Cita APA

Türkyılmaz, A., & Yaralı, O. (2020). A Very Rare Partial Trisomy Syndrome: De Novo Duplication of 16q12.1q23.3 in a Turkish Girl with Developmental Delay and Facial Dysmorphic Features. Balkan J Med Genet.

Chicago Style Citation

Türkyılmaz, A., i O. Yaralı. "A Very Rare Partial Trisomy Syndrome: De Novo Duplication of 16q12.1q23.3 in a Turkish Girl With Developmental Delay and Facial Dysmorphic Features." Balkan J Med Genet 2020.

Cita MLA

Türkyılmaz, A., i O. Yaralı. "A Very Rare Partial Trisomy Syndrome: De Novo Duplication of 16q12.1q23.3 in a Turkish Girl With Developmental Delay and Facial Dysmorphic Features." Balkan J Med Genet 2020.