Items where authors include "Anderson, G."

Article

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

Levan, A. orcid.org/0000-0001-7821-9369, Gompertz, B.P. orcid.org/0000-0002-5826-0548, Salafia, O.S. et al. (82 more authors) (2024) Heavy element production in a compact object merger observed by JWST. Nature, 626 (8000). pp. 737-741. ISSN 0028-0836

Buonocore, F., Kuehnen, P., Suntharalingham, J.P. et al. (24 more authors) (2017) Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans. JOURNAL OF CLINICAL INVESTIGATION, 127 (5). pp. 1700-1713. ISSN 0021-9738