(Q37151115)

18 August 2017

Clinician perspectives about molecular genetic testing for heritable conditions and development of a clinician-friendly laboratory report (English)

1 reference

18 August 2017

Marc S Williams

12

0 references

Margaret M. McGovern

2

object named as

Margaret M McGovern

1 reference

18 August 2017

Ira M Lubin

1

1 reference

18 August 2017

Zoe Gibson

3

1 reference

18 August 2017

Susan J Gross

4

1 reference

18 August 2017

Elaine Lyon

5

1 reference

18 August 2017

Roberta A Pagon

6

1 reference

18 August 2017

Victoria M Pratt

7

1 reference

18 August 2017

Jamila Rashid

8

1 reference

18 August 2017

Colleen Shaw

9

1 reference

18 August 2017

Lander Stoddard

10

1 reference

18 August 2017

Tracy L Trotter

11

1 reference

18 August 2017

Jean Amos Wilson

13

1 reference

18 August 2017

Kenneth Pass

14

1 reference

18 August 2017

5 February 2009

1 reference

The Journal of Molecular Diagnostics

18 August 2017

1 reference

18 August 2017

11

1 reference

18 August 2017

2

1 reference

18 August 2017

162-171

1 reference

Ordering molecular genetic tests and reporting results: practices in laboratory and clinical settings

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Interest in the use of computerized patient portals: role of the provider-patient relationship

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

A review identifies and classifies reasons for ordering diagnostic tests.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

'Genetics home reference': helping patients understand the role of genetics in health and disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

GeneTests: an online genetic information resource for health care providers.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Direct reporting of laboratory test results to patients by mail to enhance patient safety.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Effects of computerized clinical decision support systems on practitioner performance and patient outcomes: a systematic review

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Genetic testing in primary care

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Genetic testing coverage and reimbursement: a provider's dilemma

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Barriers to the provision of genetic services by primary care physicians: a systematic review of the literature

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Clinically relevant breast cancer reporting: using process measures to improve anatomic pathology reporting.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Clinical laboratory reports in molecular pathology

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Synoptic reporting in tumor pathology: advantages of a web-based system

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Clinical genetics issues encountered by family physicians

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Interaction of genetic counselors with molecular genetic testing laboratories: implications for non-geneticist health care providers.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Laboratory standards and guidelines for population-based cystic fibrosis carrier screening

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2665866

Physicians' perceived usefulness of and satisfaction with test reports for cystic fibrosis (DeltaF508) and factor V Leiden

3 September 2018

1 reference

12 December 2020

Cystic fibrosis gene testing a challenge: experts say widespread use is creating unnecessary risks

1 reference

12 December 2020

The use and interpretation of commercial APC gene testing for familial adenomatous polyposis

1 reference

12 December 2020

Physician survey of a laboratory medicine interpretive service and evaluation of the influence of interpretations on laboratory test ordering

1 reference

12 December 2020

Reporting BRCA test results to primary care physicians

1 reference

12 December 2020

Clinical interpretation and recommendations for patients with a variant of uncertain significance in BRCA1 or BRCA2: a survey of genetic counseling practice

1 reference

12 December 2020

Medical genetic test reporting for cystic fibrosis (deltaF508) and factor V Leiden in North American laboratories

1 reference

12 December 2020

Impact of self-reported familiarity with guidelines for cystic fibrosis carrier screening

1 reference

12 December 2020

Technical standards and guidelines: molecular genetic testing for ultra-rare disorders

1 reference

12 December 2020

Testing and reporting ACMG cystic fibrosis mutation panel results

1 reference

12 December 2020

Key Internet genetics resources for the clinician

1 reference

12 December 2020

10.2353/JMOLDX.2009.080130

Identifiers

DOI

1 reference

18 August 2017

1 reference

18 August 2017

PubMed publication ID

19197001

1 reference