학술논문
De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features
Document Type
Article
Author
Burrage, Lindsay C.; Heaney, Jason D.; Kim, Seon-Young; Lanza, Denise G.; Liu, Zhandong; Mao, Dongxue; Milosavljevic, Aleksander; Nagamani, Sandesh C.S.; Posey, Jennifer E.; Ramamurthy, Uma; Ramanathan, Vivek; Rogers, Jeffrey; Rosenfeld, Jill A.; Roth, Matthew; Zahedi Darshoori, Ramin; Pan, Xueyang; Tao, Alice M.; Lu, Shenzhao; Ma, Mengqi; Hannan, Shabab B.; Slaugh, Rachel; Drewes Williams, Sarah; O'Grady, Lauren; Kanca, Oguz; Person, Richard; Carter, Melissa T.; Platzer, Konrad; Schnabel, Franziska; Abou Jamra, Rami; Roberts, Amy E.; Newburger, Jane W.; Revah-Politi, Anya; Granadillo, Jorge L.; Stegmann, Alexander P.A.; Sinnema, Margje; Accogli, Andrea; Salpietro, Vincenzo; Capra, Valeria; Ghaloul-Gonzalez, Lina; Brueckner, Martina; Simon, Marleen E.H.; Sweetser, David A.; Glinton, Kevin E.; Kirk, Susan E.; Wangler, Michael F.; Yamamoto, Shinya; Chung, Wendy K.; Bellen, Hugo J.
Source
In The American Journal of Human Genetics 4 April 2024 111(4):742-760
Subject
Language
ISSN
0002-9297