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Showing results (991-1000 of 2,379) with videos related to
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Hemoglobin
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October 15, 2020
Heterozygosity for the Novel <i>HBA2</i>: c.*91_*92delTA Polyadenylation Site Variant on the α2-Globin Gene Expanding the Genetic Spectrum of α-Thalassemia in Iran
Fatemeh Forouzesh Pour, Keyvan Karimi, Zhila Ghaderi, et al.
Hemoglobin
|
October 7, 2020
Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A<sub>2</sub> Levels
Surada Satthakarn, Sitthichai Panyasai, Sakorn Pornprasert
Hemoglobin
|
November 30, 2018
Relationship Between Social Determinants of Health and the Thalassemia Prenatal Diagnosis Test in Zahedan, South Eastern Iran
Narjes Sargolzaie, Mostafa Montazer Zohour, Erfan Ayubi, et al.
Hemoglobin
|
February 13, 2019
<i>Krüppel-Like Factor 1</i> Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia
Ahmad Tamaddoni, Sahar Khabaz Astaneh, Reza Tabaripour, et al.
Hemoglobin
|
November 23, 2020
High Prevalence of Anemia and Inherited Hemoglobin Disorders in Tribal Populations of Madhya Pradesh State, India
Sonam Chourasia, Ravindra Kumar, Mendi P S S Singh, et al.
Hemoglobin
|
February 22, 2018
Molecular Characteristics of Hb New York [β113(G15)Val→Glu, HBB: c.341T>A] in Thailand
Attawut Chaibunruang, Kritsada Singha, Hataichanok Srivorakun, et al.
Hemoglobin
|
January 28, 2020
Hb F-Wentzville [<sup>G</sup>γ24(B6)Gly→Glu; <i>HBG2</i>: c.74G>A, p.Gly25Glu]: An Unstable <sup>G</sup>γ-Globin Variant Associated with Neonatal Hemolytic Anemia
Katarina M Semkiu, Jennifer L Oliveira, Phuong L Nguyen, et al.
Hemoglobin
|
September 20, 2014
The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia
Pimlak Charoenkwan, Pimjan Teerachaimahit, Torpong Sanguansermsri
Hemoglobin
|
April 28, 2016
The Impact of XmnI-HBG2, BCL11A and HBS1L-MYB Single Nucleotide Polymorphisms on Hb F Variation of Hematologically Normal Iranian Individuals
Elaheh Keyhani, Mahjoobeh Jafari Vesiehsari, Setareh Talebi Kakroodi, et al.
Hemoglobin
|
November 9, 2020
Association of Exon 14 of the <i>SOX6</i> Gene Sequence Variations with Response to Hydroxyurea Therapy in Patients Carrying Non Transfusion-Dependent Thalassemia
Zahra Mohammadi, Reza Mohammadi, Sezaneh Haghpanah, et al.
Page
of 238
Search research articles
Search
Showing results (991-1000 of 2,379) with videos related to
Sort By:
Page
of 238
Hemoglobin
|
October 15, 2020
Heterozygosity for the Novel <i>HBA2</i>: c.*91_*92delTA Polyadenylation Site Variant on the α2-Globin Gene Expanding the Genetic Spectrum of α-Thalassemia in Iran
Fatemeh Forouzesh Pour, Keyvan Karimi, Zhila Ghaderi, et al.
Hemoglobin
|
October 7, 2020
Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A<sub>2</sub> Levels
Surada Satthakarn, Sitthichai Panyasai, Sakorn Pornprasert
Hemoglobin
|
November 30, 2018
Relationship Between Social Determinants of Health and the Thalassemia Prenatal Diagnosis Test in Zahedan, South Eastern Iran
Narjes Sargolzaie, Mostafa Montazer Zohour, Erfan Ayubi, et al.
Hemoglobin
|
February 13, 2019
<i>Krüppel-Like Factor 1</i> Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia
Ahmad Tamaddoni, Sahar Khabaz Astaneh, Reza Tabaripour, et al.
Hemoglobin
|
November 23, 2020
High Prevalence of Anemia and Inherited Hemoglobin Disorders in Tribal Populations of Madhya Pradesh State, India
Sonam Chourasia, Ravindra Kumar, Mendi P S S Singh, et al.
Hemoglobin
|
February 22, 2018
Molecular Characteristics of Hb New York [β113(G15)Val→Glu, HBB: c.341T>A] in Thailand
Attawut Chaibunruang, Kritsada Singha, Hataichanok Srivorakun, et al.
Hemoglobin
|
January 28, 2020
Hb F-Wentzville [<sup>G</sup>γ24(B6)Gly→Glu; <i>HBG2</i>: c.74G>A, p.Gly25Glu]: An Unstable <sup>G</sup>γ-Globin Variant Associated with Neonatal Hemolytic Anemia
Katarina M Semkiu, Jennifer L Oliveira, Phuong L Nguyen, et al.
Hemoglobin
|
September 20, 2014
The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia
Pimlak Charoenkwan, Pimjan Teerachaimahit, Torpong Sanguansermsri
Hemoglobin
|
April 28, 2016
The Impact of XmnI-HBG2, BCL11A and HBS1L-MYB Single Nucleotide Polymorphisms on Hb F Variation of Hematologically Normal Iranian Individuals
Elaheh Keyhani, Mahjoobeh Jafari Vesiehsari, Setareh Talebi Kakroodi, et al.
Hemoglobin
|
November 9, 2020
Association of Exon 14 of the <i>SOX6</i> Gene Sequence Variations with Response to Hydroxyurea Therapy in Patients Carrying Non Transfusion-Dependent Thalassemia
Zahra Mohammadi, Reza Mohammadi, Sezaneh Haghpanah, et al.
Page
of 238