Kaygusuz, E. Et Al. 2021. A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome.. Clinical genetics , vol.100, no.4 , 486-488.

Kaygusuz, E., Khayyat, A. I. A., Abdullah, U., Budde, B. S., Asif, M., Ahmed, I., ... Makhdoom, E. U. H.(2021). A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome.. Clinical genetics , vol.100, no.4, 486-488.

Kaygusuz, EMRAH Et Al. "A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome.," Clinical genetics , vol.100, no.4, 486-488, 2021

Kaygusuz, EMRAH Et Al. "A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome.." Clinical genetics , vol.100, no.4, pp.486-488, 2021

Kaygusuz, E. Et Al. (2021) . "A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome.." Clinical genetics , vol.100, no.4, pp.486-488.

@article{article, author={EMRAH KAYGUSUZ Et Al. }, title={A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome.}, journal={Clinical genetics}, year=2021, pages={486-488} }