Showing results (41-50 of 104) with videos related to

Sort By:
Pageof 11
Cornea|April 1, 2016
Identification of Mutations in the PRDM5 Gene in Brittle Cornea SyndromeShazia Micheal, Muhammad Imran Khan, Farrah Islam, et al.
Investigative Ophthalmology & Visual Science|February 14, 2017
The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani FamiliesVafa Keser, Ayesha Khan, Sorath Siddiqui, et al.
Plos One|July 3, 2015
Clinical Utility of a Coronary Heart Disease Risk Prediction Gene Score in UK Healthy Middle Aged Men and in the Pakistani PopulationKatherine E Beaney, Jackie A Cooper, Saleem Ullah Shahid, et al.
The International Journal of Neuroscience|October 25, 2022
KIF1A novel frameshift variant p.(Ser887Profs*64) exhibits clinical heterogeneity in a Pakistani family with hereditary sensory and autonomic neuropathy type IICSaima Ghafoor, Muhammad Arshad Rafiq, Syed Tahir Abbas Shah, et al.
Current Pharmaceutical Biotechnology|February 4, 2021
Phytochemical Screening and Protective Effects of Prunus persica Seeds Extract on Carbon Tetrachloride-Induced Hepatic Injury in RatsSidra Rehman, Rubina Nazar, Azeem Mehmood Butt, et al.
The International Journal of Neuroscience|September 19, 2022
Association of dopamine β-hydroxylase polymorphism rs1611115 and serum levels with psychiatric disorders in Pakistani populationAisha Nasir Hashmi, Raees Ahmed Dharejo, Usama Bin Zubair, et al.
Molecular Vision|June 6, 2012
A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi diseaseNadia K Waheed, Ahmed H Qavi, Sarah N Malik, et al.
Molecular Biology Reports|November 18, 2010
Role of tissue plasminogen activator and plasminogen activator inhibitor polymorphism in myocardial infarctionWaqas Ahmed, Meera Malik, Imran Saeed, et al.
Genes|April 8, 2014
The molecular basis of retinal dystrophies in pakistanMuhammad Imran Khan, Maleeha Azam, Muhammad Ajmal, et al.
Molecular Vision|August 10, 2012
Identification of a novel FBN1 gene mutation in a large Pakistani family with Marfan syndromeShazia Micheal, Muhammad Imran Khan, Farah Akhtar, et al.
Pageof 11