APA استشهاد

Habib, A., Shojazadeh, A., Molayemat, M., Jafari Khamirani, H., Zoghi, S., Dastgheib, S. A., & Habib, A. (2021). A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation site. Hum Genome Var.

استشهاد بنمط شيكاغو

Habib, Ashkan, Alireza Shojazadeh, Mohadeseh Molayemat, Hossein Jafari Khamirani, Sina Zoghi, Seyed Alireza Dastgheib, و Asadollah Habib. "A Single-amino-acid In-frame Deletion in CYP17A1 Results in Combined 17-hydroxylase and 17,20-lyase Deficiency in an Iranian Family Despite the Protein Mutation Site." Hum Genome Var 2021.

MLA استشهاد

Habib, Ashkan, et al. "A Single-amino-acid In-frame Deletion in CYP17A1 Results in Combined 17-hydroxylase and 17,20-lyase Deficiency in an Iranian Family Despite the Protein Mutation Site." Hum Genome Var 2021.

تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.