A novel 1p13.2 deletion associates with neurodevelopmental disorders in a three-generation pedigree
Abstract Background A multitude of studies have highlighted that copy number variants (CNVs) are associated with neurodevelopmental disorders (NDDs) characterized by a wide range of clinical characteristics. Benefiting from CNV calling from WES data, WES has emerged as a more powerful and cost-effec...
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| Main Authors: | , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2023-05-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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