APA

Tsai E. A., Grochowski C. M., Falsey A. M., Rajagopalan R., Wendel D., Devoto M., Krantz I. D., Loomes K. M. & Spinner N. B. (20160301). Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia. : Human mutation.

Chicago

Tsai Ellen A, Grochowski Christopher M, Falsey Alexandra M, Rajagopalan Ramakrishnan, Wendel Danielle, Devoto Marcella, Krantz Ian D, Loomes Kathleen M and Spinner Nancy B. 20160301. Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia. : Human mutation.

Harvard

Tsai E. A., Grochowski C. M., Falsey A. M., Rajagopalan R., Wendel D., Devoto M., Krantz I. D., Loomes K. M. and Spinner N. B. (20160301). Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia. : Human mutation.

MLA

Tsai Ellen A, Grochowski Christopher M, Falsey Alexandra M, Rajagopalan Ramakrishnan, Wendel Danielle, Devoto Marcella, Krantz Ian D, Loomes Kathleen M and Spinner Nancy B. Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia. : Human mutation. 20160301.