APA引文

Ramzan, K., Al-Numair, N. S., Al-Ageel, S., Elbaik, L., Sakati, N., Al-Hazzaa, S. A. F., . . . Imtiaz, F. (2020). Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss. Genes (Basel).

Citação norma Chicago

Ramzan, Khushnooda, Nouf S. Al-Numair, Sarah Al-Ageel, Lina Elbaik, Nadia Sakati, Selwa A. F. Al-Hazzaa, Mohammed Al-Owain, and Faiqa Imtiaz. "Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss." Genes (Basel) 2020.

MLA引文

Ramzan, Khushnooda, et al. "Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss." Genes (Basel) 2020.