Dyfyniad APA

Geng, K., Mu, K., Zhao, Y., Luan, J., Cui, Y., & Han, J. (2020). Identification of novel compound heterozygous mutations of the DYNC2H1 gene in a fetus with short-rib thoracic dysplasia 3 with or without polydactyly. Intractable Rare Dis Res.

Dyfyniad Arddull Chicago

Geng, Kaiyue, Kai Mu, Yan Zhao, Jing Luan, Yazhou Cui, and Jinxiang Han. "Identification of Novel Compound Heterozygous Mutations of the DYNC2H1 Gene in a Fetus With Short-rib Thoracic Dysplasia 3 With or Without Polydactyly." Intractable Rare Dis Res 2020.

Dyfyniad MLA

Geng, Kaiyue, et al. "Identification of Novel Compound Heterozygous Mutations of the DYNC2H1 Gene in a Fetus With Short-rib Thoracic Dysplasia 3 With or Without Polydactyly." Intractable Rare Dis Res 2020.

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