Özmen, Meral

Istanbul University

1 paper on CoChatORCID 0000-0003-4316-1499

Most cited papers

Verified
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
Bilgüvar, K., Öztürk, A. K., Louvi, A., Kwan, K. Y., Choi, M., Tatlı, B., Yalnızoğlu, D., Tüysüz, B., Çağlayan, A. O., Gökben, S., et al. (2010) · Nature
Fetal and Pediatric Neurological DisordersGenetics and Neurodevelopmental Disorders
Cited by 503

Go further with a free account

Verify every reference, keep papers in a library, and ask questions across them.

Sign up - it is free