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Middle East African Journal of Ophthalmology|May 17, 2011
Schnyder Corneal Dystrophy in a Saudi Arabian Family with Heterozygous UBIAD1 Mutation (p.L121F)Huda Al-Ghadeer, Jawahir Y Mohamed, Arif O KhanJournal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|November 12, 2013
Corneal enlargement without optic disk cupping in children with recessive CYP1B1 mutationsArif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, et al.Ophthalmic Genetics|January 11, 2012
Phenotype-genotype correlation in potential female carriers of X-linked developmental cataract (Nance-Horan syndrome)Arif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|February 1, 2013
Congenital glaucoma with acquired peripheral circumferential iris degenerationArif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, et al.The British Journal of Ophthalmology|January 24, 2012
Clinical and molecular analysis of children with central pulverulent cataract from the Arabian PeninsulaArif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|November 20, 2012
CYP1B1 analysis of unilateral primary newborn glaucoma in Saudi childrenArif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|May 21, 2011
Familial juvenile glaucoma with underlying homozygous p.G61E CYP1B1 mutationsArif O Khan, Lama Al-Abdi, Jawahir Y Mohamed, et al.The British Journal of Ophthalmology|March 9, 2012
The distinct ophthalmic phenotype of Knobloch syndrome in childrenArif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, et al.Human Mutation|March 15, 2012
Identification of a truncation mutation of acylglycerol kinase (AGK) gene in a novel autosomal recessive cataract locusMohammed A Aldahmesh, Arif O Khan, Jawahir Y Mohamed, et al.American Journal of Human Genetics|January 8, 2013
Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomalyJawahir Y Mohamed, Eissa Faqeih, Abdulmonem Alsiddiky, et al.Pageof 3