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Urolithiasis|June 9, 2022
Primary hyperoxaluria and genetic linkages: an insight into the disease burden from PakistanSeema Hashmi, Aiysha Abid, Sajid Sultan, et al.
Immunological Investigations|July 13, 2013
HLA class I and II polymorphisms in the Gujjar population from PakistanAli Raza, Sadaf Firasat, Shagufta Khaliq, et al.
BMC Medical Genetics|August 27, 2020
Osteopontin promoter polymorphisms and risk of urolithiasis: a candidate gene association and meta-analysis studyAli Amar, Ayesha Afzal, Athar Hameed, et al.
Frontiers in Genetics|July 14, 2020
Novel Genetic Variations in Acute Myeloid Leukemia in Pakistani PopulationSaba Shahid, Muhammad Shakeel, Saima Siddiqui, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|May 2, 2023
Rare and heterogeneous manifestations of leucocyte adhesion deficiency type 1: report of two cases with diagnostic dilemmas and novel ITGB2 mutationSabiha Anis, Aiysha Abid, Sadaf Aba Umer Kodwavwala, et al.
Experimental Eye Research|February 8, 2003
Mutation screening of Pakistani families with congenital eye disordersShagufta Khaliq, Aiysha Abid, Abdul Hameed, et al.
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