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Germline DNA copy number variation in familial and early-onset breast cancer
INTRODUCTION: Genetic factors predisposing individuals to cancer remain elusive in the majority of patients with a familial or clinical history suggestive of hereditary breast cancer. Germline DNA copy number variation (CNV) has recently been implicated in predisposition to cancers such as neuroblas...
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| Main Authors: | , , , , , , , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2012
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3496142/ https://ncbi.nlm.nih.gov/pubmed/22314128 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/bcr3109 |
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