학술논문
Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt
Document Type
Article
Author
Shepherdson, J.L.; Hutchison, K.; Nicolet, C.M.; Farnham, P.J.; Don, D.W.; Choi, T.-I.; Kim, C.-H.; McGillivray, G.; White, S.M.; Amor, D.J.; Lockhart, P.; Pope, K.; Allan, C.A.; Banka, S.; Jackson, A.; Basel, D.G.; McCarrier, J.; Buch, L.D.; Stolerman, E.; Carere, D.A.; Schnur, R.E.; Carroll, R.; Shaw, M.; Corbett, M.A.; Gecz, J.; Clayton-Smith, J.; Crawford, A.; Taylor, J.P.; Dunø, M.; Østergaard, E.; Faivre, L.; Maraval, J.; Gilfillan, C.P.; McCarthy, J.; Gold, N.B.; Gripp, K.W.; Wadman, E.; Hobson, E.; Amel Riazat Kesh, L.; Holtz, A.M.; Innes, A.M.; Isidor, B.; Küry, S.; Katsonis, P.; Posey, J.E.; Lupski, J.R.; Lichtarge, O.; Lecoquierre, F.; Matsumoto, N.; Miyake, N.; Moey, L.H.; Németh, A.H.; Patel, R.; Wakeling, E.; Wong, L.C.; Shinawi, M.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 7 March 2024, 111(3):487-508)
Subject
Language
English
ISSN
15376605
00029297
00029297