Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference39 articles.
1. Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients;Thienpont;Eur Heart J,2007
2. Cryptic chromosomal abnormalities identified in children with congenital heart disease;Richards;Pediatr Res,2008
3. Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects;Breckpot;J Pediatr,2010
4. Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies;Goldmuntz;Congenit Heart Dis,2011
5. Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities;Lalani;Eur J Hum Genet,2013
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1. Diagnostic yield after next-generation sequencing in pediatric cardiovascular disease;Human Genetics and Genomics Advances;2024-07
2. Clinical Genetic and Genomic Testing in Congenital Heart Disease and Cardiomyopathy;Journal of Clinical Medicine;2024-04-26
3. Clinical Decision Analysis of Genetic Evaluation and Testing in 1013 Intensive Care Unit Infants with Congenital Heart Defects Supports Universal Genetic Testing;Genes;2024-04-18
4. Genomic testing and molecular diagnosis among infants with congenital heart disease in the neonatal intensive care unit;Journal of Perinatology;2024-03-18
5. Clinically Relevant Genetic Considerations for Patients With Tetralogy of Fallot;CJC Pediatric and Congenital Heart Disease;2023-12
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