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