Cita APA (7a ed.)
Nasrniya, S., Miar, P., Narrei, S., Sepehrnejad, M., Nilforoush, M. H., Abtahi, H., & Tabatabaiefar, M. A. (2022). Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees. Laboratory Medicine, 53(2), 111-123.
Cita Chicago Style (17a ed.)
Nasrniya, Samane, Paniz Miar, Sina Narrei, Mahsa Sepehrnejad, Mohammad Hussein Nilforoush, Hamidreza Abtahi, y Mohammad Amin Tabatabaiefar. "Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees." Laboratory Medicine 53, no. 2 (2022): 111-123.
Cita MLA (9a ed.)
Nasrniya, Samane, et al. "Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees." Laboratory Medicine, vol. 53, no. 2, 2022, pp. 111-123.
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