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Molecular Vision|August 21, 2009
High-resolution analysis of DNA copy number alterations in patients with primary open-angle glaucomaKhaled K Abu-Amero, Ali Hellani, Patrick Bender, et al.
Ophthalmic Genetics|February 6, 2016
Duane retraction syndrome in a patient with Duchenne muscular dystrophyThomas M Bosley, Mustafa A Salih, Hisham Alkhalidi, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 1, 2014
HOXA1 Mutations are Not Commonly Associated with Non-Syndromic DeafnessKhaled K Abu-Amero, Abdulrahman al Hagr, Murad O Almomani, et al.
Molecular Vision|May 10, 2011
Down-regulation of OPA1 in patients with primary open angle glaucomaThomas M Bosley, Ali Hellani, George L Spaeth, et al.
Ophthalmic Genetics|September 7, 2012
Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorderKhaled K Abu-Amero, Altaf A Kondkar, Mustafa A M Salih, et al.
Ophthalmic Genetics|April 23, 2011
Horizontal gaze palsy and progressive scoliosis without ROBO3 mutationsKhaled K Abu-Amero, Flavio Faletra, Paolo Gasparini, et al.
Ophthalmic Genetics|February 5, 2013
Xq26.3 microdeletion in a male with Wildervanck SyndromeKhaled K Abu-Amero, Altaf A Kondkar, Ibrahim A Alorainy, et al.
Ophthalmic Genetics|February 10, 2010
Ophthalmologic abnormalities in a de novo terminal 6q deletionKhaled K Abu-Amero, Ali Hellani, Mustafa A Salih, et al.
Ophthalmic Genetics|June 23, 2010
Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomyKhaled K Abu-Amero, Ali Hellani, Mustafa A Salih, et al.
Investigative Ophthalmology & Visual Science|July 7, 2009
Synergistic divergence: a distinct ocular motility dysinnervation patternDarren T Oystreck, Arif O Khan, Antonio Aguirre Vila-Coro, et al.
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