APA

Chen C., Lin C., Chen Y., Wang L., Chern S., Wu P., Su J., Chen L., Town D., Pan C. & Wang W. (20131223). 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization. : Gene.

Chicago

Chen Chih-Ping, Lin Chen-Ju, Chen Yi-Yung, Wang Liang-Kai, Chern Schu-Rern, Wu Peih-Shan, Su Jun-Wei, Chen Li-Feng, Town Dai-Dyi, Pan Chen-Wen and Wang Wayseen. 20131223. 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization. : Gene.

Harvard

Chen C., Lin C., Chen Y., Wang L., Chern S., Wu P., Su J., Chen L., Town D., Pan C. and Wang W. (20131223). 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization. : Gene.

MLA

Chen Chih-Ping, Lin Chen-Ju, Chen Yi-Yung, Wang Liang-Kai, Chern Schu-Rern, Wu Peih-Shan, Su Jun-Wei, Chen Li-Feng, Town Dai-Dyi, Pan Chen-Wen and Wang Wayseen. 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization. : Gene. 20131223.