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Ophthalmic Genetics|April 11, 2012
Familial spherophakia with short stature caused by a novel homozygous ADAMTS17 mutationArif O Khan, Mohammed A Aldahmesh, Huda Al-Ghadeer, 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.
Molecular Vision|July 28, 2009
Founder heterozygous P23T CRYGD mutation associated with cerulean (and coralliform) cataract in 2 Saudi familiesArif O Khan, Mohammed A Aldahmesh, Faisal E Ghadhfan, et al.
American Journal of Human Genetics|March 5, 2013
Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmiaFatema Zahrani, Mohammed A Aldahmesh, Muneera J Alshammari, et al.
American Journal of Ophthalmology|November 7, 2012
Biometric and molecular characterization of clinically diagnosed posterior microphthalmosSawsan R Nowilaty, Arif O Khan, Mohammed A Aldahmesh, et al.
Ophthalmic Genetics|November 28, 2009
Corneal decompensation in recessive cornea planaArif O Khan, Mohammed A Aldahmesh, Saeed Al-Gehedan, et al.
Human Mutation|July 3, 2013
The syndrome of microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) is caused by mutations in ADAMTS18Mohammed A Aldahmesh, Muneera J Alshammari, Arif O Khan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 1, 2012
Genomic analysis of pediatric cataract in Saudi Arabia reveals novel candidate disease genesMohammed A Aldahmesh, Arif O Khan, Jawahir Y Mohamed, et al.
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