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Genetic Testing and Molecular Biomarkers|September 13, 2016
Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle GlaucomaAltaf A Kondkar, Ahmed Mousa, Taif A Azad, et al.Ophthalmic Genetics|August 20, 2013
Partial duplication of chromosome 19 associated with syndromic duane retraction syndromeKhaled K Abu-Amero, Altaf A Kondkar, Abdullah Al Otaibi, et al.Journal of Negative Results in Biomedicine|February 4, 2017
Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patientsAltaf A Kondkar, Nikhil B Edward, Hatem Kalantan, et al.Biology|January 26, 2024
Common Variants rs429358 and rs7412 in APOE Gene Are Not Associated with POAG in a Saudi CohortAltaf A Kondkar, Tahira Sultan, Taif A Azad, et al.Genes|December 23, 2023
Association between Polymorphism rs61876744 in PNPLA2 Gene and Keratoconus in a Saudi CohortAltaf A Kondkar, Taif A Azad, Tahira Sultan, et al.International Journal of Molecular Sciences|April 27, 2024
The Logistical Backbone of Photoreceptor Cell Function: Complementary Mechanisms of Dietary Vitamin A Receptors and Rhodopsin TransportersMatthias Leung, Jeremy Steinman, Dorothy Li, et al.Journal of Negative Results in Biomedicine|June 27, 2017
Polymorphism rs547984 on human chromosome 1q43 is not associated with primary open angle glaucoma in a Saudi cohortTaif A Azad, Nikhil B Edward, Altaf A Kondkar, et al.Ophthalmic Genetics|February 15, 2013
Ophthalmologic observations in a patient with partial mosaic trisomy 8Khaled K Abu-Amero, Altaf A Kondkar, Mustafa A Salih, et al.International Journal of Molecular Sciences|April 27, 2024
APOE ε2-Carriers Are Associated with an Increased Risk of Primary Angle-Closure Glaucoma in Patients of Saudi OriginAltaf A Kondkar, Taif A Azad, Tahira Sultan, et al.Cells|June 2, 2021
Loss of Motor Protein MYO1C Causes Rhodopsin Mislocalization and Results in Impaired Visual FunctionAshish K Solanki, Manas R Biswal, Stephen Walterhouse, et al.Pageof 9