APA (7th ed.) Citation

Chih-Ping Chen, Ming-Huei Lin, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, . . . Wayseen Wang. (2021). Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome. Elsevier.

Chicago Style (17th ed.) Citation

Chih-Ping Chen, et al. Prenatal Diagnosis of a 15q11.2-q14 Deletion of Paternal Origin Associated with Increased Nuchal Translucency, Mosaicism for De Novo Multiple Unbalanced Translocations Involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi Syndrome. Elsevier, 2021.

MLA (9th ed.) Citation

Chih-Ping Chen, et al. Prenatal Diagnosis of a 15q11.2-q14 Deletion of Paternal Origin Associated with Increased Nuchal Translucency, Mosaicism for De Novo Multiple Unbalanced Translocations Involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi Syndrome. Elsevier, 2021.