APA (7th ed.) Citation

Netravathi, M., Kumari, R., Kapoor, S., Dakle, P., Dwivedi, M. K., Roy, S. D., . . . Faruq, M. (2015). Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. BMC Medical Genetics, 16(1), 1. https://doi.org/10.1186/s12881-015-0151-8

Chicago Style (17th ed.) Citation

Netravathi, Manjunath, et al. "Whole Exome Sequencing in an Indian Family Links Coats Plus Syndrome and Dextrocardia with a Homozygous Novel CTC1 and a Rare HES7 Variation." BMC Medical Genetics 16, no. 1 (2015): 1. https://doi.org/10.1186/s12881-015-0151-8.

MLA (9th ed.) Citation

Netravathi, Manjunath, et al. "Whole Exome Sequencing in an Indian Family Links Coats Plus Syndrome and Dextrocardia with a Homozygous Novel CTC1 and a Rare HES7 Variation." BMC Medical Genetics, vol. 16, no. 1, 2015, p. 1, https://doi.org/10.1186/s12881-015-0151-8.