(Q48093932)

English

Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome.

scientific article published on 5 December 2015

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26637299%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26637299%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Carlos J Gallego

1

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1 March 2020

David L Veenstra

9

object named as

David L Veenstra

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1 March 2020

author name string

Matthew L Perez

2

1 reference

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1 March 2020

Amber Burt

3

1 reference

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1 March 2020

Laura M Amendola

4

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1 March 2020

Brian H Shirts

5

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1 March 2020

Colin C Pritchard

6

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1 March 2020

Fuki M Hisama

7

1 reference

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1 March 2020

Robin L Bennett

8

1 reference

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1 March 2020

Gail P Jarvik

10

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1 March 2020

publication date

5 December 2015

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1 March 2020

Journal of Genetic Counseling

1 reference

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1 March 2020

25

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1 March 2020

3

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1 March 2020

515-519

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1 March 2020

Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory.

1 reference

https://api.crossref.org/works/10.1007%2FS10897-015-9902-0

21 January 2018

Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes

1 reference

https://api.crossref.org/works/10.1007%2FS10897-015-9902-0

21 January 2018

Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis

1 reference

https://api.crossref.org/works/10.1007%2FS10897-015-9902-0

21 January 2018

Human genome sequencing in health and disease

1 reference

https://api.crossref.org/works/10.1007%2FS10897-015-9902-0

21 January 2018

Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS10897-015-9902-0

21 January 2018

ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing

1 reference

https://api.crossref.org/works/10.1007%2FS10897-015-9902-0

21 January 2018

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

1 reference

https://api.crossref.org/works/10.1007%2FS10897-015-9902-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10897-015-9902-0

21 January 2018

The evolution of cancer risk assessment in the era of next generation sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/26637299

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impact of NGS in the medical sciences: Genetic syndromes with an increased risk of developing cancer as an example of the use of new technologies

1 reference

https://pubmed.ncbi.nlm.nih.gov/26637299

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10897-015-9902-0

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26637299%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26637299%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

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