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Ophthalmic Genetics|June 18, 2013
Childhood cone-rod dystrophy with macular cystic degeneration from recessive CRB1 mutationArif O Khan, Mohammed A Aldahmesh, Leen Abu-Safieh, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 10, 2010
Helicoid subretinal fibrosis associated with a novel recessive NR2E3 mutation p.S44XArif O Khan, Mohammed A Aldahmesh, Essam Al-Harthi, et al.
Journal 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.
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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2012
Homozygous null mutation in ODZ3 causes microphthalmia in humansMohammed A Aldahmesh, Jawahir Y Mohammed, Selwa Al-Hazzaa, et al.
Molecular 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.
Ophthalmic Genetics|September 5, 2013
Lens subluxation and retinal dysfunction in a girl with homozygous VSX2 mutationArif O Khan, Mohammed A Aldahmesh, Jawaher Noor, 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.
Human Molecular Genetics|February 2, 2011
Functional analysis of BBS3 A89V that results in non-syndromic retinal degenerationPamela R Pretorius, Mohammed A Aldahmesh, Fowzan S Alkuraya, et al.
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