22q11.2 deletion syndrome and congenital heart disease-Reference-Cited by-同舟云学术

22q11.2 deletion syndrome and congenital heart disease

Published:2020-02-12 Issue:1 Volume:184 Page:64-72
ISSN:1552-4868
Container-title:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
language:en
Short-container-title:Am J Med Genet

Author:

Goldmuntz Elizabeth¹^ORCID

Affiliation:

1. Division of Cardiology, Children's Hospital of Philadelphia, Department of PediatricsThe Perelman School of Medicine, The University of Pennsylvania Philadelphia Pennsylvania

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.c.31774

Reference82 articles.

1. Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review

2. The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population-based study

3. The Impact of 22q11.2 Deletion Syndrome on Surgical Repair Outcomes of Conotruncal Cardiac Anomalies

4. Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome

5. Conotruncal heart defects: impact of genetic syndromes on immediate operative mortality;Anaclerio S.;Italian Heart Journal,2004

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