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	1.	Corneal ectasia and hydrops in a patient with autosomal recessive cornea plana. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed Meyer, Brian Producer: 20061026 In: Ophthalmic genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Recessive cornea plana in the Kingdom of Saudi Arabia. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed Meyer, Brian Producer: 20061013 In: Ophthalmology vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The enhanced S-cone syndrome in children. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed Meyer, Brian Producer: 20070327 In: The British journal of ophthalmology vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Correlation of ophthalmic examination with carrier status in females potentially harboring a severe Norrie disease gene mutation. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Meyer, Brian Producer: 20080501 In: Ophthalmology vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Congenital hereditary endothelial dystrophy, not glaucoma, in a child with iris colobomas. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Alkuraya, Fowzan Producer: 20180417 In: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis). [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Alkuraya, Fowzan S Producer: 20160706 In: Transactions of the American Ophthalmological Society vol. 113 Availability: No items available. Save to lists Add to cart (remove)
	7.	Clinical Characterization of LRPAP1-Related Pediatric High Myopia. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Alkuraya, Fowzan S Producer: 20160607 In: Ophthalmology vol. 123 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma - a distinct phenotype caused by recessive LTBP2 mutations. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Alkuraya, Fowzan S Producer: 20120210 In: Molecular vision vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	9.	Brittle cornea without clinically-evident extraocular findings in an adult harboring a novel homozygous ZNF469 mutation. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Alkuraya, Fowzan S Producer: 20130326 In: Ophthalmic genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Genetic and genomic analysis of classic aniridia in Saudi Arabia. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Alkuraya, Fowzan S Producer: 20110616 In: Molecular vision vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	11.	Infantile Nephropathic Cystinosis: A Novel [electronic resource] by Doneray, Hakan Aldahmesh, Mohammed Yilmaz, Gulsah Cinici, Emine Orbak, Zerrin Publication details: The Eurasian journal of medicine Jun 2017 In: The Eurasian journal of medicine vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Novel recessive BFSP2 and PITX3 mutations: insights into mutational mechanisms from consanguineous populations. [electronic resource] by Aldahmesh, Mohammed A Khan, Arif O Mohamed, Jawahir Alkuraya, Fowzan S Producer: 20120328 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Recessive mutations in LEPREL1 underlie a recognizable lens subluxation phenotype. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Alsharif, Hadeel Alkuraya, Fowzan S Producer: 20150805 In: Ophthalmic genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Childhood cone-rod dystrophy with macular cystic degeneration from recessive CRB1 mutation. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Abu-Safieh, Leen Alkuraya, Fowzan S Producer: 20150811 In: Ophthalmic genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Congenital glaucoma with acquired peripheral circumferential iris degeneration. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Mohamed, Jawahir Y Alkuraya, Fowzan S Producer: 20130614 In: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Juvenile cataract morphology in 3 siblings not yet diagnosed with cerebrotendinous xanthomatosis. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Mohamed, Jawaher Y Alkuraya, Fowzan S Producer: 20130625 In: Ophthalmology vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Familial blepharophimosis-like syndrome with esotropia, uveal coloboma, and short stature. [electronic resource] by Khan, Arif O Alam, Syed K Aldahmesh, Mohammed Rajab, Mohammed Meyer, Brian Producer: 20061026 In: Ophthalmic genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Mutational spectrum of SLC4A11 in autosomal recessive CHED in Saudi Arabia. [electronic resource] by Aldahmesh, Mohammed A Khan, Arif O Meyer, Brian F Alkuraya, Fowzan S Producer: 20090918 In: Investigative ophthalmology & visual science vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Helicoid subretinal fibrosis associated with a novel recessive NR2E3 mutation p.S44X. [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Al-Harthi, Essam Alkuraya, Fowzan S Producer: 20100401 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 128 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Phenotype-genotype correlation in potential female carriers of X-linked developmental cataract (Nance-Horan syndrome). [electronic resource] by Khan, Arif O Aldahmesh, Mohammed A Mohamed, Jawahir Y Alkuraya, Fowzan S Producer: 20120926 In: Ophthalmic genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 63 results.