Home

West jam Stationair mutations hgvs bic delicatesse projector Hollywood

BRCA1 variants identified in the analyzed population . by dHPLC/Sanger... | Download Table
BRCA1 variants identified in the analyzed population . by dHPLC/Sanger... | Download Table

PDF] Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar
PDF] Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar

A computational model for classification of BRCA2 variants using mouse embryonic stem cell-based functional assays | npj Genomic Medicine
A computational model for classification of BRCA2 variants using mouse embryonic stem cell-based functional assays | npj Genomic Medicine

High prevalence of BRCA1 founder mutations in Greek breast/ovarian families
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families

PDF] Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas | Semantic Scholar
PDF] Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas | Semantic Scholar

Online Resource 1A: BRCA1 mutations tested Mutation (BIC
Online Resource 1A: BRCA1 mutations tested Mutation (BIC

Frontiers | Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15 | Genetics
Frontiers | Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15 | Genetics

Comprehensive prediction of mRNA splicing effects of BRCA1 and BRCA2 variants - Mucaki - 2011 - Human Mutation - Wiley Online Library
Comprehensive prediction of mRNA splicing effects of BRCA1 and BRCA2 variants - Mucaki - 2011 - Human Mutation - Wiley Online Library

Functional Assays for Analysis of Variants of Uncertain Significance in BRCA2 - Guidugli - 2014 - Human Mutation - Wiley Online Library
Functional Assays for Analysis of Variants of Uncertain Significance in BRCA2 - Guidugli - 2014 - Human Mutation - Wiley Online Library

Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis

Frameshift mutations detected in BRCA genes | Download Table
Frameshift mutations detected in BRCA genes | Download Table

Prevalence of BRCA1/2 mutations in sporadic breast/ovarian cancer patients and identification of a novel de novo BRCA1 mutation in a patient diagnosed with late onset breast and ovarian cancer: implications for genetic
Prevalence of BRCA1/2 mutations in sporadic breast/ovarian cancer patients and identification of a novel de novo BRCA1 mutation in a patient diagnosed with late onset breast and ovarian cancer: implications for genetic

Table 4 from The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population | Semantic Scholar
Table 4 from The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population | Semantic Scholar

Frontiers | Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays | Genetics
Frontiers | Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays | Genetics

Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women – topic of research paper in Biological sciences. Download scholarly article PDF and read for free
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women – topic of research paper in Biological sciences. Download scholarly article PDF and read for free

The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries - Laitman - 2019 - Human Mutation - Wiley Online Library
The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries - Laitman - 2019 - Human Mutation - Wiley Online Library

PDF] Recurrent mutation testing of BRCA1 and BRCA2 in Asian breast cancer patients identify carriers in those with presumed low risk by family history | Semantic Scholar
PDF] Recurrent mutation testing of BRCA1 and BRCA2 in Asian breast cancer patients identify carriers in those with presumed low risk by family history | Semantic Scholar

PDF] Novel BRCA1 and BRCA2 genomic rearrangements in Southern Chinese breast/ovarian cancer patients | Semantic Scholar
PDF] Novel BRCA1 and BRCA2 genomic rearrangements in Southern Chinese breast/ovarian cancer patients | Semantic Scholar

PDF] The Clinical Significance of Unknown Sequence Variants in BRCA Genes | Semantic Scholar
PDF] The Clinical Significance of Unknown Sequence Variants in BRCA Genes | Semantic Scholar

Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes. - Abstract - Europe PMC
Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes. - Abstract - Europe PMC

PDF) Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families | Petra Cerkovnik - Academia.edu
PDF) Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families | Petra Cerkovnik - Academia.edu

Germline mutational spectrum in Armenian breast cancer patients suspected of hereditary breast and ovarian cancer | Human Genome Variation
Germline mutational spectrum in Armenian breast cancer patients suspected of hereditary breast and ovarian cancer | Human Genome Variation

Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients. - Abstract - Europe PMC
Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients. - Abstract - Europe PMC

Purpose
Purpose

Table 1 from A multi-gene panel study in hereditary breast and ovarian cancer in Colombia | Semantic Scholar
Table 1 from A multi-gene panel study in hereditary breast and ovarian cancer in Colombia | Semantic Scholar