Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation.

MLA

Wang, Xue, et al. “Exome Sequencing Reveals a Heterozygous DLX5 Mutation in a Chinese Family with Autosomal-Dominant Split-Hand/Foot Malformation.” European Journal of Human Genetics, vol. 22, no. 9, Sept. 2014, pp. 1105–10. EBSCOhost, https://doi.org/10.1038/ejhg.2014.7.

APA

Wang, X., Xin, Q., Li, L., Li, J., Zhang, C., Qiu, R., Qian, C., Zhao, H., Liu, Y., Shan, S., Dang, J., Bian, X., Shao, C., Gong, Y., & Liu, Q. (2014). Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation. European Journal of Human Genetics, 22(9), 1105–1110. https://doi.org/10.1038/ejhg.2014.7

Chicago

Wang, Xue, Qian Xin, Lin Li, Jiangxia Li, Changwu Zhang, Rongfang Qiu, Chenmin Qian, et al. 2014. “Exome Sequencing Reveals a Heterozygous DLX5 Mutation in a Chinese Family with Autosomal-Dominant Split-Hand/Foot Malformation.” European Journal of Human Genetics 22 (9): 1105–10. doi:10.1038/ejhg.2014.7.