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, pp.633-9, 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 , 633-9.
Kalay, E., Li, Y., Üzümcü, A., UYGUNER, Z. O., Karagüzel, a., Becker, C., ... Cremers, C.(2006). Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.. HUMAN MUTATION , vol.27, 633-9.
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, 633-9, 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, pp.633-9, 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, pp.633-9.
@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={633-9} }