Türkyılmaz, A. Et Al. 2024. A triple molecular diagnosis in a Turkish individual with hypotrichosis, deafness, and diabetes. CLINICAL DYSMORPHOLOGY , vol.33, no.3 , 118-120.

Türkyılmaz, A., Cimbek, E. A., Kardeş, H., Çebi, A. H., Acar Arslan, E., & Karagüzel, G., (2024). A triple molecular diagnosis in a Turkish individual with hypotrichosis, deafness, and diabetes. CLINICAL DYSMORPHOLOGY , vol.33, no.3, 118-120.

Türkyılmaz, AYBERK Et Al. "A triple molecular diagnosis in a Turkish individual with hypotrichosis, deafness, and diabetes," CLINICAL DYSMORPHOLOGY , vol.33, no.3, 118-120, 2024

Türkyılmaz, AYBERK Et Al. "A triple molecular diagnosis in a Turkish individual with hypotrichosis, deafness, and diabetes." CLINICAL DYSMORPHOLOGY , vol.33, no.3, pp.118-120, 2024

Türkyılmaz, A. Et Al. (2024) . "A triple molecular diagnosis in a Turkish individual with hypotrichosis, deafness, and diabetes." CLINICAL DYSMORPHOLOGY , vol.33, no.3, pp.118-120.

@article{article, author={AYBERK TÜRKYILMAZ Et Al. }, title={A triple molecular diagnosis in a Turkish individual with hypotrichosis, deafness, and diabetes}, journal={CLINICAL DYSMORPHOLOGY}, year=2024, pages={118-120} }