Items where authors include "DeVile, C."

Article

Thornley, P., Bishop, N. orcid.org/0000-0001-7263-8546, Baker, D. et al. (10 more authors) (2022) Non-collagen pathogenic variants resulting in the osteogenesis imperfecta phenotype in children: a single-country observational cohort study. Archives of Disease in Childhood, 107 (5). pp. 486-490. ISSN 0003-9888

Durkin, A., DeVile, C., Arundel, P. et al. (11 more authors) (2021) Expanding the phenotype of SPARC-related osteogenesis imperfecta : clinical findings in two patients with pathogenic variants in SPARC and literature review. Journal of Medical Genetics. ISSN 0022-2593

Sadleir, L.G., Mountier, E.I., Gill, D. et al. (13 more authors) (2017) Not all SCN1A epileptic encephalopathies are Dravet syndrome. Neurology, 89 (10). pp. 1035-1042. ISSN 0028-3878

Balasubramanian, M. orcid.org/0000-0003-1488-3695, Hurst, J., Brown, S. et al. (16 more authors) (2016) Compound heterozygous variants in NBAS as a cause of atypical osteogenesis imperfecta. Bone, 94. pp. 65-74. ISSN 8756-3282

Proceedings Paper

Balasubramanian, M., Hurst, J., DeVile, C. et al. (8 more authors) (2017) NBAS variants causing a novel form of inherited bone fragility. In: Bone Abstracts. 8th International Conference on Children's Bone Health , 10-13 Jun 2017, Wurzburg, Germany. Bioscientifica , Bristol, UK .