Ge, Ruiyang; Ching, Christopher R.K.; Bassett, Anne S.; Kushan, Leila; Antshel, Kevin M.; van Amelsvoort, Therese; Bakker, Geor; Butcher, Nancy J.; Campbell, Linda E.; Chow, Eva W.C.; Craig, Michael; Crossley, Nicolas A.; Cunningham, Adam; Daly, Eileen; Doherty, Joanne L.; Durdle, Courtney A.; Emanuel, Beverly S.; Fiksinski, Ania; Forsyth, Jennifer K.; Fremont, Wanda; Goodrich-Hunsaker, Naomi J.; Gudbrandsen, Maria; Gur, Raquel E.; Jalbrzikowski, Maria; Kates, Wendy R.; Lin, Amy; Linden, David E.J.; McCabe, Kathryn L.; McDonald-McGinn, Donna; Moss, Hayley; Murphy, Declan G.; Murphy, Kieran C.; Owen, Michael J.; Villalon-Reina, Julio E.; Repetto, Gabriela M.; Roalf, David R.; Ruparel, Kosha; Schmitt, J. Eric; Schuite-Koops, Sanne; Angkustsiri, Kathleen; Sun, Daqiang; Vajdi, Ariana; van den Bree, Marianne; Vorstman, Jacob; Thompson, Paul M.; Vila-Rodriguez, Fidel; Bearden, Carrie E.
(Wiley-Liss Inc., 2024-01)
22q11.2 deletion syndrome (22q11DS) is the most frequently occurring microdeletion in humans. It is associated with a significant impact on brain structure, including prominent reductions in gray matter volume (GMV), and ...