Evidence of a founder BRCA1 mutation in Scotland (Q24649433)

3

object named as

D M Black

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author name string

A Liede

1

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B Cohen

2

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R H Davidson

4

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A Renwick

5

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E Hoodfar

6

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O I Olopade

7

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M Micek

8

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V Anderson

9

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R De Mey

10

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A Fordyce

11

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E Warner

12

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J L Dann

13

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M C King

14

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B Weber

15

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C M Steel

British Journal of Cancer

17

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language of work or name

English

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publication date

February 2000

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published in

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volume

82

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issue

3

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page(s)

705-11

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cites work

Frequently occurring germ-line mutations of the BRCA1 gene in ovarian cancer families from Russia

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Study of a single BRCA2 mutation with high carrier frequency in a small population

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Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families

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The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

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BRCA1 and BRCA2 in breast cancer families from Wales: moderate mutation frequency and two recurrent mutations in BRCA1

7 April 2017

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Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families

28 September 2017

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BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

28 September 2017

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BRCA1 5382insC mutation in sporadic and familial breast and ovarian carcinoma in Scotland

28 September 2017

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Inactivation of the mouse Brca1 gene leads to failure in the morphogenesis of the egg cylinder in early postimplantation development.

28 September 2017

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Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study

28 September 2017

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Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

28 September 2017

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Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families

28 September 2017

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The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

28 September 2017

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Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families

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Analysis of BRCA1 and BRCA2 mutations in Hungarian families with breast or breast-ovarian cancer

28 September 2017

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Population genetics of BRCA1 and BRCA2.

30 May 2018

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Public records and recognition of genetic disease in Scotland

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A breast cancer patient of Scottish descent with germ-line mutations in BRCA1 and BRCA2.

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Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

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