DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Belangero SI, Bellucco FT, Kulikowski LD, Christofolini DM, Cernach MC, Melaragno MI.
22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype.
Arq Bras Cardiol 2009;
92 (04) 307-311
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