Identification of a founder BRCA2 mutation in Sardinian breast cancer families (Q60570162)

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24 December 2019

title

Identification of a founder BRCA2 mutation in Sardinian breast cancer families (English)

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24 December 2019

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2

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24 December 2019

author name string

Maria Monne

1

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24 December 2019

Patrizia Fancello

3

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24 December 2019

Maria Cristina Santona

4

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24 December 2019

Antonella Uras

5

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24 December 2019

Gennaro Landriscina

6

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24 December 2019

Giuseppe Mastio

7

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24 December 2019

Attilio Gabbas

8

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24 December 2019

publication date

1 January 2007

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24 December 2019

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24 December 2019

volume

6

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issue

1

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page(s)

73-79

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The same beta-globin gene mutation is present on nine different beta-thalassemia chromosomes in a Sardinian population

24 December 2019

cites work

1 reference

12 December 2020

Molecular characterization of wilson disease in the Sardinian population--evidence of a founder effect

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12 December 2020

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

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12 December 2020

The global burden of cancer

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12 December 2020

Identification of a founder BRCA2 mutation in Sardinia

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12 December 2020

A comparison of bayesian methods for haplotype reconstruction from population genotype data

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12 December 2020

Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study

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12 December 2020

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

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12 December 2020

BRCA1 and BRCA2 germline mutations in Sardinian breast cancer families and their implications for genetic counseling

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12 December 2020

Frequency of BRCA1/BRCA2 mutations in a population-based sample of young breast carcinoma cases

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12 December 2020

Estimates of the worldwide incidence of 25 major cancers in 1990.

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12 December 2020

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

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12 December 2020

Evidence of a founder mutation of BRCA1 in a highly homogeneous population from southern Italy with breast/ovarian cancer.

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12 December 2020

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

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12 December 2020

The genetic attributable risk of breast and ovarian cancer

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12 December 2020

Screening for mutations in exon 11 of the BRCA1 gene in 70 Italian breast and ovarian cancer patients by protein truncation test

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12 December 2020

Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?

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12 December 2020

Ethnic differences in cancer risk resulting from genetic variation

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12 December 2020

Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland

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12 December 2020

Major factors influencing linkage disequilibrium by analysis of different chromosome regions in distinct populations: demography, chromosome recombination frequency and selection

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12 December 2020

The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women

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12 December 2020

Inherited predisposition to breast and ovarian cancer

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12 December 2020

Population genetics of BRCA1 and BRCA2.

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12 December 2020

Identification of seven new BRCA1 germline mutations in Italian breast and breast/ovarian cancer families

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12 December 2020

10.1007/S10689-006-9107-7

Identifiers

DOI

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24 December 2019

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