Congenital heart defects associated with aneuploidy syndromes: New insights into familiar associations
Author:
Affiliation:
1. Medical Genetics Unit, Department of PediatricsMassGeneral Hospital for Children Boston Massachusetts
2. Division of Pediatric EndocrinologyCincinnati Children's Hospital Medical Center Cincinnati Ohio
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.c.31760
Reference95 articles.
1. Trisomy 22 Mosaicism and Normal Developmental Outcome: Report of Two Patients and Review of the Literature
2. Targeted Next-Generation Sequencing of 406 Genes Identified Genetic Defects Underlying Congenital Heart Disease in Down Syndrome Patients
3. Clinical and molecular studies in full trisomy 22: Further delineation of the phenotype and review of the literature
4. Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study
5. Congenital polyvalvular disease in trisomy 18: Echocardiographic diagnosis
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