WP4949 - 16p11.2 proximal deletion syndrome - Homo sapiens
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16p11.2 proximal deletion syndrome is a rare genetic disorder (copy number variation) caused by a deletion in the region of chromosome 16 from 29,592,751 to 30,190,593 bp (GRCh37). The breakpoints are from: Dell'Edera 2018 PMID: 29609622.
创建时间：
2025-04-17
