Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH
Detection of predisposing copy number variants (CNV) in 330 families affected with hereditary breast and ovarian cancer (HBOC).
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| Main Authors: | , , , , , , , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
31 August 2016
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| In: |
Breast cancer research and treatment
Year: 2016, Volume: 159, Issue: 3, Pages: 585-590 |
| ISSN: | 1573-7217 |
| DOI: | 10.1007/s10549-016-3956-z |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s10549-016-3956-z
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| Author Notes: | Karl Hackmann, Franziska Kuhlee, Elitza Betcheva-Krajcir, Anne-Karin Kahlert, Luisa Mackenroth, Barbara Klink, Nataliya Di Donato, Andreas Tzschach, Karin Kast, Pauline Wimberger, Evelin Schrock, Andreas Rump |
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