(Q38208233)

31 August 2017

Collaboration of colorado cancer genetic counselors to integrate next generation sequencing panels into clinical practice (English)

1 reference

31 August 2017

1 reference

10

A Kulchak Rahm

1 reference

31 August 2017

K Wolfe Schneider

1

1 reference

31 August 2017

A Anguiano

2

1 reference

31 August 2017

L Axell

3

1 reference

31 August 2017

C Barth

4

1 reference

31 August 2017

K Crow

5

1 reference

31 August 2017

M Gilstrap

6

1 reference

31 August 2017

B A Hamlington

7

1 reference

31 August 2017

S Lesh

8

1 reference

31 August 2017

L Mullineaux

9

1 reference

31 August 2017

E Strait

11

1 reference

31 August 2017

M Freivogel

12

1 reference

31 August 2017

1 May 2014

1 reference

Journal of Genetic Counseling

31 August 2017

1 reference

31 August 2017

23

1 reference

31 August 2017

4

1 reference

31 August 2017

640-646

1 reference

Hereditary breast cancer: the era of new susceptibility genes

31 August 2017

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9718-3

NSGC practice guideline: risk assessment and genetic counseling for hereditary breast and ovarian cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9718-3

The prevalence of CDKN2A germ-line mutations and relative risk for cutaneous malignant melanoma: an international population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9718-3

Evaluating the utility of personal genomic information

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9718-3

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9718-3

Review of massively parallel DNA sequencing technologies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9718-3

Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9718-3

Mutation screening of RAD51C in male breast cancer patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9718-3

Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9718-3

Ten genes for inherited breast cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9718-3

A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24781714

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24781714

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10897-014-9718-3

1 reference

31 August 2017

1 reference