Cite
Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus
MLA
Chih-Ping Chen, et al. “Prenatal Diagnosis of Short-Rib Polydactyly Syndrome Type III or Short-Rib Thoracic Dysplasia 3 with or without Polydactyly (SRTD3) Associated with Compound Heterozygous Mutations in DYNC2H1 in a Fetus.” Taiwanese Journal of Obstetrics & Gynecology, vol. 57, no. 1, Feb. 2018, pp. 123–27. EBSCOhost, https://doi.org/10.1016/j.tjog.2017.12.021.
APA
Chih-Ping Chen, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, & Wayseen Wang. (2018). Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus. Taiwanese Journal of Obstetrics & Gynecology, 57(1), 123–127. https://doi.org/10.1016/j.tjog.2017.12.021
Chicago
Chih-Ping Chen, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, and Wayseen Wang. 2018. “Prenatal Diagnosis of Short-Rib Polydactyly Syndrome Type III or Short-Rib Thoracic Dysplasia 3 with or without Polydactyly (SRTD3) Associated with Compound Heterozygous Mutations in DYNC2H1 in a Fetus.” Taiwanese Journal of Obstetrics & Gynecology 57 (1): 123–27. doi:10.1016/j.tjog.2017.12.021.