Cita APA (7a ed.)

Mohammadi, P., Siavashani, E. S., Mohammadi, M. F., Bahramy, A., Almadani, N., & Garshasbi, M. (2021). Whole‐exome sequencing identified first homozygous frameshift variant in the COLEC10 gene in an Iranian patient causing 3MC syndrome type 3. Wiley.

Cita Chicago Style (17a ed.)

Mohammadi, Pouria, Elham Salehi Siavashani, Mohammad Farid Mohammadi, Afshin Bahramy, Navid Almadani, y Masoud Garshasbi. Whole‐exome Sequencing Identified First Homozygous Frameshift Variant in the COLEC10 Gene in an Iranian Patient Causing 3MC Syndrome Type 3. Wiley, 2021.

Cita MLA (8a ed.)

Mohammadi, Pouria, et al. Whole‐exome Sequencing Identified First Homozygous Frameshift Variant in the COLEC10 Gene in an Iranian Patient Causing 3MC Syndrome Type 3. Wiley, 2021.