A single-centre study of genetic mutations, audiology, echocardiogram and pulmonary function in Saudi children with osteogenesis imperfecta.

Autor: Ahmad N; King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia., Aleysae NA; King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia., Sobaihi M; King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia., Naitah N; King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia., Rasol MA; King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia., Al-Kouatli AA; King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia., Almaghamsi TM; King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia., Heaphy ELG; Research Centre, King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia., Attiyah MH; King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia., Hrays M; King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia., Alghamdi B; Molecular Oncology Department, King Faisal Specialist Hospital & Research Centre (Gen. Org.), Riyadh, Saudi Arabia., Alzahrani AS; Research Centre, King Faisal Specialist Hospital & Research Centre (Gen. Org.), Jeddah, Saudi Arabia.

Publikováno v: Journal of pediatric endocrinology & metabolism : JPEM [J Pediatr Endocrinol Metab] 2021 Dec 23; Vol. 35 (3), pp. 355-362. Date of Electronic Publication: 2021 Dec 23 (Print Publication: 2022).