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Autor:
Alrayes N; Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.; Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Issa NM; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, Egypt., Alghubayshi OY; Saudi Arabia Ministry of Health, Khobar Hospital and Health Centers Management, Al-Khobar, Saudi Arabia., Al-Amaa JY; Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Alsabban AH; Department of Biological Science, Faculty of Sciences, King Abdulaziz University, Jeddah, Saudi Arabia., Al Shaer DS; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Alyoubi RA; Pediatric Department, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Nasser KK; Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.; Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Alkhiary YM; Oral and Maxillofacial Prosthodontics Department, Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia.
Publikováno v:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jan; Vol. 12 (1), pp. e2337. Date of Electronic Publication: 2023 Dec 13.