Ercan-Sencicek, A. G. Et Al. 2015. Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.23, no.2 , 165-172.

Ercan-Sencicek, A. G., Jambi, S., Franjic, D., Nishimura, S., Li, M., El-Fishawy, P., ... Morgan, T. M.(2015). Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.23, no.2, 165-172.

Ercan-Sencicek, A. Et Al. "Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.23, no.2, 165-172, 2015

Ercan-Sencicek, A. G. Et Al. "Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.23, no.2, pp.165-172, 2015

Ercan-Sencicek, A. G. Et Al. (2015) . "Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.23, no.2, pp.165-172.

@article{article, author={A. Gulhan Ercan-Sencicek Et Al. }, title={Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2015, pages={165-172} }