APA (7th ed.) Citation

AE, L., C, M., V, C., TJ, L., GP, M., BH, B., . . . ME, L. (2016). Gain-of-function mutations in SMAD4 cause a distinctive repertoire of cardiovascular phenotypes in patients with Myhre syndrome. American journal of medical genetics. Part A, 170(10), 2617. https://doi.org/10.1002/ajmg.a.37739

Chicago Style (17th ed.) Citation

AE, Lin, et al. "Gain-of-function Mutations in SMAD4 Cause a Distinctive Repertoire of Cardiovascular Phenotypes in Patients with Myhre Syndrome." American Journal of Medical Genetics. Part A 170, no. 10 (2016): 2617. https://doi.org/10.1002/ajmg.a.37739.

MLA (9th ed.) Citation

AE, Lin, et al. "Gain-of-function Mutations in SMAD4 Cause a Distinctive Repertoire of Cardiovascular Phenotypes in Patients with Myhre Syndrome." American Journal of Medical Genetics. Part A, vol. 170, no. 10, 2016, p. 2617, https://doi.org/10.1002/ajmg.a.37739.