Items where authors include "Keigwin, S."

Article

Vilaca, T. orcid.org/0000-0002-9227-6076, Gossiel, F., Delaney, S. et al. (4 more authors) (2025) Family mapping of previously identified patients with pathogenic or likely pathogenic ALPL variants using predictive genotyping and detailed phenotyping approach: the FAME case-control study. JBMR Plus, 9 (5). ziaf034. ISSN 2473-4039

Bowen, J.M. orcid.org/0000-0002-3292-2582, Hernandez, M. orcid.org/0000-0003-4474-5883, Johnson, D.S. et al. (9 more authors) (2023) Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield. European Journal of Human Genetics, 31 (7). pp. 749-760. ISSN 1018-4813

Campanini, E.H., Baker, D., Arundel, P. et al. (9 more authors) (2021) High bone mass phenotype in a cohort of patients with Osteogenesis Imperfecta caused due to BMP1 and C-propeptide cleavage variants in COL1A1. Bone Reports, 15. 101102.