Items where authors include "Moffat, M."

Article

Hany, U., Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (16 more authors) (2025) Genetic Screening of a Nonsyndromic Amelogenesis Imperfecta Patient Cohort Using a Custom smMIP Reagent for Selective Enrichment of Target Loci. Human Mutation, 2025. 8942542. ISSN 1059-7794

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. orcid.org/0009-0008-3593-8409 et al. (16 more authors) (2025) Genetic Screening of a nonsyndromic amelogenesis imperfecta patient cohort using a custom smMIP reagent for selective enrichment of target loci. Human Mutation, 2025 (1). 8942542. ISSN 1059-7794

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (17 more authors) (2024) Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta. Journal of Medical Genetics, 61 (4). pp. 347-355. ISSN 0022-2593

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (17 more authors) (2024) Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta. Journal of Medical Genetics, 61 (4). pp. 347-355. ISSN 0022-2593

Hughes, S., Balmer, R., Moffat, M. et al. (1 more author) (2019) The dental management of children with congenital heart disease following the publication of Paediatric Congenital Heart Disease Standards and Specifications. British Dental Journal (BDJ), 226 (6). pp. 447-452. ISSN 0007-0610