A. Topf Et Al. , "Severe neurodevelopmental disease caused by a homozygous TLK2 variant," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.3, pp.383-387, 2020
Topf, A. Et Al. 2020. Severe neurodevelopmental disease caused by a homozygous TLK2 variant. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.3 , 383-387.
Topf, A., OKTAY, Y., Balaraju, S., Yilmaz, E., Sonmezler, E., YİŞ, U., ... Laurie, S.(2020). Severe neurodevelopmental disease caused by a homozygous TLK2 variant. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.3, 383-387.
Topf, Ana Et Al. "Severe neurodevelopmental disease caused by a homozygous TLK2 variant," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.3, 383-387, 2020
Topf, Ana Et Al. "Severe neurodevelopmental disease caused by a homozygous TLK2 variant." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.3, pp.383-387, 2020
Topf, A. Et Al. (2020) . "Severe neurodevelopmental disease caused by a homozygous TLK2 variant." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.3, pp.383-387.
@article{article, author={Ana Topf Et Al. }, title={Severe neurodevelopmental disease caused by a homozygous TLK2 variant}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2020, pages={383-387} }