SMC2: a candidate gene associated with Cornelia de Lange Syndrome. Homo sapiens
收藏NIAID Data Ecosystem2026-03-08 收录
官方服务：
资源简介：
whole-genome aCGH analysis also showed us that the patient carried a 12.01-1M Mb deletion region at chromosome bands 9q31.1-q32 (105,190,105-117,195,154). The deleted region encompasses 22 genes including SMC2 Overall design: Two-condition Samples, Cornelia de Lange Syndrome vs. Normal cells.
创建时间：
2014-01-23
