Araceli Álvarez

RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections

E. Zackai, E. Bermejo, B. Weschke, 2003, Journal of medical genetics.

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.

F. Moreno, D. Tellería, I. del Castillo, 2002, The New England journal of medicine.

A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

A. Pandya, C. Petit, D. Weil, 2005, Journal of Medical Genetics.

High prevalence of the W24X mutation in the gene encoding connexin‐26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non‐syndromic hearing loss

A. González-Neira, F. Moreno, I. del Castillo, 2005, American journal of medical genetics. Part A.

Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study.

X. Estivill, A. Pandya, C. Petit, 2003, American journal of human genetics.

De novo mutation in the gene encoding connexin‐26 (GJB2) in a sporadic case of keratitis‐ichthyosis‐deafness (KID) syndrome

F. Moreno, A. Pera, I. del Castillo, 2003, American journal of medical genetics. Part A.