APA引文

Rolvien, T., Kornak, U., Linke, S. J., Amling, M., & Oheim, R. (2020). Whole-Exome Sequencing Identifies Novel Compound Heterozygous ZNF469 Mutations in Two Siblings with Mild Brittle Cornea Syndrome. Calcif Tissue Int.

Citação norma Chicago

Rolvien, Tim, Uwe Kornak, Stephan J. Linke, Michael Amling, and Ralf Oheim. "Whole-Exome Sequencing Identifies Novel Compound Heterozygous ZNF469 Mutations in Two Siblings With Mild Brittle Cornea Syndrome." Calcif Tissue Int 2020.

MLA引文

Rolvien, Tim, et al. "Whole-Exome Sequencing Identifies Novel Compound Heterozygous ZNF469 Mutations in Two Siblings With Mild Brittle Cornea Syndrome." Calcif Tissue Int 2020.