Browsing by Author "e96e3be9-0b2e-40d2-934a-4c202ca982b6"
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León, Luis; Benavides, Felipe; Espinoza, Karena; Vial, Cecilia; Alvarez Zenteno, Patricia; Lay Son, Guillermo; Miranda, Macarena; Repetto, Gabriela (Nature, 2017)22q11.2 microdeletion syndrome (22q11.2DS) is the most common microdeletion disorder in humans, with an incidence of 1/4000 live births. It is caused by a heterozygous deletion of 1.5-3 Mb on chromosome region 22q11.2. ...