Tan, L., Bi, B., Zhao, P., Cai, X., Wan, C., Shao, J., & He, X. (2017). Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review. BMC Med Genet.
استشهاد بنمط شيكاغوTan, Li, Bo Bi, Peiwei Zhao, Xiaonan Cai, Chunhui Wan, Jianbo Shao, و Xuelian He. "Severe Congenital Microcephaly With 16p13.11 Microdeletion Combined With NDE1 Mutation, a Case Report and Literature Review." BMC Med Genet 2017.
MLA استشهادTan, Li, et al. "Severe Congenital Microcephaly With 16p13.11 Microdeletion Combined With NDE1 Mutation, a Case Report and Literature Review." BMC Med Genet 2017.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.