(Q37133904)

18 August 2017

1 reference

title

Genetic testing and genetic counseling in cardiovascular genetic medicine: overview and preliminary recommendations (English)

1 reference

18 August 2017

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Jason Cowan

1

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18 August 2017

Ana Morales

series ordinal

2

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18 August 2017

Jimena Dagua

series ordinal

3

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18 August 2017

Ray E Hershberger

series ordinal

4

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18 August 2017

publication date

1 March 2008

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18 August 2017

published in

Congestive Heart Failure

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18 August 2017

volume

14

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18 August 2017

issue

2

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18 August 2017

page(s)

97-105

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DNA analysis: what and when to request?

18 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Genetic testing in cardiovascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Genetic test evaluation: information needs of clinicians, policy makers, and the public

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Clinical and genetic issues in familial dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Genes, calcium and modifying factors in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Genetic testing for risk stratification in hypertrophic cardiomyopathy and long QT syndrome: fact or fiction?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Inherited arrhythmogenic diseases: the complexity beyond monogenic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the Euro

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

The complete sequence of the human beta-myosin heavy chain gene and a comparative analysis of its product

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Policy implications of genetic testing: not just for geneticists anymore

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Genetic nondiscrimination.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Integrating molecular medicine into the US health-care system: opportunities, barriers, and policy challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

ASHG Statement* on Direct-to-Consumer Genetic Testing in the United States

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Clinical genetics in cardiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Genetics of hypertrophic cardiomyopathy: one, two, or more diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08217.X

10.1111/J.1751-7133.2008.08217.X

21 January 2018

Identifiers

DOI

1 reference

release_hui32q4qanhlxchu65xvmgq4zq

18 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/hui32q4qanhlxchu65xvmgq4zq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference