Items where authors include "Black, G.C."

Article

Smith, C.E.L. orcid.org/0000-0001-8320-5105, Laugel-Haushalter, V., Hany, U. orcid.org/0000-0002-4486-1625 et al. (15 more authors) (2024) Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability. Journal of Medical Genetics. ISSN 0022-2593

Julian, T.H., Girach, Z., Sanderson, E. et al. (5 more authors) (2023) Causal factors in primary open angle glaucoma: a phenome-wide Mendelian randomisation study. Scientific Reports, 13. 9984. ISSN 2045-2322