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Effects of BRCA1 and BRCA2 mutations on female fertilityBRCA genetic screening in Middle Eastern and North African: mutational spectrum and founder BRCA1 mutation (c.798_799delTT) in North AfricanDistribution of BRCA1 and BRCA2 Mutations in Asian Patients with Breast CancerSapacitabine for cancerThe cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics dataPrevalence of the most frequent BRCA1 mutations in Polish populationDeriving a mutation index of carcinogenicity using protein structure and protein interfacesBeyond Our Borders? Public Resistance to Global Genomic Data SharingMutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological Sense.Personalized prostate cancer screening among men with high risk genetic predisposition- study protocol for a prospective cohort study.Free the DataProtein disorder in the human diseasome: unfoldomics of human genetic diseases.How many genetic variants remain to be discovered?Detection of BRCA1 and BRCA2 Ashkenazi Jewish founder mutations in formalin-fixed paraffin-embedded tissues using conventional PCR and heteroduplex/amplicon size differencesToward classification of BRCA1 missense variants using a biophysical approach.Identity by descent mapping of founder mutations in cancer using high-resolution tumor SNP data.Full-exon pyrosequencing screening of BRCA germline mutations in Mexican women with inherited breast and ovarian cancer.Founder and Recurrent Mutations in BRCA1 and BRCA2 Genes in Latin American Countries: State of the Art and Literature Review.Mutational analysis of BRCA1 and BRCA2 in hereditary breast and ovarian cancer families from Asturias (Northern Spain).Perfluorinated compounds are related to breast cancer risk in Greenlandic Inuit: a case control study.Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from Greece.Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countriesGenetics of breast cancer: a topic in evolution.Tracking of the origin of recurrent mutations of the BRCA1 and BRCA2 genes in the North-East of Italy and improved mutation analysis strategy.Hereditary breast-ovarian cancer syndrome in Russia.Cumulative BRCA mutation analysis in the Greek population confirms that homogenous ethnic background facilitates genetic testing.Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas.Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.Genetic testing and first presymptomatic diagnosis in Moroccan families at high risk for breast/ovarian cancer.Novel sequence variants and common recurrent polymorphisms of BRCA2 in Sri Lankan breast cancer patients and a family with BRCA1 mutations.Prevalance of BRCA1 and BRCA2 mutations in familial breast cancer patients in LebanonSeventeen years after BRCA1: what is the BRCA mutation status of the breast cancer patients in Africa? - a systematic review.A new rapid methodological strategy to assess BRCA mutational status.Prevalence of the BRCA1 c.68_69delAG (BIC: 185delAG) mutation in women with breast cancer from north-central Poland and a review of the literature on other regions of the country.BRCA1 and BRCA2 rearrangements in Brazilian individuals with Hereditary Breast and Ovarian Cancer Syndrome.Haplotype analysis of BRCA1 intragenic markers in Iranian patients with familial breast and ovarian cancerBreast cancer therapy for BRCA1 carriers: moving towards platinum standard?Genetic variation of the brca1 and brca2 genes in macedonian patientsContribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases.The Clinical Significance of Unknown Sequence Variants in BRCA Genes.
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Founder mutations in BRCA1 and BRCA2 genes.
@en
type
label
Founder mutations in BRCA1 and BRCA2 genes.
@en
prefLabel
Founder mutations in BRCA1 and BRCA2 genes.
@en
P2093
P356
P1433
P1476
Founder mutations in BRCA1 and BRCA2 genes
@en
P2093
G Badalamenti
P304
P356
10.1093/ANNONC/MDM234
P478
18 Suppl 6
P577
2007-06-01T00:00:00Z