학술논문
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations
Document Type
Article
Author
Dias, K.-R.; Evans, C.-A.; Roscioli, T.; Carlston, C.M.; Blok, L.E.R.; Schenck, A.; De Hayr, L.; Harvey, R.J.; Nawaz, U.; Zhu, Y.; Kirk, E.P.; Buckley, M.F.; Bayrak-Toydemir, P.; Htun, S.; Slavotinek, A.M.; Ma, A.; Lynch, S.A.; Moorwood, C.; Stals, K.; Ellard, S.; Bainbridge, M.N.; Friedman, J.; Pappas, J.G.; Rabin, R.; Nowak, C.B.; Douglas, J.; Wilson, T.E.; Guillen Sacoto, M.J.; Mullegama, S.V.; Palculict, T.B.; Pinner, J.R.; Edwards, M.; Montanari, F.; Graziano, C.; Pippucci, T.; Dingmann, B.; Glass, I.; Mefford, H.C.; Shimoji, T.; Suzuki, T.; Yamakawa, K.; Streff, H.; Schaaf, C.P.; Voineagu, I.; Carey, J.C.
Source
In: Genetics in Medicine . (Genetics in Medicine, September 2022, 24(9):1952-1966)
Subject
Language
English
ISSN
15300366
10983600
10983600