APA Цитирование

Haraksingh, R. R., Jahanbani, F., Rodriguez-Paris, J., Gelernter, J., Nadeau, K. C., Oghalai, J. S., . . . Snyder, M. P. (2014). Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss. BMC Genomics.

Chicago-стиль цитирования

Haraksingh, Rajini R., Fereshteh Jahanbani, Juan Rodriguez-Paris, Joel Gelernter, Kari C. Nadeau, John S. Oghalai, Iris Schrijver, and Michael P. Snyder. "Exome Sequencing and Genome-wide Copy Number Variant Mapping Reveal Novel Associations With Sensorineural Hereditary Hearing Loss." BMC Genomics 2014.

MLA-цитирование

Haraksingh, Rajini R., et al. "Exome Sequencing and Genome-wide Copy Number Variant Mapping Reveal Novel Associations With Sensorineural Hereditary Hearing Loss." BMC Genomics 2014.

Предупреждение: эти цитированмия не могут быть всегда правильны на 100%.