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Bader Almuzzaini

Showing results (21-30 of 29) with videos related to

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Cancer Medicine|November 3, 2021
Discovery of a novel potentially transforming somatic mutation in CSF2RB gene in breast cancerMamoon Rashid, Rizwan Ali, Bader Almuzzaini, et al.
The Pharmacogenomics Journal|February 5, 2023
Targeted next-generation sequencing of genes involved in Warfarin Pharmacodynamics and pharmacokinetics pathways using the Saudi Warfarin Pharmacogenetic study (SWAP)Maha Al Ammari, Bader Almuzzaini, Khalid Al Sulaiman, et al.
Frontiers in Genetics|August 29, 2022
Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genesManal Alaamery, Jahad Alghamdi, Salam Massadeh, et al.
AIMS Public Health|September 24, 2020
Epidemiology of cancer in Saudi Arabia thru 2010-2019: a systematic review with constrained meta-analysisWedad Saeed Alqahtani, Nawaf Abdulrahman Almufareh, Dalia Mostafa Domiaty, et al.
Journal of Personalized Medicine|July 2, 2021
Identification of Novel Mutations in Colorectal Cancer Patients Using AmpliSeq Comprehensive Cancer PanelBader Almuzzaini, Jahad Alghamdi, Alhanouf Alomani, et al.
European Journal of Medical Genetics|May 16, 2020
Biallelic variants in four genes underlying recessive osteogenesis imperfectaAmir Hayat, Shabir Hussain, Muhammad Bilal, et al.
Genomics|April 10, 2021
Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortalityJahad Alghamdi, Manal Alaamery, Tlili Barhoumi, et al.
Annals of Clinical and Translational Neurology|September 27, 2019
Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screeningMajid Alfadhel, Muhammad Umair, Bader Almuzzaini, et al.
Genes|March 6, 2021
Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo <i>CDC42</i> Gene Defect: Expanding the Molecular and Phenotypic SpectrumAbdulaziz Asiri, Deemah Alwadaani, Muhammad Umair, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Cancer Medicine|November 3, 2021
Discovery of a novel potentially transforming somatic mutation in CSF2RB gene in breast cancerMamoon Rashid, Rizwan Ali, Bader Almuzzaini, et al.
The Pharmacogenomics Journal|February 5, 2023
Targeted next-generation sequencing of genes involved in Warfarin Pharmacodynamics and pharmacokinetics pathways using the Saudi Warfarin Pharmacogenetic study (SWAP)Maha Al Ammari, Bader Almuzzaini, Khalid Al Sulaiman, et al.
Frontiers in Genetics|August 29, 2022
Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genesManal Alaamery, Jahad Alghamdi, Salam Massadeh, et al.
AIMS Public Health|September 24, 2020
Epidemiology of cancer in Saudi Arabia thru 2010-2019: a systematic review with constrained meta-analysisWedad Saeed Alqahtani, Nawaf Abdulrahman Almufareh, Dalia Mostafa Domiaty, et al.
Journal of Personalized Medicine|July 2, 2021
Identification of Novel Mutations in Colorectal Cancer Patients Using AmpliSeq Comprehensive Cancer PanelBader Almuzzaini, Jahad Alghamdi, Alhanouf Alomani, et al.
European Journal of Medical Genetics|May 16, 2020
Biallelic variants in four genes underlying recessive osteogenesis imperfectaAmir Hayat, Shabir Hussain, Muhammad Bilal, et al.
Genomics|April 10, 2021
Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortalityJahad Alghamdi, Manal Alaamery, Tlili Barhoumi, et al.
Annals of Clinical and Translational Neurology|September 27, 2019
Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screeningMajid Alfadhel, Muhammad Umair, Bader Almuzzaini, et al.
Genes|March 6, 2021
Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo <i>CDC42</i> Gene Defect: Expanding the Molecular and Phenotypic SpectrumAbdulaziz Asiri, Deemah Alwadaani, Muhammad Umair, et al.
Pageof 3