Detailed analysis of 22q11.2 with a high density MLPA probe set
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference42 articles.
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2. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population;Botto;Pediatrics,2003
3. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11;Burn;J Med Genet,1993
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