APA

Guo X., Song C., Shi Y., Li H., Meng W., Yuan Q., Xue J., Xie J., Liang Y., Yuan Y., Yu B., Wang H., Chen Y., Qi L. & Li X. (20170515). Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly. : BMC medical genetics.

Chicago

Guo Xingping, Song Chunying, Shi Yaping, Li Hongxia, Meng Weijing, Yuan Qinzhao, Xue Jinjie, Xie Jun, Liang Yunxia, Yuan Yanan, Yu Baofeng, Wang Huaixiu, Chen Yun, Qi Lixin and Li Xinmin. 20170515. Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly. : BMC medical genetics.

Harvard

Guo X., Song C., Shi Y., Li H., Meng W., Yuan Q., Xue J., Xie J., Liang Y., Yuan Y., Yu B., Wang H., Chen Y., Qi L. and Li X. (20170515). Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly. : BMC medical genetics.

MLA

Guo Xingping, Song Chunying, Shi Yaping, Li Hongxia, Meng Weijing, Yuan Qinzhao, Xue Jinjie, Xie Jun, Liang Yunxia, Yuan Yanan, Yu Baofeng, Wang Huaixiu, Chen Yun, Qi Lixin and Li Xinmin. Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly. : BMC medical genetics. 20170515.