Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.

MLA

Meechan, Daniel W., et al. “Diminished Dosage of 22q11 Genes Disrupts Neurogenesis and Cortical Development in a Mouse Model of 22q11 Deletion/DiGeorge Syndrome.” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 38, Sept. 2009, pp. 16434–45. EBSCOhost, https://doi.org/10.1073/pnas.0905696106.

APA

Meechan, D. W., Tucker, E. S., Maynard, T. M., & LaMantia, A.-S. (2009). Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome. Proceedings of the National Academy of Sciences of the United States of America, 106(38), 16434–16445. https://doi.org/10.1073/pnas.0905696106

Chicago

Meechan, Daniel W, Eric S Tucker, Thomas M Maynard, and Anthony-Samuel LaMantia. 2009. “Diminished Dosage of 22q11 Genes Disrupts Neurogenesis and Cortical Development in a Mouse Model of 22q11 Deletion/DiGeorge Syndrome.” Proceedings of the National Academy of Sciences of the United States of America 106 (38): 16434–45. doi:10.1073/pnas.0905696106.