A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

D A Campbell; D P McHale; K A Brown; L M Moynihan; M Houseman; G Karbani; G Parry; A H Janjua; V Newton; L al-Gazali; A F Markham; N J Lench; R F Mueller

doi:10.1136/jmg.34.12.1015

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Research Article

A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

Authors

D A Campbell PubMed articles Google scholar articles
D P McHale PubMed articles Google scholar articles
K A Brown PubMed articles Google scholar articles
L M Moynihan PubMed articles Google scholar articles
M Houseman PubMed articles Google scholar articles
G Karbani PubMed articles Google scholar articles
G Parry PubMed articles Google scholar articles
A H Janjua PubMed articles Google scholar articles
V Newton PubMed articles Google scholar articles
L al-Gazali PubMed articles Google scholar articles
A F Markham PubMed articles Google scholar articles
N J Lench PubMed articles Google scholar articles
R F Mueller PubMed articles Google scholar articles

Citation

Campbell DA, McHale DP, Brown KA, et al

A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

Journal of Medical Genetics 1997;34:1015-1017.

Publication history

First published December 1, 1997.

Online issue publication

January 04, 2017

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