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

Advances in oto-rhino-laryngology

Volumn 56, Issue , 2000, Pages 158-163

  Scott, H S ^a   Antonarakis, S E ^a   Mittaz, L ^a   Lalioti, M D ^a   Younus, F ^a   Mohyuddin, A ^a   Mehdi, S Q ^a   Gal, A ^a  

^a UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 21; CHROMOSOME MAP; FEMALE; GENETICS; HEARING IMPAIRMENT; HUMAN; MALE; PEDIGREE; RECESSIVE GENE; REVIEW;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 21; DEAFNESS; FEMALE; GENES, RECESSIVE; HUMANS; MALE; PEDIGREE;

MLCS; MLOWN;

EID: 0033656865     PISSN: 00653071     EISSN: None     Source Type: Journal    
DOI: 10.1159/000059096     Document Type: Review

References (23)