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American Journal of Translational Research
|
November 11, 2016
Mutation near the binding interfaces at α-hemoglobin stabilizing protein is highly pathogenic
Jesu Francis Borgio, Mohammed S Al-Madan, Sayed AbdulAzeez
Archives of Medical Science : AMS
|
January 31, 2018
<i>KLF1</i> gene and borderline hemoglobin A<sub>2</sub> in Saudi population
J Francis Borgio, Sayed AbdulAzeez, Ahmed M Al-Muslami, et al.
Blood Cells, Molecules & Diseases
|
July 29, 2014
A novel HBA2 gene conversion in cis or trans: "α12 allele" in a Saudi population
J Francis Borgio, S AbdulAzeez, Awatif N Al-Nafie, et al.
Scientific Reports
|
December 10, 2023
Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts
Amein K Al-Ali, Abdullah M Al-Rubaish, Rudaynah A Alali, et al.
Blood Cells, Molecules & Diseases
|
May 16, 2015
Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients
Awatif N Al-Nafie, J Francis Borgio, Sayed AbdulAzeez, et al.
International Journal of Molecular Sciences
|
March 22, 2016
Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population
Sayed AbdulAzeez, Awatif N Al-Nafie, Abdullah Al-Shehri, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
American Journal of Translational Research
|
November 11, 2016
Mutation near the binding interfaces at α-hemoglobin stabilizing protein is highly pathogenic
Jesu Francis Borgio, Mohammed S Al-Madan, Sayed AbdulAzeez
Archives of Medical Science : AMS
|
January 31, 2018
<i>KLF1</i> gene and borderline hemoglobin A<sub>2</sub> in Saudi population
J Francis Borgio, Sayed AbdulAzeez, Ahmed M Al-Muslami, et al.
Blood Cells, Molecules & Diseases
|
July 29, 2014
A novel HBA2 gene conversion in cis or trans: "α12 allele" in a Saudi population
J Francis Borgio, S AbdulAzeez, Awatif N Al-Nafie, et al.
Scientific Reports
|
December 10, 2023
Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts
Amein K Al-Ali, Abdullah M Al-Rubaish, Rudaynah A Alali, et al.
Blood Cells, Molecules & Diseases
|
May 16, 2015
Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients
Awatif N Al-Nafie, J Francis Borgio, Sayed AbdulAzeez, et al.
International Journal of Molecular Sciences
|
March 22, 2016
Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population
Sayed AbdulAzeez, Awatif N Al-Nafie, Abdullah Al-Shehri, et al.
Page
of 1