Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.

Heart (British Cardiac Society) - 1 Aug 1997

Burn J, Camm J, Davies M J, Peltonen L, Schwartz P J, Watkins H

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cardiomyopathy, Hypertrophic
Share to Genes, Dominant
Share to Genetic Testing
Share to Genotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Long QT Syndrome

Share to Marfan Syndrome

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 9326982
DOI: 10.1136/hrt.78.2.110
PMCID: PMC484888

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.PMID 9326982Read ↗

Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases:hypertrophic cardiomyopathy, long-QT syndrome, and Marfan syndrome. A statement for healthcare professionals from the Councils on Clinical Cardiology, Cardiovascular Disease in the Young, and Basic Science, American Heart Association.Semantic proximity Read ↗

Clinical Challenges of Genotype Positive (+)–Phenotype Negative (−) Family Members in Hypertrophic CardiomyopathySemantic proximity Read ↗

Genetic characterization and genotype-phenotype associations in a large cohort of patients with hypertrophic cardiomyopathy – An ancillary study of the Portuguese registry of hypertrophic cardiomyopathySemantic proximity Read ↗

Phenotype (ECG)-genotype considerations in long QT syndrome and Brugada syndrome.Semantic proximity Read ↗

Molecular genetics of inherited long QT syndromes.Semantic proximity Read ↗

Genotype-phenotype relationships in congenital long QT syndrome.Semantic proximity Read ↗

The long QT syndrome and catecholaminergic polymorphic ventricular tachycardia.Semantic proximity Read ↗

Genotype-phenotype correlation in congenital heart disease.Semantic proximity Read ↗

Long-QT syndrome: from genetics to management.Semantic proximity Read ↗

Short QT and dilated cardiomyopathy. A phenotype with a good prognosis?Semantic proximity Read ↗

Genotype-phenotype correlations in Polish patients with hypertrophic cardiomyopathy: Preliminary report.Semantic proximity Read ↗

Genetic testing and cascade screening in pediatric long QT syndrome and hypertrophic cardiomyopathySemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.