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A single-centre study of genetic mutations, audiology, echocardiogram and pulmonary function in Saudi children with osteogenesis imperfecta.
Ahmad N, Aleysae NA, Sobaihi M, Naitah N, Rasol MA, Al-Kouatli AA, Almaghamsi TM, Heaphy ELG, Attiyah MH, Hrays M, Alghamdi B, Alzahrani AS. Ahmad N, et al. Among authors: alghamdi b. J Pediatr Endocrinol Metab. 2021 Dec 23;35(3):355-362. doi: 10.1515/jpem-2021-0587. Print 2022 Mar 28. J Pediatr Endocrinol Metab. 2021. PMID: 34954934
Molecular Genetics of Diffuse Sclerosing Papillary Thyroid Cancer.
Alswailem M, Alghamdi B, Alotaibi A, Aljomiah A, Al-Hindi H, Murugan AK, Abouelhoda M, Shi Y, Alzahrani AS. Alswailem M, et al. Among authors: alghamdi b. J Clin Endocrinol Metab. 2023 Aug 18;108(9):e704-e711. doi: 10.1210/clinem/dgad185. J Clin Endocrinol Metab. 2023. PMID: 36995892
225 results