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Investigation of the genetic and clinical features of laterality disorders in prenatal diagnosis: discovery of a novel compound heterozygous mutation in the DNAH11 gene

Crossref DOI link: https://doi.org/10.1007/s00404-024-07574-3

Published Online: 2024-06-09

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

Authors

Zhang, Simin

Wang, Jingjing

Sun, Lijuan

Han, Jijing

Xiong, Xiaowei

Xiao, Dan

Wu, Qingqing https://orcid.org/0000-0002-6836-9192
Funding

Funding for this research was provided by:

National Key Research and Development Program of China (No.2016YFC1000104)

National Natural Science Foundation of China (81971619)
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Article History

Received: 5 April 2024

Accepted: 27 May 2024

First Online: 9 June 2024

Declarations

:

: The authors declare no conflict of interest.

: Written informed consent was obtained from all subjects involved in the study.

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