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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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Bibliographic Details
Main Authors: Hackmann, Karl (Author) , Kuhlee, Franziska (Author) , Betcheva-Krajcir, Elitza (Author) , Kahlert, Anne-Karin (Author) , Mackenroth, Luisa (Author) , Klink, Barbara (Author) , Di Donato, Nataliya (Author) , Tzschach, Andreas (Author) , Kast, Karin (Author) , Wimberger, Pauline (Author) , Schröck, Evelin (Author) , Rump, Andreas (Author)
Format: Article (Journal)
Language:English
Published: 31 August 2016
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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Summary:Detection of predisposing copy number variants (CNV) in 330 families affected with hereditary breast and ovarian cancer (HBOC).
Item Description:Gesehen am 04.09.2020
Physical Description:Online Resource
ISSN:1573-7217
DOI:10.1007/s10549-016-3956-z

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