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

Use of Clinical Exome Sequencing in Isolated Congenital Heart Disease.

Circulation. Cardiovascular genetics - 1 Jun 2017

Zahavich Laura, Bowdin Sarah, Mital Seema

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 Exome
Share to Exome Sequencing
Share to Fatal Outcome
Share to Heart Defects, Congenital

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pregnancy

Share to Protein Domains

Share to Receptor, Notch1

Share to Sequence Deletion

Source

Identifiers

PMID: 28473349
DOI: 10.1161/CIRCGENETICS.116.001581

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Use of Clinical Exome Sequencing in Isolated Congenital Heart Disease.PMID 28473349Read ↗

Clinical utility of exome sequencing in infantile heart failureSemantic proximity Read ↗

Exploring the Mutational Landscape of Isolated Congenital Heart Defects: An Exome Sequencing Study Using Cardiac DNA.Semantic proximity Read ↗

In-Depth Genomic Analysis: The New Challenge in Congenital Heart DiseaseSemantic proximity Read ↗

Evaluation of Exome and Genome Sequencing for Critically Ill Pediatric Cardiac PatientsSemantic proximity Read ↗

In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease.Semantic proximity Read ↗

Identification of clinically actionable variants from genome sequencing of families with congenital heart diseaseSemantic proximity Read ↗

Recent advances in congenital heart disease genomicsSemantic proximity Read ↗

Application of high-throughput sequencing for studying genomic variations in congenital heart disease.Semantic proximity Read ↗

Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditionsSemantic proximity Read ↗

Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome studySemantic proximity Read ↗

Diagnostic yield after next-generation sequencing in pediatric cardiovascular disease.Semantic proximity Read ↗

Diagnostic Yield of Exome Sequencing in Pediatric CardiomyopathySemantic proximity Read ↗

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