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Genetics and Molecular Biology|July 26, 2018
Decreased serum PON1 arylesterase activity in familial hypercholesterolemia patients with a mutated LDLR geneMuhammad Idrees, Abdul Rauf Siddiq, Muhammad Ajmal, et al.The Journal of General Virology|April 16, 2010
Patient HLA-DRB1* and -DQB1* allele and haplotype association with hepatitis C virus persistence and clearanceLubna Ali, Atika Mansoor, Nafees Ahmad, et al.Acta Diabetologica|September 2, 2019
Association of IGF1 and VEGFA polymorphisms with diabetic retinopathy in Pakistani populationNetasha Khan, Andrew D Paterson, Delnaz Roshandel, et al.Gene|July 28, 2024
Exploring WNT2 polymorphisms in comitant strabismus: A genetic association studyZainab Zehra, Christopher S von Bartheld, Andrea B Agarwal, et al.Neurogenetics|October 23, 2015
Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld-Rieger syndromeShazia Micheal, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, et al.European Journal of Gastroenterology & Hepatology|March 5, 2019
A 2-year retrospective study of viral and host-associated risk factors in Pakistani hepatocellular carcinoma patientsZain Ul Abideen, Shafiqa Siddique, Izza Nasrullah, et al.Genetic Testing and Molecular Biomarkers|April 5, 2011
A novel pathogenic nonsense triple-nucleotide mutation in the low-density lipoprotein receptor gene and its clinical correlation with familial hypercholesterolemiaMuhammad Ajmal, Waqas Ahmed, Naveed Akhtar, et al.Biochemical Genetics|August 20, 2021
Genetic Association of Butyrylcholinesterase with Major Depressive DisorderSliha Awan, Aisha N Hashmi, Rizwan Taj, et al.American Journal of Human Genetics|March 19, 2002
Y-chromosomal DNA variation in PakistanRaheel Qamar, Qasim Ayub, Aisha Mohyuddin, et al.Journal of Human Genetics|November 1, 2013
Novel mutation in AAA domain of BCS1L causing Bjornstad syndromeSaima Siddiqi, Saadat Siddiq, Atika Mansoor, et al.Pageof 11