Items where authors include "Hammer, T.B."

Article

Elkhateeb, N. orcid.org/0000-0002-3076-3178, Crookes, R., Spiller, M. et al. (68 more authors) (2025) Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorder. Genetics in Medicine, 27 (3). 101348. ISSN 1098-3600

Cetica, V. orcid.org/0000-0001-8549-4158, Pisano, T. orcid.org/0000-0001-8920-9078, Lesca, G. orcid.org/0000-0001-7691-9492 et al. (31 more authors) (2024) Clinical and molecular characterization of patients with YWHAG‐related epilepsy. Epilepsia, 65 (5). pp. 1439-1450. ISSN 0013-9580

Yates, T.M., Suri, M., Desurkar, A. et al. (8 more authors) (2018) SLC35A2-related congenital disorder of glycosylation: Defining the phenotype. European Journal of Paediatric Neurology, 22 (6). pp. 1095-1102. ISSN 1090-3798