Cita APA

Ercan-Sencicek, A. G., Jambi, S., Franjic, D., Nishimura, S., Li, M., El-Fishawy, P., . . . State, M. W. (2015). Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. Eur J Hum Genet.

Chicago Style Citation

Ercan-Sencicek, A Gulhan, et al. "Homozygous Loss of DIAPH1 Is a Novel Cause of Microcephaly in Humans." Eur J Hum Genet 2015.

Cita MLA

Ercan-Sencicek, A Gulhan, et al. "Homozygous Loss of DIAPH1 Is a Novel Cause of Microcephaly in Humans." Eur J Hum Genet 2015.