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Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review

Crossref DOI link: https://doi.org/10.1186/s12881-017-0501-9

Published Online: 2017-12-01

Published Print: 2017-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Tan, Li

Bi, Bo

Zhao, Peiwei

Cai, Xiaonan

Wan, Chunhui

Shao, Jianbo

He, Xuelian http://orcid.org/0000-0002-6275-1219
Funding

Funding for this research was provided by:

Wuhan Creative Platform of Clinical Medical Research for Neurological Diseases in Children (2014-160)

Wuhan Yellow Crane (Medicine and Healthcare) (2016-01)

Health and Family Planning Commission of Hubei Province (WJ2015MB247)

Health and Family Planning Commission of Wuhan (WX16C13)