E. Kalay Et Al. , "Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss," HUMAN MUTATION , vol.27, no.7, pp.633-639, 2006
Kalay, E. Et Al. 2006. Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss. HUMAN MUTATION , vol.27, no.7 , 633-639.
Kalay, E., Li, Y., Uzumcu, A., Uyguner, O., Collin, R. W., Caylan, R., ... Ulubil-Emiroglu, M.(2006). Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss. HUMAN MUTATION , vol.27, no.7, 633-639.
Kalay, Ersan Et Al. "Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss," HUMAN MUTATION , vol.27, no.7, 633-639, 2006
Kalay, Ersan Et Al. "Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss." HUMAN MUTATION , vol.27, no.7, pp.633-639, 2006
Kalay, E. Et Al. (2006) . "Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss." HUMAN MUTATION , vol.27, no.7, pp.633-639.
@article{article, author={Ersan Kalay Et Al. }, title={Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss}, journal={HUMAN MUTATION}, year=2006, pages={633-639} }