A novel autosomal dominant mutation in SOX18 resulting in a fatal case of hypotrichosis-lymphedema-telangiectasia syndrome.

MLA

Wangberg, Hannah, et al. “A Novel Autosomal Dominant Mutation in SOX18 Resulting in a Fatal Case of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.” American Journal of Medical Genetics. Part A, vol. 176, no. 12, Dec. 2018, pp. 2824–28. EBSCOhost, https://doi.org/10.1002/ajmg.a.40532.

APA

Wangberg, H., Wigby, K., & Jones, M. C. (2018). A novel autosomal dominant mutation in SOX18 resulting in a fatal case of hypotrichosis-lymphedema-telangiectasia syndrome. American Journal of Medical Genetics. Part A, 176(12), 2824–2828. https://doi.org/10.1002/ajmg.a.40532

Chicago

Wangberg, Hannah, Kristen Wigby, and Marilyn C Jones. 2018. “A Novel Autosomal Dominant Mutation in SOX18 Resulting in a Fatal Case of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.” American Journal of Medical Genetics. Part A 176 (12): 2824–28. doi:10.1002/ajmg.a.40532.