Use of panel tests in place of single gene tests in the cancer genetics clinic-Reference-Cited by-同舟云学术

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Use of panel tests in place of single gene tests in the cancer genetics clinic

Published:2014-10-16 Issue:3 Volume:88 Page:278-282
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Yorczyk A.¹²,Robinson L.S.¹²,Ross T.S.¹²

Affiliation:

1. Department of Cancer Genetics University of Texas Southwestern Medical Center's Harold Simmons Comprehensive Cancer Center Dallas TX USA

2. Department of Cancer Genetics University of Texas Southwestern Medical Center's Moncrief Cancer Institute Fort Worth TX USA

Funder

National Institutes of Health

Burrroughs Welcome Fund

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.12488

Reference9 articles.

1. Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

2. Integrating next-generation sequencing into the diagnostic testing of inherited cancer predisposition

3. Multiplex Genetic Testing for Cancer Susceptibility: Out on the High Wire Without a Net?

4. Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

5. The integration of next-generation sequencing panels in the clinical cancer genetics practice: an institutional experience

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