Sezer, A. Et Al. 2020. An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28 , 895.

Sezer, A., Ogutlu, O. B. G., TÜRKYILMAZ, Z., GÜCÜYENER, K., KAYHAN, G., & PERÇİN, F. E., (2020). An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, 895.

Sezer, ABDULLAH Et Al. "An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, 895, 2020

Sezer, ABDULLAH Et Al. "An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, pp.895, 2020

Sezer, A. Et Al. (2020) . "An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, p.895.

@article{article, author={ABDULLAH SEZER Et Al. }, title={An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2020, pages={895} }