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πρόωρος θλίψη πάτημα mutations hgvs bic Ατυχία Ελάχιστη πονοκέφαλο

Functional assays provide a robust tool for the clinical annotation of  genetic variants of uncertain significance | npj Genomic Medicine
Functional assays provide a robust tool for the clinical annotation of genetic variants of uncertain significance | npj Genomic Medicine

Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast  Cancer Patients Using Gene Sequencing and High Resolution DNA Melting  Analysis – topic of research paper in Biological sciences. Download  scholarly article PDF
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis – topic of research paper in Biological sciences. Download scholarly article PDF

Figures and data in Functional and mutational landscapes of BRCA1 for  homology-directed repair and therapy resistance | eLife
Figures and data in Functional and mutational landscapes of BRCA1 for homology-directed repair and therapy resistance | eLife

My Mutation
My Mutation

Cureus | Sociodemographic, Clinical, and Variation Outcomes for Breast  Cancer and Breast Cancer-Related Mutations in a Ten-Year Cohort From Neiva,  Huila, Colombia | Article
Cureus | Sociodemographic, Clinical, and Variation Outcomes for Breast Cancer and Breast Cancer-Related Mutations in a Ten-Year Cohort From Neiva, Huila, Colombia | Article

Prevalence and spectrum of BRCA germline variants in mainland Chinese  familial breast and ovarian cancer patients | Oncotarget
Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients | Oncotarget

Reported prevalence of BRCA1 founder mutations in the Polish population. |  Download Scientific Diagram
Reported prevalence of BRCA1 founder mutations in the Polish population. | Download Scientific Diagram

How to read variant information in the rare diseases test reports…
How to read variant information in the rare diseases test reports…

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

Identification of the most common BRCA alterations through analysis of  germline mutation databases: Is droplet digital PCR an additional strategy  for the assessment of such alterations in breast and ovarian cancer  families?
Identification of the most common BRCA alterations through analysis of germline mutation databases: Is droplet digital PCR an additional strategy for the assessment of such alterations in breast and ovarian cancer families?

Reported prevalence of BRCA1 founder mutations in the Polish population. |  Download Scientific Diagram
Reported prevalence of BRCA1 founder mutations in the Polish population. | 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

Identification of the most common BRCA alterations through analysis of  germline mutation databases: Is droplet digital PCR an additional strategy  for the assessment of such alterations in breast and ovarian cancer  families?
Identification of the most common BRCA alterations through analysis of germline mutation databases: Is droplet digital PCR an additional strategy for the assessment of such alterations in breast and ovarian cancer families?

Genes | Free Full-Text | BRCA1/2 Mutations in Vietnamese Patients with  Hereditary Breast and Ovarian Cancer Syndrome
Genes | Free Full-Text | BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome

Cancers | Free Full-Text | 5′ Region Large Genomic Rearrangements in the  BRCA1 Gene in French Families: Identification of a Tandem Triplication and  Nine Distinct Deletions with Five Recurrent Breakpoints
Cancers | Free Full-Text | 5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints

BRCA Exchange
BRCA Exchange

The occurrence of germline BRCA1 and BRCA2 sequence alterations in  Slovenian population – topic of research paper in Biological sciences.  Download scholarly article PDF and read for free on CyberLeninka open  science
The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on CyberLeninka open science

Absence of BRCA/FMR1 Correlations in Women with Ovarian Cancers | PLOS ONE
Absence of BRCA/FMR1 Correlations in Women with Ovarian Cancers | PLOS ONE

Germ line BRCA2 pathogenic mutations in breast and ovarian cancer... |  Download Table
Germ line BRCA2 pathogenic mutations in breast and ovarian cancer... | Download Table

Table 2 from Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer  from 'unknown significance' to 'Likely pathogenic' based on clinical  evidence in Korea. | Semantic Scholar
Table 2 from Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea. | Semantic Scholar

How to read variant information in the rare diseases test reports…
How to read variant information in the rare diseases test reports…

Spectrum of the Mutations in <fc>B</fc>ernard&#x02013;<fc>S</fc>oulier  Syndrome
Spectrum of the Mutations in <fc>B</fc>ernard&#x02013;<fc>S</fc>oulier Syndrome

dbBRCA-Asian
dbBRCA-Asian

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

P/LP variants. cDNA and Protein changes are named according to HGVS... |  Download Table
P/LP variants. cDNA and Protein changes are named according to HGVS... | Download Table

Comparative In Vitro and In Silico Analyses of Variants in Splicing Regions  of BRCA1 and BRCA2 Genes and Characterization of Novel Pathogenic Mutations  | PLOS ONE
Comparative In Vitro and In Silico Analyses of Variants in Splicing Regions of BRCA1 and BRCA2 Genes and Characterization of Novel Pathogenic Mutations | PLOS ONE

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of  unknown clinical significance in unilateral and bilate
Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilate