P21.005.A CHD8 missense variants cause a variable neurodevelopmental disorder with incomplete penetrance

M Godfrey, M Levy, E Leonardi, C Campbell, L Demain, S Jenkinson, S Hilton, BA Castillo, M Balasubramanian, EK Bijlsma, E Burkitt-Wright, G Cappuccio, K Chandler, K Devriendt, M Haanpää, C Hörnig, EA Jones, S Kocagil, H Koillinen, DL NarayananR Madhu, P Majethia, A Murgia, E Rosser, M Schülke-Gerstenfeld, A Shukla, E Soengas-Gonda, Y Sznajer, MM Venancio, T Wright, D Gokhale, B Sadikovic, SD Houge, S Banka

Research output: Contribution to journalMeeting Abstractpeer-review

Original languageEnglish
Pages (from-to)721
Number of pages1
JournalEuropean Journal of Human Genetics
Volume32
Issue numberSupplement 1
Publication statusPublished - 8 Jan 2024

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