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.
Citación estilo ChicagoTan, Li, Bo Bi, Peiwei Zhao, Xiaonan Cai, Chunhui Wan, Jianbo Shao, and Xuelian He. "Severe Congenital Microcephaly With 16p13.11 Microdeletion Combined With NDE1 Mutation, a Case Report and Literature Review." BMC Med Genet 2017.
Cita MLATan, Li, et al. "Severe Congenital Microcephaly With 16p13.11 Microdeletion Combined With NDE1 Mutation, a Case Report and Literature Review." BMC Med Genet 2017.
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