Characterizing Disease-Causing Variants Using Personal Genomes with Large Recurrent Deletions
收藏NIAID Data Ecosystem2026-04-29 收录
下载链接：
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs002613.v1.p1
下载链接
链接失效反馈官方服务：
资源简介：
]]>
Inclusion criteria: individuals and family members with the recurrent 17q12 deletions or the recurrent 1q21.1 deletions. ]]>
创建时间：
2021-09-16
