High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
about
Cumulative BRCA mutation analysis in the Greek population confirms that homogenous ethnic background facilitates genetic testing.Disease evolution and heterogeneity in bilateral breast cancer.The fate of BRCA1-related germline mutations in triple-negative breast tumors.Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation.Germline deleterious mutations in genes other than BRCA2 are infrequent in male breast cancer.46,XY disorder of sex development due to 17-beta hydroxysteroid dehydrogenase type 3 deficiency in an infant of Greek origin.BRCA1 and BRCA2 germline variants in breast cancer patients from the Republic of Macedonia.Multicenter cross-sectional screening of the BRCA gene for Chinese high hereditary risk breast cancer populations.
P2860
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P2860
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
description
2013 nî lūn-bûn
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2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
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2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
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2013年學術文章
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2013年學術文章
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name
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
@en
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
@nl
type
label
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
@en
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
@nl
prefLabel
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
@en
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
@nl
P2093
P2860
P50
P356
P1433
P1476
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
@en
P2093
A P Tsiftsoglou
A-V Stavropoulou
C Dimitrakakis
M Tsitlaidou
O Triantafyllidou
S Droufakou
P2860
P356
10.1111/CGE.12274
P577
2013-10-20T00:00:00Z