Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study ; volume:11 ; number:1 ; day:19 ; month:4 ; year:2021 ; pages:1-8 ; date:12.2021
Scientific reports ; 11, Heft 1 (19.4.2021), 1-8, 12.2021
- Creator
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Kim, Joo Heung
Park, Sunggyun
Park, Hyung Seok
Park, Ji Soo
Lee, Seung-Tae
Kim, Sung-Won
Lee, Jong Won
Lee, Min Hyuk
Park, Sue K.
Noh, Woo-Chul
Choi, Doo Ho
Han, Wonshik
Jung, Sung Hoo
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41598-021-87792-w
- URN
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urn:nbn:de:101:1-2412030919154.581096614223
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:25 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kim, Joo Heung
- Park, Sunggyun
- Park, Hyung Seok
- Park, Ji Soo
- Lee, Seung-Tae
- Kim, Sung-Won
- Lee, Jong Won
- Lee, Min Hyuk
- Park, Sue K.
- Noh, Woo-Chul
- Choi, Doo Ho
- Han, Wonshik
- Jung, Sung Hoo
- SpringerLink (Online service)
Other Objects (12)
Author Correction: Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study
Trans-activation-based risk assessment of BRCA1 BRCT variants with unknown clinical significance
Variants of cancer susceptibility genes in Korean BRCA1/2 mutation-negative patients with high risk for hereditary breast cancer
Markers of Hereditary Thrombophilia with Unclear Significance
Gene Expression Profiling in Hereditary, BRCA1-linked Breast Cancer: Preliminary Report
How does re-classification of variants of unknown significance (VUS) impact the management of patients at risk for hereditary breast cancer?
Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline
Preliminary molecular evidence associating a novel BRCA1 synonymous variant with hereditary ovarian cancer syndrome
BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratories
A new bioinformatics tool to help assess the significance of BRCA1 variants
Clinical and genetic analyses of three Korean families with hereditary hemorrhagic telangiectasia
Functional and evolutionary significance of unknown genes from uncultivated taxa
Author Correction: Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study
Trans-activation-based risk assessment of BRCA1 BRCT variants with unknown clinical significance
Variants of cancer susceptibility genes in Korean BRCA1/2 mutation-negative patients with high risk for hereditary breast cancer
Markers of Hereditary Thrombophilia with Unclear Significance
Gene Expression Profiling in Hereditary, BRCA1-linked Breast Cancer: Preliminary Report
How does re-classification of variants of unknown significance (VUS) impact the management of patients at risk for hereditary breast cancer?
Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline
Preliminary molecular evidence associating a novel BRCA1 synonymous variant with hereditary ovarian cancer syndrome
BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratories
A new bioinformatics tool to help assess the significance of BRCA1 variants
Clinical and genetic analyses of three Korean families with hereditary hemorrhagic telangiectasia
Functional and evolutionary significance of unknown genes from uncultivated taxa
Author Correction: Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study
Trans-activation-based risk assessment of BRCA1 BRCT variants with unknown clinical significance
Variants of cancer susceptibility genes in Korean BRCA1/2 mutation-negative patients with high risk for hereditary breast cancer
Markers of Hereditary Thrombophilia with Unclear Significance
Gene Expression Profiling in Hereditary, BRCA1-linked Breast Cancer: Preliminary Report
How does re-classification of variants of unknown significance (VUS) impact the management of patients at risk for hereditary breast cancer?
Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline
Preliminary molecular evidence associating a novel BRCA1 synonymous variant with hereditary ovarian cancer syndrome
BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratories
A new bioinformatics tool to help assess the significance of BRCA1 variants
Clinical and genetic analyses of three Korean families with hereditary hemorrhagic telangiectasia