APA (7th ed.) Citation

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, . . . Wayseen Wang. (2016). Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot. Elsevier.

Chicago Style (17th ed.) Citation

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Li-Feng Chen, Chien-Wen Yang, and Wayseen Wang. Prenatal Diagnosis and Molecular Cytogenetic Characterization of a De Novo 4.858-Mb Microdeletion in 15q14 Associated with ACTC1 and MEIS2 Haploinsufficiency and Tetralogy of Fallot. Elsevier, 2016.

MLA (9th ed.) Citation

Chih-Ping Chen, et al. Prenatal Diagnosis and Molecular Cytogenetic Characterization of a De Novo 4.858-Mb Microdeletion in 15q14 Associated with ACTC1 and MEIS2 Haploinsufficiency and Tetralogy of Fallot. Elsevier, 2016.