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Large genomic rearrangements of both BRCA2 and BRCA1 are a feature of the inherited breast/ovarian cancer phenotype in selected families

Introduction: A strong family history of breast and/or ovarian cancer can often be explained by small insertions, deletions, or substitutions in BRCA1 or BRCA2 and large genomic rearrangements in BRCA1. However, there is little evidence that genomic rearrangements are a major factor in BRCA2 associa...

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Bibliografski detalji
Glavni autori: Woodward, A, Davis, T, Silva, A, kConFab, I, Kirk, J, Leary, J
Format: Artigo
Jezik:Inglês
Izdano: BMJ Group 2005
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1736061/
https://ncbi.nlm.nih.gov/pubmed/15863663
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.027961
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