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Updated: Oct 21, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactyly

Weimin Jia1, Xiaopei Zhou1, Naiqiang Guo2

  • 1Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology and Center for Human Genome Research, Huazhong University of Science and Technology, Wuhan, Hubei, China.

American Journal of Medical Genetics. Part A
|September 1, 2021
PubMed

Keywords:
exome sequencinggenome sequencinglinkage analysismicrodeletionsynpolydactyly

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