APA (7th ed.) Citation

Chih-Ping Chen, Chen-Ju Lin, Yen-Ni Chen, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, . . . Wayseen Wang. (2017). Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency. Elsevier.

Chicago Style (17th ed.) Citation

Chih-Ping Chen, Chen-Ju Lin, Yen-Ni Chen, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Li-Feng Chen, and Wayseen Wang. Molecular Genetic Characterization of a Prenatally Detected De Novo Interstitial Deletion of Chromosome 2q (2q31.1-q32.1) Encompassing HOXD13, ZNF385B and ZNF804A Associated with Syndactyly and Increased First-trimester Nuchal Translucency. Elsevier, 2017.

MLA (9th ed.) Citation

Chih-Ping Chen, et al. Molecular Genetic Characterization of a Prenatally Detected De Novo Interstitial Deletion of Chromosome 2q (2q31.1-q32.1) Encompassing HOXD13, ZNF385B and ZNF804A Associated with Syndactyly and Increased First-trimester Nuchal Translucency. Elsevier, 2017.