WP5345 - 1p36 copy number variation syndrome - Homo sapiens
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https://www.ndexbio.org/viewer/networks/3dd891c7-1439-11f0-9806-005056ae3c32
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资源简介：
1p36 deletion or duplication syndromes are a rare genetic disorders caused by a deletion or duplication of the most distal light band of the short arm of chromosome 1.
创建时间：
2025-04-17
