Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome

por Paronett, Elizabeth M, Bryan, Corey A, Maynard, Megan E, Goroff, Julia A, Meechan, Daniel W, LaMantia, Anthony-Samuel, Maynard, Thomas M
Publicado 2023

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

por Yitsege, Gelila, Stokes, Bethany A., Sabatino, Julia A., Sugrue, Kelsey F., Banyai, Gabor, Paronett, Elizabeth M., Karpinski, Beverly A., Maynard, Thomas M., LaMantia, Anthony‐S., Zohn, Irene E.
Publicado 2020