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Molecular Vision|December 2, 2005
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 geneQingjiong Zhang, Fareeha Zulfiqar, S Amer Riazuddin, et al.
Acta Tropica|December 20, 2024
ToRCH pathogens-induced histopathological changes in placental tissues and associated post obstetric complicationsMaryam Naseem, Sanaullah Khan, Dalal Sulaiman Alshaya, et al.
Cureus|November 29, 2024
Efficacy of Different Beta Blockers in Reducing Mortality in Heart-Failure PatientsSalman Habib Roghani, Dr Sanaullah Khan, Aatika Shafiq, et al.
The Journal of Clinical Investigation|February 7, 2018
Modifier variant of METTL13 suppresses human GAB1-associated profound deafnessRizwan Yousaf, Zubair M Ahmed, Arnaud Pj Giese, et al.
International Journal of Biological Macromolecules|January 14, 2018
Interaction between structurally different heteroexopolysaccharides and β-lactoglobulin studied by solution scattering and analytical ultracentrifugationSanaullah Khan, Johnny Birch, Marie-Rose Van Calsteren, et al.
Molecular Vision|July 24, 2013
Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophyFiroz Kabir, Shagufta Naz, S Amer Riazuddin, et al.
Investigative Ophthalmology & Visual Science|June 28, 2005
Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani familiesS Amer Riazuddin, Fareeha Zulfiqar, Qingjiong Zhang, et al.
Genetic Vaccines and Therapy|January 8, 2011
Hepatitis C virus genotype 3a with phylogenetically distinct origin is circulating in PakistanIrshad-Ur Rehman, Muhammad Idrees, Muhammad Ali, et al.
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