Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity. (Q41543943)

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scientific article published on 22 January 2015

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English	Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.	scientific article published on 22 January 2015

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28 February 2020

Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity (English)

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28 February 2020

hypertrophic cardiomyopathy

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CORRIGENDUM: Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.

1 reference

10.1038/GIM.2015.16

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1038/GIM.2015.16

Melissa A Kelly

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28 February 2020

Jonathan G Seidman

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J G Seidman

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28 February 2020

Christine E. Seidman

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Christine E Seidman

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28 February 2020

Steven R DePalma

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Steven R DePalma

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Birgit H Funke

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Ahmed A Alfares

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28 February 2020

Stephanie J Cox

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Stephanie W Cox

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Gregory McDermott

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28 February 2020

Samantha B Baxter

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28 February 2020

Heather M McLaughlin

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Eugene H Clark

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28 February 2020

Larry J Babb

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22 January 2015

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28 February 2020

Genetics in Medicine

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28 February 2020

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880-888

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28 February 2020

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Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

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Hypertrophic cardiomyopathy: a systematic review

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Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era.

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Familial Wolff-Parkinson-White Syndrome: a disease of glycogen storage or ion channel dysfunction?

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Evaluation of second-generation sequencing of 19 dilated cardiomyopathy genes for clinical applications

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Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy

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A systematic approach to assessing the clinical significance of genetic variants.

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Shared genetic causes of cardiac hypertrophy in children and adults

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Alternative splicing in the alpha-galactosidase A gene: increased exon inclusion results in the Fabry cardiac phenotype

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Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy

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Enzyme assay and clinical assessment in subjects with a Chinese hotspot late-onset Fabry mutation (IVS4 + 919G→A).

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Measurement of urinary CDH and CTH by tandem mass spectrometry in patients hemizygous and heterozygous for Fabry disease

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Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic cardiomyopathy

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Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives

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Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy.

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Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy

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Communicating new knowledge on previously reported genetic variants

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DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model

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A cost-effectiveness model of genetic testing for the evaluation of families with hypertrophic cardiomyopathy

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Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

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Arrhythmogenic right ventricular cardiomyopathy/dysplasia: clinical impact of molecular genetic studies

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7 January 2021

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Prevalence of fabry disease in a cohort of 508 unrelated patients with hypertrophic cardiomyopathy

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7 January 2021

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High Incidence of the Cardiac Variant of Fabry Disease Revealed by Newborn Screening in the Taiwan Chinese Population

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7 January 2021

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The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands

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10.1038/GIM.2014.205

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28 February 2020

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28 February 2020

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