Open AccessDiminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome
Author(s) -
D. W. Meechan,
E. S. Tucker,
T. M. Maynard,
A.-S. LaMantia
Publication year - 2009
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/hvw0-sx97
Subject(s) - digeorge syndrome , neurogenesis , deletion syndrome , gene , biology , genetics , phenotype