Persistent URL of this record https://hdl.handle.net/1887/3766912
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Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
- All authors
- Sobering, A.K.; Bryant, L.M.; Li, D.; McGaughran, J.; Maystadt, I.; Moortgat, S.; Graham, J.M.; Haeringen, A. van; Ruivenkamp, C.; Cuperus, R.; Vogt, J.; Morton, J.; Brasch-Andersen, C.; Steenhof, M.; Hansen, L.K.; Adler, É.; Lyonnet, S.; Pingault, V.; Sandrine, M.; Ziegler, A.; Donald, T.; Nelson, B.; Holt, B.; Petryna, O.; Firth, H.; McWalter, K.; Zyskind, J.; Telegrafi, A.; Juusola, J.; Person, R.; Bamshad, M.J.; Earl, D.; Tsai, A.C.H.; Yearwood, K.R.; Marco, E.; Nowak, C.; Douglas, J.; Hakonarson, H.; Bhoj, E.J.; Univ Washington Ctr Mendelian Geno
- Date
- 2022-04-18
- Volume
- 3
- Issue
- 3