Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders

MLA

Brent L. Fogel, et al. “Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders.” JAMA, vol. 312, Nov. 2014, p. 1880. EBSCOhost, https://doi.org/10.1001/jama.2014.14604.

APA

Brent L. Fogel, Stanley F. Nelson, Sibel Kantarci, Traci Toy, Samuel P. Strom, Kingshuk Das, Perry B. Shieh, Christina G.S. Palmer, Hane Lee, Fabiola Quintero-Rivera, Derek Wong, Michelle Fox, Vivian Y. Chang, Joshua L. Deignan, Wayne W. Grody, Katrina M. Dipple, Michael Yourshaw, Naghmeh Dorrani, Julian A. Martinez-Agosto, … Eric Vilain. (2014). Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders. JAMA, 312, 1880. https://doi.org/10.1001/jama.2014.14604

Chicago

Brent L. Fogel, Stanley F. Nelson, Sibel Kantarci, Traci Toy, Samuel P. Strom, Kingshuk Das, Perry B. Shieh, et al. 2014. “Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders.” JAMA 312 (November): 1880. doi:10.1001/jama.2014.14604.