Items where authors include "Hambleton, S."

Article

Cipriani, V. orcid.org/0000-0002-0839-9955, Vestito, L. orcid.org/0000-0003-0008-936X, Magavern, E.F. orcid.org/0000-0003-0699-6411 et al. (58 more authors) (2025) Rare disease gene association discovery in the 100,000 Genomes Project. Nature. ISSN 0028-0836

Chen, R. orcid.org/0000-0003-2887-2751, Lukianova, E. orcid.org/0000-0003-3566-5873, van der Loeff, I.S. orcid.org/0000-0003-1196-6196 et al. (34 more authors) (2024) NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome. Science Immunology, 9 (95). eade5705. ISSN 2470-9468

Hägele, P., Staus, P., Scheible, R. et al. (146 more authors) (2024) Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study. The Lancet Haematology, 11 (2). e114-e126. ISSN 2451-9960

Cheetham, T.D., Cole, M., Abinun, M. et al. (15 more authors) (2022) Adjuvant rituximab—exploratory trial in young people with Graves disease. The Journal of Clinical Endocrinology & Metabolism, 107 (3). pp. 743-754. ISSN 0021-972X