Cita APA

Guo, X., Song, C., Shi, Y., Li, H., Meng, W., Yuan, Q., . . . Li, X. (2016). Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly. BMC Med Genet.

Chicago Style Citation

Guo, Xingping, et al. "Whole Exome Sequencing Identifies a Novel Missense FBN2 Mutation Co-segregating in a Four-generation Chinese Family With Congenital Contractural Arachnodactyly." BMC Med Genet 2016.

Cita MLA

Guo, Xingping, et al. "Whole Exome Sequencing Identifies a Novel Missense FBN2 Mutation Co-segregating in a Four-generation Chinese Family With Congenital Contractural Arachnodactyly." BMC Med Genet 2016.