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Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience

Crossref DOI link: https://doi.org/10.1186/s12920-022-01423-5

Published Online: 2022-12-21

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

Authors

Liang, Bin

Yu, Donghong

Zhao, Wantong

Wang, Yan

Wu, Xiaoqing

Chen, Lingji

Lin, Na

Huang, Hailong

Xu, Liangpu
Funding

Funding for this research was provided by:

Fujian Provincial Natural Science Foundation (2020J05275)

Joints Funds for the Innovation of Science and Technology, Fujian Province (2021Y9179, 2020Y9159)

Fujian Provincial Health Technology Project (2020CXB008)
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Text and Data Mining valid from 2022-12-21

Version of Record valid from 2022-12-21
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Article History

Received: 8 July 2022

Accepted: 15 December 2022

First Online: 21 December 2022

Declarations

:

: All experiments were performed in accordance with relevant guidelines and regulations. The present study was approved by the Protection of Human Ethics Committee of Fujian Provincial Maternity and Children’s Hospital (No. 2020KY113). Written informed consent was obtained from individual or guardian participants.

: All participants provided informed consent and they agreed to publish their clinical data.

: The authors declare that they have no competing interests.

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