2012, American journal of medical genetics. Part A.

A novel microdeletion involving the 13q31.3-q32.1 region in a patient with normal intelligence.

A. Pérez-Cabrera, S. Cuevas-Covarrubias, J. Toral-López, 2014, European journal of medical genetics.

A CRYGC gene mutation associated with autosomal dominant pulverulent cataract.

S. Cuevas-Covarrubias, J. Toral-López, L. González-Huerta, 2013, Gene.

Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q

A. Pérez-Cabrera, S. Cuevas-Covarrubias, J. M. Valdes-Miranda, 2016, Cytogenetic and Genome Research.