Yilmaz, B. Et Al. 2017. Familial occurrence of brain arteriovenous malformation: a novel ACVRL1 mutation detected by whole exome sequencing. JOURNAL OF NEUROSURGERY , vol.126, no.6 , 1879-1883.

Yilmaz, B., Toktas, Z. O., Akakin, A., Isik, S., Bilguvar, K., Kilic, T., ... Gunel, M.(2017). Familial occurrence of brain arteriovenous malformation: a novel ACVRL1 mutation detected by whole exome sequencing. JOURNAL OF NEUROSURGERY , vol.126, no.6, 1879-1883.

Yilmaz, Baran Et Al. "Familial occurrence of brain arteriovenous malformation: a novel ACVRL1 mutation detected by whole exome sequencing," JOURNAL OF NEUROSURGERY , vol.126, no.6, 1879-1883, 2017

Yilmaz, Baran Et Al. "Familial occurrence of brain arteriovenous malformation: a novel ACVRL1 mutation detected by whole exome sequencing." JOURNAL OF NEUROSURGERY , vol.126, no.6, pp.1879-1883, 2017

Yilmaz, B. Et Al. (2017) . "Familial occurrence of brain arteriovenous malformation: a novel ACVRL1 mutation detected by whole exome sequencing." JOURNAL OF NEUROSURGERY , vol.126, no.6, pp.1879-1883.

@article{article, author={Baran Yilmaz Et Al. }, title={Familial occurrence of brain arteriovenous malformation: a novel ACVRL1 mutation detected by whole exome sequencing}, journal={JOURNAL OF NEUROSURGERY}, year=2017, pages={1879-1883} }