APA (7th ed.) Citation

Chih-Ping Chen, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, . . . 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. Elsevier.

Chicago Style (17th ed.) Citation

Chih-Ping Chen, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, and Wayseen Wang. 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. Elsevier, 2018.

MLA (9th ed.) Citation

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. Elsevier, 2018.