Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3

Scott, Hamish Steele; Antonarakis, Stylianos; Mittaz, L.; Lalioti, M. D.; Younus, F.; Mohyuddin, A.; Mehdi, S. Q.; Gal, A.

doi:10.1159/000059096

Scientific article

English

Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3

ContributorsScott, Hamish Steele; Antonarakis, Stylianos; Mittaz, L.; Lalioti, M. D.; Younus, F.; Mohyuddin, A.; Mehdi, S. Q.; Gal, A.

Published inAdvances in oto-rhino-laryngology, vol. 56, p. 158-163

Publication date2000

Keywords

Chromosome Mapping
Chromosomes, Human, Pair 21
Deafness/ genetics
Female
Genes, Recessive
Humans
Male
Pedigree

Affiliation entities

Faculté de médecine / Section de médecine fondamentale / Département de médecine génétique et développement

Citation (ISO format)

SCOTT, Hamish Steele et al. Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3. In: Advances in oto-rhino-laryngology, 2000, vol. 56, p. 158–163. doi: 10.1159/000059096

Identifiers

PID : unige:9259
DOI : 10.1159/000059096
PMID : 10868228

Journal ISSN0065-3071

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Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3

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