Abnormal spirometry in adults with 22q11.2 microdeletion and congenital heart disease
Author:
Funder
Canadian Institutes of Health Research
Publisher
Elsevier BV
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Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Clinically Relevant Genetic Considerations for Patients With Tetralogy of Fallot;CJC Pediatric and Congenital Heart Disease;2023-12
2. Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome;Genetics in Medicine;2023-03
3. Establishing the diagnosis of 22q11.2 microdeletion syndrome in congenital heart disease is now an imperative;International Journal of Cardiology Congenital Heart Disease;2021-03
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