APA (7th ed.) Citation

Chih-Ping Chen, Hoi-Kin Yip, Liang-Kai Wang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, . . . Wayseen Wang. (2017). Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1. Elsevier.

Chicago Style (17th ed.) Citation

Chih-Ping Chen, Hoi-Kin Yip, Liang-Kai Wang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, and Wayseen Wang. Molecular Genetic Characterization of a Prenatally Detected 1.484-Mb Xq13.3-q21.1 Duplication Encompassing ATRX and a Literature Review of Syndromic Intellectual Disability and Congenital Abnormalities in Males with a Duplication at Xq13.3-q21.1. Elsevier, 2017.

MLA (9th ed.) Citation

Chih-Ping Chen, et al. Molecular Genetic Characterization of a Prenatally Detected 1.484-Mb Xq13.3-q21.1 Duplication Encompassing ATRX and a Literature Review of Syndromic Intellectual Disability and Congenital Abnormalities in Males with a Duplication at Xq13.3-q21.1. Elsevier, 2017.