Guillen Sacoto, Maria J.
Tchasovnikarova, Iva A.
Torti, Erin
Forster, Cara
Andrew, E. Hallie
Anselm, Irina
Baranano, Kristin W.
Briere, Lauren C.
Cohen, Julie S.
Craigen, William J.
Cytrynbaum, Cheryl
Ekhilevitch, Nina
Elrick, Matthew J.
Fatemi, Ali
Fraser, Jamie L.
Gallagher, Renata C.
Guerin, Andrea
Haynes, Devon
High, Frances A.
Inglese, Cara N.
Kiss, Courtney
Koenig, Mary Kay
Krier, Joel
Lindstrom, Kristin
Marble, Michael
Meddaugh, Hannah
Moran, Ellen S.
Morel, Chantal F.
Mu, Weiyi
Muller, Eric A. II
Nance, Jessica
Natowicz, Marvin R.
Numis, Adam L.
Ostrem, Bridget
Pappas, John
Stafstrom, Carl E.
Streff, Haley
Sweetser, David A.
Szybowska, Marta
Walker, Melissa A.
Wang, Wei
Weiss, Karin
Weksberg, Rosanna
Wheeler, Patricia G.
Yoon, Grace
Kingston, Robert E.
Juusola, Jane
Funding for this research was provided by:
Common Fund
This article is maintained by: Elsevier
Article Title: De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism
Journal Title: The American Journal of Human Genetics
CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.ajhg.2020.06.013
Content Type: article
Copyright: © 2020 American Society of Human Genetics.