Araceli Álvarez

A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

Ignacio del Castillo, Manuela Villamar, Miguel A. Moreno‐Pelayo et al. · New England Journal of Medicine · 2002 · 585 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

Ignacio del Castillo, Miguel A. Moreno‐Pelayo, Francisco Castillo et al. · The American Journal of Human Genetics · 2003 · 289 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

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

Araceli Álvarez, Ignacio del Castillo, Manuela Villamar et al. · American Journal of Medical Genetics Part A · 2005 · 81 citations

Life Sciences, Genetics, Molecular Genetics +17

Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (<i>GJB2</i>) results in prelingual hearing impairment in two unrelated Spanish patients: Figure 1

Araceli Álvarez · Journal of Medical Genetics · 2003 · 52 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

A case of deaf–mutism as an expression of pure word deafness: neuroimaging and electrophysiological data

Manuel Arias, Ignacio Requena, Manfredi Ventura et al. · European Journal of Neurology · 1995 · 11 citations

Education, Neurology, Neuroscience +16