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Identification of potential molecular mechanism related to craniofacial dysmorphism caused by FOXI3 deficiency.

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Bibliographic Details
Title: Identification of potential molecular mechanism related to craniofacial dysmorphism caused by FOXI3 deficiency.
Authors: Xing, Xiao‐Liang1,2 (AUTHOR), Zeng, Ziqiang1,2 (AUTHOR), Wang, Yana1 (AUTHOR), Pan, Bo3 (AUTHOR) 13810855912@163.com, Huang, Xueshuang1,2 (AUTHOR) xueshuanghuang@126.com
Source: Molecular Genetics & Genomic Medicine. Mar2024, Vol. 12 Issue 3, p1-11. 11p.
Database: Academic Search Ultimate
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ISSN:23249269
DOI:10.1002/mgg3.2411