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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

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

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

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

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

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

PDF] Founder BRCA 1 / 2 mutations in the Europe : implications for  hereditary breast-ovarian cancer prevention and control | Semantic Scholar
PDF] Founder BRCA 1 / 2 mutations in the Europe : implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar

PDF] Prevalence and Penetrance of BRCA1 and BRCA2 Germline Mutations in  Colombian Breast Cancer Patients | Semantic Scholar
PDF] Prevalence and Penetrance of BRCA1 and BRCA2 Germline Mutations in Colombian Breast Cancer Patients | Semantic Scholar

GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS

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

GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS

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

A Reference System for BRCA Mutation Detection Based on Next-Generation  Sequencing in the Chinese Population - The Journal of Molecular Diagnostics
A Reference System for BRCA Mutation Detection Based on Next-Generation Sequencing in the Chinese Population - The Journal of Molecular Diagnostics

Truncating mutations in BRCA1, BRCA2 and PALB2 among 40 TNBC patients. |  Download Table
Truncating mutations in BRCA1, BRCA2 and PALB2 among 40 TNBC patients. | Download Table

Recurrent mutation testing of BRCA1 and BRCA2 in asian breast cancer  patients identify carriers in those with presumed low risk by family  history - Document - Gale OneFile: Health and Medicine
Recurrent mutation testing of BRCA1 and BRCA2 in asian breast cancer patients identify carriers in those with presumed low risk by family history - Document - Gale OneFile: Health and Medicine

GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS
GENETIC VARIANTS: SIMPLE ENOUGH FOR MY DAUGHTER'S 4TH GRADE CLASS

Genes | Free Full-Text | Differences in Ovarian and Other Cancers Risks by  Population and BRCA Mutation Location | HTML
Genes | Free Full-Text | Differences in Ovarian and Other Cancers Risks by Population and BRCA Mutation Location | HTML

Recurrent mutation testing of BRCA1 and BRCA2 in asian breast cancer  patients identify carriers in those with presumed low risk by family  history - Document - Gale OneFile: Health and Medicine
Recurrent mutation testing of BRCA1 and BRCA2 in asian breast cancer patients identify carriers in those with presumed low risk by family history - Document - Gale OneFile: Health and Medicine

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

Common mutation types of BRCA1 or BRCA2 genes in the BIC database. |  Download Scientific Diagram
Common mutation types of BRCA1 or BRCA2 genes in the BIC database. | Download Scientific Diagram

Improving sequence variant descriptions in mutation databases and  literature using the Mutalyzer sequence variation nomenclature checker -  Wildeman - 2008 - Human Mutation - Wiley Online Library
Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker - Wildeman - 2008 - Human Mutation - Wiley Online Library

Experimentally observed effects on mRNA splicing of group A variants... |  Download Table
Experimentally observed effects on mRNA splicing of group A variants... | Download Table

ENIGMA variant classification process. ENIGMA, Evidence-based Network... |  Download Scientific Diagram
ENIGMA variant classification process. ENIGMA, Evidence-based Network... | Download Scientific Diagram

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

Novel variants of uncertain clinical significance (VUS) in Greek... |  Download Table
Novel variants of uncertain clinical significance (VUS) in Greek... | Download Table

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