Synpolydacty type I
收藏NIAID Data Ecosystem2026-05-26 收录
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资源简介：
We did whole genome sequencing of a patient with synpolydactyly type I disease, the family we studies have eight affected persons with the same disease. We found mutaion in exon 1 of HOXD13 gene in all affected members.
创建时间：
2019-06-01
