Ramzan, M. Et Al. 2023. Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss. Journal of Human Genetics , vol.68, no.10 , 657-669.

Ramzan, M., DUMAN, D., Hendricks, L. C. P., Guo, S., MUTLU, A., Kalcioglu, M. T., ... Seyhan, S.(2023). Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss. Journal of Human Genetics , vol.68, no.10, 657-669.

Ramzan, Memoona Et Al. "Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss," Journal of Human Genetics , vol.68, no.10, 657-669, 2023

Ramzan, Memoona Et Al. "Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss." Journal of Human Genetics , vol.68, no.10, pp.657-669, 2023

Ramzan, M. Et Al. (2023) . "Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss." Journal of Human Genetics , vol.68, no.10, pp.657-669.

@article{article, author={Memoona Ramzan Et Al. }, title={Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss}, journal={Journal of Human Genetics}, year=2023, pages={657-669} }