[HTML][HTML] Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context

ER Thompson, KL Gorringe, SM Rowley, N Li… - Scientific reports, 2015 - nature.com
The breast cancer predisposition gene, BRCA2, has a large number of genetic variants of
unknown effect. The variant rs11571833, an A> T transversion in the final exon of the gene …

[HTML][HTML] Reevaluation of the BRCA2 truncating allele c. 9976A> T (p. Lys3326Ter) in a familial breast cancer context

ER Thompson, KL Gorringe, SM Rowley, N Li… - Scientific …, 2015 - ncbi.nlm.nih.gov
The breast cancer predisposition gene, BRCA2, has a large number of genetic variants of
unknown effect. The variant rs11571833, an A> T transversion in the final exon of the gene …

Reevaluation of the BRCA2 truncating allele c. 9976A> T (p. Lys3326Ter) in a familial breast cancer context

ER Thompson, KL Gorringe, SM Rowley… - Scientific …, 2015 - pubmed.ncbi.nlm.nih.gov
The breast cancer predisposition gene, BRCA2, has a large number of genetic variants of
unknown effect. The variant rs11571833, an A> T transversion in the final exon of the gene …

[PDF][PDF] Reevaluation of the BRCA2 truncating allele c. 9976A> T (p. Lys3326Ter) in a familial breast cancer context

ER Thompson, KL Gorringe, SM Rowley, N Li… - minerva-access.unimelb.edu.au
Results As part of a panel screening approach in breast cancer cases ascertained through
familial cancer clinics in Australia, we evaluated the incidence of the BRCA2 variant …

Reevaluation of the BRCA2 truncating allele c. 9976A> T (p. Lys3326Ter) in a familial breast cancer context.

ER Thompson, KL Gorringe, SM Rowley… - Scientific …, 2015 - search.ebscohost.com
The breast cancer predisposition gene, BRCA2, has a large number of genetic variants of
unknown effect. The variant rs11571833, an A > T transversion in the final exon of the …

[PDF][PDF] Reevaluation of the BRCA2 truncating allele c. 9976A> T (p. Lys3326Ter) in a familial breast cancer context

ER Thompson, KL Gorringe, SM Rowley, N Li… - cyberleninka.org
Results As part of a panel screening approach in breast cancer cases ascertained through
familial cancer clinics in Australia, we evaluated the incidence of the BRCA2 variant …

[PDF][PDF] Reevaluation of the BRCA2 truncating allele c. 9976A> T (p. Lys3326Ter) in a familial breast cancer context

ER Thompson, KL Gorringe, SM Rowley, N Li… - 2015 - Citeseer
Results As part of a panel screening approach in breast cancer cases ascertained through
familial cancer clinics in Australia, we evaluated the incidence of the BRCA2 variant …

[PDF][PDF] Reevaluation of the BRCA2 truncating allele c. 9976A> T (p. Lys3326Ter) in a familial breast cancer context

ER Thompson, KL Gorringe, SM Rowley, N Li… - nova.newcastle.edu.au
Results As part of a panel screening approach in breast cancer cases ascertained through
familial cancer clinics in Australia, we evaluated the incidence of the BRCA2 variant …

Reevaluation of the BRCA2 truncating allele c. 9976A> T (p. Lys3326Ter) in a familial breast cancer context.

ER Thompson, KL Gorringe, SM Rowley, N Li… - Scientific …, 2015 - europepmc.org
The breast cancer predisposition gene, BRCA2, has a large number of genetic variants of
unknown effect. The variant rs11571833, an A> T transversion in the final exon of the gene …

[PDF][PDF] Reevaluation of the BRCA2 truncating allele c. 9976A> T (p. Lys3326Ter) in a familial breast cancer context

ER Thompson, KL Gorringe, SM Rowley, N Li… - researchgate.net
Results As part of a panel screening approach in breast cancer cases ascertained through
familial cancer clinics in Australia, we evaluated the incidence of the BRCA2 variant …