Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome. [electronic resource]
- The American journal of cardiology Jun 2010
- 1617-24 p. digital
Publication Type: Journal Article; Review
1879-1913
10.1016/j.amjcard.2010.01.333 doi
Adaptor Proteins, Signal Transducing--genetics Biomarkers--metabolism DiGeorge Syndrome--genetics Heart Defects, Congenital--genetics Humans Nuclear Proteins--genetics Prevalence Proto-Oncogene Protein c-ets-2--genetics T-Box Domain Proteins--genetics