APA

Sung P., Chang C., Chen C., Wang P., Chao K., Wen K., Cheng Y., Li Y. & Lin C. (20130131). Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly. : Taiwanese journal of obstetrics & gynecology.

Chicago

Sung Pi-Lin, Chang Chia-Ming, Chen Chih-Yao, Wang Peng-Hui, Chao Kuan-Chong, Wen Kuo-Chang, Cheng Yung-Yung, Li Yueh-Chun and Lin Chyi-Chyang. 20130131. Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly. : Taiwanese journal of obstetrics & gynecology.

Harvard

Sung P., Chang C., Chen C., Wang P., Chao K., Wen K., Cheng Y., Li Y. and Lin C. (20130131). Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly. : Taiwanese journal of obstetrics & gynecology.

MLA

Sung Pi-Lin, Chang Chia-Ming, Chen Chih-Yao, Wang Peng-Hui, Chao Kuan-Chong, Wen Kuo-Chang, Cheng Yung-Yung, Li Yueh-Chun and Lin Chyi-Chyang. Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly. : Taiwanese journal of obstetrics & gynecology. 20130131.