The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?
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The biological effects and clinical implications of BRCA mutations: where do we go from here?Hereditary ovarian cancer: not only BRCA 1 and 2 genes.Double PALB2 and BRCA1/BRCA2 mutation carriers are rare in breast cancer and breast-ovarian cancer syndrome families from the French Canadian founder populationNext-Generation Testing for Cancer Risk: Perceptions, Experiences, and Needs Among Early Adopters in Community Healthcare SettingsDevelopment of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibilityNext-generation sequencing for inherited breast cancer risk: counseling through the complexity.Testing for Hereditary Breast Cancer: Panel or Targeted Testing? Experience from a Clinical Cancer Genetics Practice.Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance.Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel.
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P2860
The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?
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article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artículo científico
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name
The impact of next generation ...... remely rare genetic variation?
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type
label
The impact of next generation ...... remely rare genetic variation?
@en
prefLabel
The impact of next generation ...... remely rare genetic variation?
@en
P2860
P356
P1433
P1476
The impact of next generation ...... remely rare genetic variation?
@en
P2093
F S M Hilbers
M P G Vreeswijk
P2860
P304
P356
10.1111/CGE.12256
P577
2013-09-12T00:00:00Z