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Benign copy number changes in clinical cytogenetic diagnostics by array CGH
A database of apparently benign copy number variants (bCNVs) detected by a Spectral Genomics Inc./PerkinElmer BAC array platform has been maintained through the University of Utah Comparative Genomic Hybridization laboratory since 2005. The target population for this database represents 1,275 patien...
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| 主要な著者: | , , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
S. Karger AG
2009
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2920185/ https://ncbi.nlm.nih.gov/pubmed/19287143 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000184696 |
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