Deng, H., Lu, Q., Xu, H., Deng, X., Yuan, L., Yang, Z., . . . Song, Z. (2016). Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing. PLoS One.
Citação norma ChicagoDeng, Hao, et al. "Identification of a Novel Missense FBN2 Mutation in a Chinese Family With Congenital Contractural Arachnodactyly Using Exome Sequencing." PLoS One 2016.
Citação norma MLADeng, Hao, et al. "Identification of a Novel Missense FBN2 Mutation in a Chinese Family With Congenital Contractural Arachnodactyly Using Exome Sequencing." PLoS One 2016.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.