Yalnızoğlu, Dilek

Hacettepe University

1 paper on CoChatORCID 0000-0001-9294-4305

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

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