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Showing results (1091-1100 of 2,379) with videos related to
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Hemoglobin
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July 3, 2014
Prevalence of depression in patients with β-thalassemia as assessed by the Beck's Depression Inventory
Akbar Shafiee, Shiva Nazari, Soudeh Jorjani, et al.
Hemoglobin
|
January 1, 1990
A new alpha chain variant Hb Tonosho [alpha 110(G17)Ala----Thr]: subunit dissociation during cation exchange chromatography for Hb A1c assay
Y Ohba, K Fujisawa, K Imai, et al.
Hemoglobin
|
January 1, 1990
A new beta-thalassemia mutation produced by a single nucleotide substitution in the conserved dinucleotide sequence of the IVS-I consensus acceptor site (AG----AA)
G Deidda, A Novelletto, M Hafez, et al.
Hemoglobin
|
February 11, 2015
Coinheritance of Hb D-Punjab and β-thalassemia: diagnosis and implications in prenatal diagnosis
Sheila Das, Ranjeet S Mashon
Hemoglobin
|
April 26, 2021
Serum Zinc Level in β-Thalassemia Major: A Retrospective Study in Southwest Iran
Somayeh Z Zardkhoni, Abdolkarim G Moghaddam, Fariba Rad, et al.
Hemoglobin
|
July 1, 1997
Hb Seal Rock [(alpha 2)142 term-->Glu, codon 142 TAA-->GAA]: an extended alpha chain variant associated with anemia, microcytosis, and alpha-thalassemia-2 (-3.7 Kb)
D Merritt, R T Jones, C Head, et al.
Hemoglobin
|
August 6, 2016
Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family
Sheng He, Li Lin, Yuan Wei, et al.
Hemoglobin
|
August 6, 2016
The -(α)(5.2) Deletion Detected in a Uruguayan Family: First Case Report in the Americas
Ana María Soler, Magdalena Schelotto, Natalia de Oliveira Mota, et al.
Hemoglobin
|
July 17, 2015
Aging in Sickle Cell Disease: Co-morbidities and New Issues in Management
Manpreet K Sandhu, Alice Cohen
Hemoglobin
|
April 18, 2015
Detection of Hb Constant Spring (HBA2: c.427T>C) Heterozygotes in Combination with β-Thalassemia or Hb E Trait by Capillary Electrophoresis
Sakorn Pornprasert, Supansa Saoboontan, Manoo Punyamung
Page
of 238
Search research articles
Search
Showing results (1091-1100 of 2,379) with videos related to
Sort By:
Page
of 238
Hemoglobin
|
July 3, 2014
Prevalence of depression in patients with β-thalassemia as assessed by the Beck's Depression Inventory
Akbar Shafiee, Shiva Nazari, Soudeh Jorjani, et al.
Hemoglobin
|
January 1, 1990
A new alpha chain variant Hb Tonosho [alpha 110(G17)Ala----Thr]: subunit dissociation during cation exchange chromatography for Hb A1c assay
Y Ohba, K Fujisawa, K Imai, et al.
Hemoglobin
|
January 1, 1990
A new beta-thalassemia mutation produced by a single nucleotide substitution in the conserved dinucleotide sequence of the IVS-I consensus acceptor site (AG----AA)
G Deidda, A Novelletto, M Hafez, et al.
Hemoglobin
|
February 11, 2015
Coinheritance of Hb D-Punjab and β-thalassemia: diagnosis and implications in prenatal diagnosis
Sheila Das, Ranjeet S Mashon
Hemoglobin
|
April 26, 2021
Serum Zinc Level in β-Thalassemia Major: A Retrospective Study in Southwest Iran
Somayeh Z Zardkhoni, Abdolkarim G Moghaddam, Fariba Rad, et al.
Hemoglobin
|
July 1, 1997
Hb Seal Rock [(alpha 2)142 term-->Glu, codon 142 TAA-->GAA]: an extended alpha chain variant associated with anemia, microcytosis, and alpha-thalassemia-2 (-3.7 Kb)
D Merritt, R T Jones, C Head, et al.
Hemoglobin
|
August 6, 2016
Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family
Sheng He, Li Lin, Yuan Wei, et al.
Hemoglobin
|
August 6, 2016
The -(α)(5.2) Deletion Detected in a Uruguayan Family: First Case Report in the Americas
Ana María Soler, Magdalena Schelotto, Natalia de Oliveira Mota, et al.
Hemoglobin
|
July 17, 2015
Aging in Sickle Cell Disease: Co-morbidities and New Issues in Management
Manpreet K Sandhu, Alice Cohen
Hemoglobin
|
April 18, 2015
Detection of Hb Constant Spring (HBA2: c.427T>C) Heterozygotes in Combination with β-Thalassemia or Hb E Trait by Capillary Electrophoresis
Sakorn Pornprasert, Supansa Saoboontan, Manoo Punyamung
Page
of 238