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Journal of Affective Disorders|March 5, 2026
RELN biallelic variant as a candidate risk factor in a consanguineous Pakistani family with bipolar disorder and clinical heterogeneityAisha Nasir Hashmi, Ricardo S Haripaul, Tahir Muhammad, et al.
RSC Advances|April 15, 2022
Electrochemically driven optical and SERS immunosensor for the detection of a therapeutic cardiac drugMadeeha Chaudhry, Dong-Kwon Lim, Jeon Woong Kang, et al.
Plos One|December 30, 2015
Variants in the ASB10 Gene Are Associated with Primary Open Angle GlaucomaShazia Micheal, Humaira Ayub, Farrah Islam, et al.
Scientific Reports|February 19, 2016
Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7Kristof Van Schil, Marcus Karlstetter, Alexander Aslanidis, et al.
Clinical Genetics|April 13, 2026
Identification of 19 Pathogenic Variants in a Clinically Heterogeneous Cohort With Suspected Inborn Errors of MetabolismSumreena Mansoor, Sabeen Abid, Muhammad Imran, et al.
Clinical & Experimental Ophthalmology|August 6, 2014
Identification of novel CYP1B1 gene mutations in patients with primary congenital and primary open-angle glaucomaShazia Micheal, Humaira Ayub, Saemah N Zafar, et al.
Molecular Vision|January 14, 2010
Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohortsHumaira Ayub, Muhammad Imran Khan, Shazia Micheal, et al.
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