Dyfyniad APA

Zhang, L., Fu, S., Ou, Y., Zhao, T., Su, Y., & Liu, P. (2009). A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea. Molecular Vision.

Dyfyniad Arddull Chicago

Zhang, Lu, Songbin Fu, Yangshan Ou, Tingting Zhao, Yunjuan Su, and Ping Liu. A Novel Nonsense Mutation in CRYGC Is Associated With Autosomal Dominant Congenital Nuclear Cataracts and Microcornea. Molecular Vision, 2009.

Dyfyniad MLA

Zhang, Lu, et al. A Novel Nonsense Mutation in CRYGC Is Associated With Autosomal Dominant Congenital Nuclear Cataracts and Microcornea. Molecular Vision, 2009.

Rhybudd: Mae'n bosib nad yw'r dyfyniadau hyn bob amser yn 100% cywir.