Identifying chromosome 17q11.2 variations
收藏NIAID Data Ecosystem2026-03-12 收录
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资源简介：
The purpose of this study is to identify the prevalence, genetic characteristics and clinical phenotype of 17p11.2 deletion/duplication in Chinese children with development delay and in fetuses with potential congenital defects.
创建时间：
2021-05-11
