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Molecular Biology Reports|May 5, 2021
Possible ethnic associations in primary hyperoxaluria type-III-associated HOGA1 sequence variantsAiysha AbidHuman Mutation|October 19, 2022
HOGA1 gene pathogenic variants in primary hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic associationAiysha Abid, Ali Raza, Tahir Aziz, et al.JPMA. the Journal of the Pakistan Medical Association|December 1, 2011
Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotypeSayed Hajan Shah, Aiysha Abid, Saba Shahid, et al.Molecular Biology Reports|February 28, 2023
The prevalence of pharmacogenetic variants of vitamin K epoxide reductase complex subunit 1 gene (rs9923231), cytochrome P450 family 2 subfamily C member 9 gene (rs1799853) and cytochrome P450 family 3 subfamily-A member-5 gene (rs776746) among 13 ethnic groups of PakistanSadaf Firasat, Ali Raza, Abdul Rafay Khan, et al.Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|April 2, 2011
Genetic heterogeneity for autosomal dominant familial hypertrophic cardiomyopathy in a Pakistani familyAiysha Abid, Naveed Akhtar, Shagufta Khaliq, et al.The Pharmacogenomics Journal|January 7, 2020
CYP3A5 gene polymorphisms and their impact on dosage and trough concentration of tacrolimus among kidney transplant patients: a systematic review and meta-analysisAbdul Rafay Khan, Ali Raza, Sadaf Firasat, et al.Journal of Human Genetics|August 10, 2006
Refinement of the locus for autosomal recessive cone-rod dystrophy (CORD8) linked to chromosome 1q23-q24 in a Pakistani family and exclusion of candidate genesMuhammad Ismail, Aiysha Abid, Khalid Anwar, et al.Frontiers in Genetics|July 18, 2018
Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic SyndromeAiysha Abid, Saba Shahid, Madiha Shakoor, et al.Evolutionary Bioinformatics Online|May 2, 2022
The Prevalence of Pharmacogenomics Variants and Their Clinical Relevance Among the Pakistani PopulationAbdul Rafay Khan, Sayed Hajan Shah, Sadia Ajaz, et al.Frontiers in Genetics|May 10, 2019
A Novel Nonsense Mutation in FERMT3 Causes LAD-III in a Pakistani FamilySaba Shahid, Samreen Zaidi, Shariq Ahmed, et al.Pageof 4