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Acta Biochimica Polonica|November 24, 2016
Compound heterozygous LDLR variant in severely affected familial hypercholesterolemia patientFaisal A Al-Allaf, Abdullah Alashwal, Zainularifeen Abduljaleel, et al.
Atherosclerosis|October 2, 2018
Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemiaFahad Alnouri, Mohammad Athar, Faisal A Al-Allaf, et al.
Journal of Clinical Medicine Research|March 9, 2017
Molecular Analysis of Factor VIII and Factor IX Genes in Hemophilia Patients: Identification of Novel Mutations and Molecular Dynamics StudiesFaisal A Al-Allaf, Mohiuddin M Taher, Zainularifeen Abduljaleel, et al.
Molecular Genetics and Genomics : MGG|February 25, 2014
DNA mismatch repair MSH2 gene-based SNP associated with different populationsZainularifeen Abduljaleel, Faisal A Al-Allaf, Wajahatullah Khan, et al.
International Medical Case Reports Journal|May 6, 2020
Adamantinomatous Craniopharyngioma in an Adult: A Case Report with NGS AnalysisRaid A Jastania, Muhammad Saeed, Hisham Al-Khalidi, et al.
Diabetes Research and Clinical Practice|July 28, 2015
A novel SNP in 3' UTR of INS gene: A case report of neonatal diabetes mellitusNeda M Bogari, Husni H Rayes, Fakri Mostafa, et al.
Plos One|March 26, 2014
Evidence of trem2 variant associated with triple risk of Alzheimer's diseaseZainularifeen Abduljaleel, Faisal A Al-Allaf, Wajahatullah Khan, et al.
Disease Markers|February 25, 2021
Next Generation Exome Sequencing of Pediatric Asthma Identifies Rare and Novel Variants in Candidate GenesNeda M Bogari, Amr A Amin, Husni H Rayes, et al.
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