Microdeletion 22q11 in humans causes velocardiofacial and DiGeorge syndromes. Most patients share a common 3Mb deletion, but the clinical manifestations are very heterogeneous. Congenital heart disease is present in 50-80
作者：Juan Francisco, Calderón；Alonso R, Puga；M Luisa, Guzmán；Carmen Paz, Astete；Marta, Arriaza；Mariana, Aracena；Teresa, Aravena；Patricia, Sanz；Gabriela M, Repetto
来源：Biological research 2009 年 42卷 4期
