Items where authors include "Shillington, A."

Article

Shafiq, T., Feng, J.L., Phillips, L. et al. (28 more authors) (2024) An expansion of the phenotype in individuals with SYNCRIP-related neurodevelopmental disorder. Rare, 2. 100052. ISSN 2950-0087

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