Items where authors include "Callewaert, B."

Article

Oates, S., Absoud, M., Goyal, S. et al. (32 more authors) (2021) ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder. Clinical Genetics, 100 (4). pp. 412-429. ISSN 0009-9163

Yates, T.M., Drucker, M., Barnicoat, A. et al. (19 more authors) (2020) ZMYND11‐related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum. Human Mutation, 41 (5). pp. 1042-1050. ISSN 1059-7794

Zarate, Y.A. orcid.org/0000-0001-8235-6200, Bosanko, K.A., Caffrey, A.R. et al. (45 more authors) (2019) Mutation update for the SATB2 gene. Human Mutation, 40 (8). pp. 1013-1029. ISSN 1059-7794