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Case Reports

Short-rib polydactyly syndrome presenting with recurrent severe first-trimester phenotypes: the utility of exome sequencing in deciphering variants of DYNC2H1 gene

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Pages 874-876 | Published online: 14 Oct 2019
 

Disclosure statement

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the article.

Additional information

Funding

This study was supported by a grant from the Guangzhou Institute of Pediatrics/Guangzhou Women and Children’s Medical Center [IP-2019-004].

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