NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

MLA

David A. Piccoli, et al. “NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway.” The American Journal of Human Genetics, vol. 79, no. 1, July 2006, pp. 169–73. EBSCOhost, https://doi.org/10.1086/505332.

APA

David A. Piccoli, Ryan McDaniell, Pedro A. Sanchez-Lara, Ian D. Krantz, Nancy B. Spinner, Daniel M. Warthen, & Athma A. Pai. (2006). NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway. The American Journal of Human Genetics, 79(1), 169–173. https://doi.org/10.1086/505332

Chicago

David A. Piccoli, Ryan McDaniell, Pedro A. Sanchez-Lara, Ian D. Krantz, Nancy B. Spinner, Daniel M. Warthen, and Athma A. Pai. 2006. “NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway.” The American Journal of Human Genetics 79 (1): 169–73. doi:10.1086/505332.