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Prenatal diagnosis of congenital chloride diarrhea by whole exome sequencing in four Chinese families and prenatal genotype–phenotype association study

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Data availability

The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.

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Acknowledgements

We are grateful to the family members of the patients for their cooperation.

Funding

This study was funded by the National Natural Science Foundation of China (No. 81873594).

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Authors and Affiliations

Authors

Contributions

SYF: conceptualization, data curation, writing–original draft; WH: investigation, visualization. WYX: methodology, software. SLP: funding acquisition, project administration, writing–review and editing. WS: supervision, resources, writing–review and editing.

Corresponding authors

Correspondence to Le-Ping Shao or Sai Wang.

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Conflict of interest

No financial or non-financial benefits have been received or will be received from any party related directly or indirectly to the subject of this article.

Ethical approval

This study and procedures were approved by the Ethics Committee of the Affiliated Qingdao Municipal Hospital of Qingdao University. Consent for publication Informed consent to participate in the study have been obtained from their parents of patients.

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Written consent for publication of the case details together with imaging or videos have been obtained from participants or their parents.

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Cite this article

Shao, YF., Wang, H., Wang, YX. et al. Prenatal diagnosis of congenital chloride diarrhea by whole exome sequencing in four Chinese families and prenatal genotype–phenotype association study. World J Pediatr 19, 200–207 (2023). https://doi.org/10.1007/s12519-022-00634-1

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  • DOI: https://doi.org/10.1007/s12519-022-00634-1

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