Ay, B. Et Al. 2024. CFAP99 deficiency leads to heterotaxy and scoliosis. EUROPEAN JOURNAL OF HUMAN GENETICS , 1747-1748.

Ay, B., Viviano, S., AKGÜN DOĞAN, Ö., ALANAY, Y., & Deniz, E., (2024). CFAP99 deficiency leads to heterotaxy and scoliosis. EUROPEAN JOURNAL OF HUMAN GENETICS , 1747-1748.

Ay, Beril Et Al. "CFAP99 deficiency leads to heterotaxy and scoliosis," EUROPEAN JOURNAL OF HUMAN GENETICS , 1747-1748, 2024

Ay, Beril Et Al. "CFAP99 deficiency leads to heterotaxy and scoliosis." EUROPEAN JOURNAL OF HUMAN GENETICS , pp.1747-1748, 2024

Ay, B. Et Al. (2024) . "CFAP99 deficiency leads to heterotaxy and scoliosis." EUROPEAN JOURNAL OF HUMAN GENETICS , pp.1747-1748.

@article{article, author={Beril Ay Et Al. }, title={CFAP99 deficiency leads to heterotaxy and scoliosis}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2024, pages={1747-1748} }