Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome.

Authors

Gelila Yitsege, George Washington University
Bethany A Stokes
Julia A. Sabatino, George Washington University
Kelsey F Sugrue
Gabor Banyai, George Washington University
Elizabeth M. Paronett, George Washington University
Beverly A. Karpinski, George Washington University
Thomas M. Maynard, George Washington University
Anthony S. LaMantia, George Washington University
Irene E. Zohn, George Washington University

Document Type

Journal Article

Publication Date

5-20-2020

Journal

Birth Defects Research

DOI

10.1002/bdr2.1709

Comments

Online ahead of print

APA Citation

Yitsege, G., Stokes, B., Sabatino, J. A., Sugrue, K., Banyai, G., Paronett, E. M., Karpinski, B. A., Maynard, T. M., LaMantia, A. S., & Zohn, I. E. (2020). Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome.. Birth Defects Research, (). http://dx.doi.org/10.1002/bdr2.1709