DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
LinksClose Window
References
Huber J, Peres VC, de Castro AL. , et al.
Molecular screening for 22Q11.2 deletion syndrome in patients with congenital heart disease.
Pediatr Cardiol 2014;
35 (08) 1356-1362
We do not assume any responsibility for the contents of the web pages of other providers.