WP5346 - 8p23.1 copy number variation syndrome - Homo sapiens
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https://www.ndexbio.org/viewer/networks/e7e95d57-1438-11f0-9806-005056ae3c32
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资源简介：
Pathways of relevant genes on the chromosome 8p23.1 duplication / deletion syndrome. Patients with a deletion often suffer from diaphragmatic hernia (CDH) and cardiac defects.
创建时间：
2025-04-17
