Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene (Q71955901)

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22 October 2019

title

Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene (English)

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22 October 2019

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8

Easton D

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22 October 2019

7

Stratton MR

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1

Gayther SA

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22 October 2019

author name string

Mangion J

2

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22 October 2019

Russell P

3

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22 October 2019

Seal S

4

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22 October 2019

Barfoot R

5

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22 October 2019

Ponder BA

6

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publication date

1 January 1997

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22 October 2019

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22 October 2019

volume

15

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issue

1

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page(s)

103-105

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Identification of the breast cancer susceptibility gene BRCA2

22 October 2019

cites work

1 reference

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7 January 2021

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

1 reference

https://api.crossref.org/works/10.1038%2FNG0197-103

7 January 2021

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes

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7 January 2021

Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families

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7 January 2021

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

1 reference

https://api.crossref.org/works/10.1038%2FNG0197-103

7 January 2021

Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation

1 reference

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7 January 2021

Growth retardation and tumour inhibition by BRCA1.

1 reference

https://api.crossref.org/works/10.1038%2FNG0197-103

7 January 2021

The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds

1 reference

https://api.crossref.org/works/10.1038%2FNG0197-103

7 January 2021

A polymorphic stop codon in BRCA2

1 reference

https://api.crossref.org/works/10.1038%2FNG0197-103

7 January 2021

BRCA2 germline mutations in male breast cancer cases and breast cancer families

1 reference

https://api.crossref.org/works/10.1038%2FNG0197-103

7 January 2021

Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer

1 reference

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7 January 2021

Regionally clustered APC mutations are associated with a severe phenotype and occur at a high frequency in new mutation cases of adenomatous polyposis coli.

1 reference

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7 January 2021

Alleles of the APC gene: an attenuated form of familial polyposis

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7 January 2021

Identifiers

DOI

10.1038/NG0197-103

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988179%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

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