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Ophthalmic Genetics|August 20, 2013
Partial duplication of chromosome 19 associated with syndromic duane retraction syndromeKhaled K Abu-Amero, Altaf A Kondkar, Abdullah Al Otaibi, et al.American Journal of Medical Genetics. Part A|April 17, 2008
The clinical spectrum of homozygous HOXA1 mutationsThomas M Bosley, Ibrahim A Alorainy, Mustafa A Salih, et al.Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|December 15, 2010
Congenital myasthenic syndrome due to homozygous CHRNE mutations: report of patients in ArabiaMustafa A Salih, Darren T Oystreck, Yasser H Al-Faky, et al.Ophthalmic Genetics|February 15, 2013
Ophthalmologic observations in a patient with partial mosaic trisomy 8Khaled K Abu-Amero, Altaf A Kondkar, Mustafa A Salih, et al.American Journal of Medical Genetics. Part A|May 2, 2013
A newly recognized autosomal recessive syndrome affecting neurologic function and visionMustafa A Salih, Andreas Tzschach, Darren T Oystreck, et al.Saudi Medical Journal|April 22, 2014
Ocular malignant tumors. Review of the Tumor Registry at a tertiary eye hospital in central Saudi ArabiaRajiv B Khandekar, Abdulelah A Al-Towerki, Hind Al-Katan, et al.BMC Medical Genetics|February 26, 2011
Molecular and neurological characterizations of three Saudi families with lipoid proteinosisMustafa A Salih, Khaled K Abu-Amero, Saleh Alrasheed, et al.Nature Genetics|September 13, 2005
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive developmentMax A Tischfield, Thomas M Bosley, Mustafa A M Salih, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 24, 2015
Mutation in GM2A Leads to a Progressive Chorea-dementia SyndromeMustafa A Salih, Mohammed Z Seidahmed, Heba Y El Khashab, et al.Retinal Cases & Brief Reports|March 16, 2017
NEW OBSERVATIONS REGARDING THE RETINOPATHY OF GENETICALLY CONFIRMED KEARNS-SAYRE SYNDROMEIgor Kozak, Darren T Oystreck, Khaled K Abu-Amero, et al.Pageof 12