Diagnosis of 22q11.2 deletion syndrome in children with congenital heart diseases and facial dysmorphisms-Reference-Cited by-同舟云学术

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Diagnosis of 22q11.2 deletion syndrome in children with congenital heart diseases and facial dysmorphisms

Published:2022-08 Issue: Volume: Page:
ISSN:0377-1237
Container-title:Medical Journal Armed Forces India
language:en
Short-container-title:Medical Journal Armed Forces India

Author:

Agarwal Manisha,Kumar Vivek,Dwivedi Aradhana

Publisher

Elsevier BV

Subject

General Medicine

Reference23 articles.

1. What is new in genetics of congenital heart defects?;Digilio;Front Pediatr,2016

2. Genetic Syndromes associated with congenital heart disease;Ko;Korean Circ J,2015

3. Birth prevalence of congenital heart disease worldwide;van der Linde;J Am Coll Cardiol,2011

4. The incidence of congenital heart disease;Hoffman;J Am Coll Cardiol,2002

5. Epidemiology of congenital heart disease in India;Dixit;Congenit Heart Dis,2015

Cited by 1 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. Conotruncal Heart Defects: A Narrative Review of Molecular Genetics, Genomics Research and Innovation;OMICS: A Journal of Integrative Biology;2024-07-01

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