Identifying chromosome 17q11.2 variations
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA729174
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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
