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Page 1
Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta.
Hany U, Watson CM, Liu L, Smith CEL, Harfoush A, Poulter JA, Nikolopoulos G, Balmer R, Brown CJ, Patel A, Simmonds J, Charlton R, Acosta de Camargo MG, Rodd HD, Jafri H, Antanaviciute A, Moffat M, Al-Jawad M, Inglehearn CF, Mighell AJ. Hany U, et al. Among authors: rodd hd. J Med Genet. 2024 Mar 21;61(4):347-355. doi: 10.1136/jmg-2023-109510. J Med Genet. 2024. PMID: 37979963 Free PMC article.
An International Investigation of Molar Incisor Hypomineralisation (iMIH) and Its Association with Dental Anomalies: Development of a Protocol.
Rodd HD, Nazzal H, Bonifacio CC, Ruth CW, Crombie F, El Shahawy O, Folayan MO, Gambetta-Tessini K, Goyal A, Hasmun N, Issa AI, Jundi S, Manton DJ, Narasimhan S, Omar S, Parekh S, Popoola BO, Silva M, Taylor G, Naomi YQ. Rodd HD, et al. Dent J (Basel). 2023 Apr 28;11(5):117. doi: 10.3390/dj11050117. Dent J (Basel). 2023. PMID: 37232768 Free PMC article.
41 results