11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies
收藏NIAID Data Ecosystem2026-03-12 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP310312
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资源简介：
The molecular cytogenetic approach was helpful in identifying the genetic aetiology of 11p11.12p12 duplication syndrome and potential candidate genes with triplosensitive effects involved in 11p11.12p12 duplication.
创建时间：
2021-03-12
