TEKİN, M. N. Et Al. 2008. Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia. CLINICAL GENETICS , vol.73, no.6 , 554-565.

TEKİN, M. N., Akay, H. O., Fitoz, S., Birnbaum, S., Cengiz, F. B., SENNAROĞLU, L., ... İNCESULU, Ş. A.(2008). Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia. CLINICAL GENETICS , vol.73, no.6, 554-565.

TEKİN, MERVE Et Al. "Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia," CLINICAL GENETICS , vol.73, no.6, 554-565, 2008

TEKİN, MERVE N. Et Al. "Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia." CLINICAL GENETICS , vol.73, no.6, pp.554-565, 2008

TEKİN, M. N. Et Al. (2008) . "Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia." CLINICAL GENETICS , vol.73, no.6, pp.554-565.

@article{article, author={MERVE NUR TEKİN Et Al. }, title={Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia}, journal={CLINICAL GENETICS}, year=2008, pages={554-565} }