15 results on '"Pelayo, M."'
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2. Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C→T mutation in the mitochondrial 12S rRNA gene
3. 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
4. A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci
5. DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23
6. Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss
7. Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients
8. Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNASer(UCN) gene
9. Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss
10. Complete cDNA sequence of the HLA-DRB1*09012 allele*
11. Polymorphism of Mhc-DRB alleles in Cercopithecus aethiops (green monkey): generation and functionality
12. DESCRIPTION OF A NEW HLA-DRB3 ALLELE: HLA-DRB3*01012
13. COMPLETE NUCLEOTIDE SEQUENCE OF THE HLA-DRB1*1302 ALLELE
14. DESCRIPTION OF A NEW HLA-DRB1 ALLELE: HLA-DRB1*0310
15. Description of two new HLA-DRB alleles (DRB1*0310 and DRB3*01012) found in a Spanish infant
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