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Evidence of founder mutations in Finnish BRCA1 and BRCA2 families
scientific article
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instance of
scholarly article
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title
Evidence of founder mutations in Finnish BRCA1 and BRCA2 families
(English)
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main subject
Finland
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author
Minna Pöyhönen
object named as
M Pöyhönen
series ordinal
4
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Robert Winqvist
series ordinal
11
object named as
R Winqvist
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author name string
P Huusko
series ordinal
1
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K Pääkkönen
series ordinal
2
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V Launonen
series ordinal
3
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G Blanco
series ordinal
5
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A Kauppila
series ordinal
6
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U Puistola
series ordinal
7
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H Kiviniemi
series ordinal
8
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M Kujala
series ordinal
9
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J Leisti
series ordinal
10
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language of work or name
English
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publication date
June 1998
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published in
American Journal of Human Genetics
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volume
62
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issue
6
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page(s)
1544-8
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cites work
Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of the breast cancer susceptibility gene BRCA2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
BRCA2 germline mutations in male breast cancer cases and breast cancer families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Breast cancer genes--what are the real risks?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Founding mutations and Alu-mediated recombination in hereditary colon cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: comparison with denaturing gradient gel electrophoresis and nucleotide sequencing
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disease gene mapping in isolated human populations: the example of Finland
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F301880
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1086/301880
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PMC publication ID
1377159
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PubMed publication ID
9585608
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ResearchGate publication ID
13697711
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