TUNCER KILINÇ, F. N. Et Al. 2016. A novel mutation in PCDH19 enabled genetic diagnosis as Epilepsy and Mental Retardation Limited to Females. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.24 , 192.

TUNCER KILINÇ, F. N. , UĞUR İŞERİ, S. A. , Kara, B., Maraş Genç, H., Uyur Yalçın, E., & ÖZBEK, U., (2016). A novel mutation in PCDH19 enabled genetic diagnosis as Epilepsy and Mental Retardation Limited to Females. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.24, 192.

TUNCER KILINÇ, Feyza Et Al. "A novel mutation in PCDH19 enabled genetic diagnosis as Epilepsy and Mental Retardation Limited to Females," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.24, 192, 2016

TUNCER KILINÇ, Feyza N. Et Al. "A novel mutation in PCDH19 enabled genetic diagnosis as Epilepsy and Mental Retardation Limited to Females." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.24, pp.192, 2016

TUNCER KILINÇ, F. N. Et Al. (2016) . "A novel mutation in PCDH19 enabled genetic diagnosis as Epilepsy and Mental Retardation Limited to Females." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.24, p.192.

@article{article, author={Feyza Nur TUNCER KILINÇ Et Al. }, title={A novel mutation in PCDH19 enabled genetic diagnosis as Epilepsy and Mental Retardation Limited to Females}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2016, pages={192} }