DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Brunet A, Gabau E, Perich RM. , et al.
Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.
Am J Med Genet A 2006;
140 (22) 2426-2432
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