Items where authors include "White, S.M."

Article

Chen, Y. orcid.org/0000-0001-5593-6920, Dawes, R. orcid.org/0000-0003-2135-0117, Kim, H.C. orcid.org/0000-0001-5877-5456 et al. (116 more authors) (2024) De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature, 632. pp. 832-840. ISSN 0028-0836

Balasubramanian, M. orcid.org/0000-0003-1488-3695, Dingemans, A.J.M., Albaba, S. et al. (36 more authors) (2021) Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype. European Journal of Human Genetics, 29 (4). pp. 625-636. ISSN 1018-4813

Myers, K.A., White, S.M., Mohammed, S. et al. (6 more authors) (2018) Corrigendum to "Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome" [Epilepsy Res. 140 (2018) 166-170]. Epilepsy Research, 147. p. 121. ISSN 0920-1211

Myers, K.A., White, S.M., Mohammed, S. et al. (6 more authors) (2018) Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome. Epilepsy Research, 140. pp. 166-170. ISSN 0920-1211