Chromosome 22q11.2 duplication is rare in a population-based cohort of Danish children with cardiovascular malformations
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference28 articles.
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4. Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome;Brunet;Am J Med Genet A,2006
5. Incidence of microduplication 22q11.2 in patients referred for FISH testing for velo cardiofacial and DiGeorge syndromes;Cotter;Eur J Hum Genet,2005
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3. Copy number variation ofGATA4andNKX2-5in Chinese fetuses with congenital heart disease;Pediatrics International;2014-12-11
4. Children's Oncology Group's 2013 blueprint for research: Epidemiology;Pediatric Blood & Cancer;2012-12-19
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