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Genes|April 8, 2014
The molecular basis of retinal dystrophies in pakistanMuhammad Imran Khan, Maleeha Azam, Muhammad Ajmal, et al.
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.
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.
Molecular Biology Reports|February 8, 2012
Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patientsWaqas Ahmed, Muhammad Ajmal, Ahmed Sadeque, et al.
Investigative Ophthalmology & Visual Science|July 14, 2017
TNF-α Genetic Predisposition and Higher Expression of Inflammatory Pathway Components in KeratoconusMuneeza Arbab, Saira Tahir, Muhammad Khizar Niazi, et al.
Molecular Vision|April 6, 2013
Association of Pro12Ala polymorphism in peroxisome proliferator activated receptor gamma with proliferative diabetic retinopathyKhadija Tariq, Saira Bano Malik, Syeda Hafiza Benish Ali, et al.
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