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Pediatric Neurology|August 8, 2013
Autism spectrum disorders and inborn errors of metabolism: an updateMohammad Ghaziuddin, Mohammed Al-OwainEuropean Journal of Medical Genetics|October 16, 2019
Inherited Metabolic Disorders in Adults: A view from Saudi ArabiaRaashda A Sulaiman, Mohammed Al-OwainAmerican Journal of Medical Genetics. Part A|August 21, 2012
Map of autosomal recessive genetic disorders in Saudi Arabia: concepts and future directionsMohammed Al-Owain, Hamad Al-Zaidan, Zuhair Al-HassnanMolecular Vision|February 17, 2010
A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotypeMohammed A Aldahmesh, Mohammed Al-Owain, Faisal Alqahtani, et al.Orphanet Journal of Rare Diseases|April 20, 2010
A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a case reportMohammed Al-Owain, Sarar Mohamed, Namik Kaya, et al.Gene|September 27, 2012
Identification of a novel ZNF469 mutation in a large family with Ehlers-Danlos phenotypeMohammed Al-Owain, Mohammed S Al-Dosari, Asma Sunker, et al.European Journal of Pediatrics|December 30, 2009
Munchausen syndrome by proxy mimicking as Gaucher diseaseMohammed Al-Owain, Hamad Al-Zaidan, Amal Al-Hashem, et al.BMC Endocrine Disorders|March 18, 2017
Two novel LHX3 mutations in patients with combined pituitary hormone deficiency including cervical rigidity and sensorineural hearing lossKhushnooda Ramzan, Bassam Bin-Abbas, Lolwa Al-Jomaa, et al.European Journal of Pediatrics|September 25, 2010
Dyggve-Melchior-Clausen syndrome: novel splice mutation with atlanto-axial subluxationOla Khalifa, Faiqa Imtiaz, Nadia Al-Sakati, et al.Journal of Child Neurology|July 5, 2007
Muscle phosphofructokinase deficiency with neonatal seizures and nonprogressive courseZuhair N Al-Hassnan, Mustafa Al Budhaim, Mohammed Al-Owain, et al.Pageof 9