Items where authors include "Gale, T"

Article

Taylor, RL, Soriano, CS, Williams, S et al. (9 more authors) (2022) Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia. Orphanet Journal of Rare Diseases, 17. 110. ISSN 1750-1172

Aslet, M.E.D, Paton, Lewis William orcid.org/0000-0002-3328-5634, Gale, T et al. (1 more author) (2020) Evaluating the recruitment process into UK anaesthesia core training: doctors’ performance at selection and subsequent postgraduate training- a national data linkage study : a national data linkage study of doctors' performance at selection and subsequent postgraduate training. Postgraduate medical journal. pp. 14-20. ISSN 0032-5473