Items where authors include "Robson, EA"
Article
Robson, EA, Dixon, L, Causon, L et al. (12 more authors) (2020) Hydrocephalus and diffuse choroid plexus hyperplasia in primary ciliary dyskinesia-related MCIDAS mutation. Neurology Genetics, 6 (4). e482. ISSN 2376-7839
Shoemark, A, Moya, E, Hirst, RA et al. (34 more authors) (2018) High prevalence of CCDC103 p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigations. Thorax, 73 (2). pp. 157-166. ISSN 0040-6376
Robson, EA, Chetcuti, P, Hirst, RA et al. (6 more authors) (2017) Update on primary ciliary dyskinesia. Paediatrics and Child Health, 27 (7). pp. 337-342. ISSN 1751-7222