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Showing results (1081-1090 of 2,379) with videos related to
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Hemoglobin
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January 1, 1981
Hemoglobin Miyashiro (beta 23[B5] val substituting for gly) an electrophoretically silent variant discovered by the isopropanol test
T Nakatsuji, S Miwa, Y Ohba, et al.
Hemoglobin
|
January 1, 1981
Rat hemoglobin heterogeneity: postnatal changes in proportions of multiple components and effects of erythropoietin on marrow cell cultures
M C Datta, J G Gilman
Hemoglobin
|
January 1, 1989
Evidence for the single origin of HB G-San Jose in Sicily
L Cremonesi, M Travi, S Li Volti, et al.
Hemoglobin
|
July 2, 2020
Umbilical Cord Blood Screening for the Detection of Common Deletional Mutations of α-Thalassemia in Bangladesh
Saeed Anwar, Jarin Taslem Mourosi, Md Kamrul Hasan, et al.
Hemoglobin
|
July 2, 2020
A Woman with Missing Hb A<sub>2</sub> Due to a Novel (εγ)δβ<sup>0</sup>-Thalassemia and a Novel δ-Globin Variant Hb A<sub>2</sub>-Gebenstorf (<i>HBD</i>: c.209G>A)
Elisabeth Saller, Jeroen Knijnenburg, Cornelis L Harteveld, et al.
Hemoglobin
|
July 2, 2020
Necrobiosis Lipoidica in a Patient with β-Thalassemia Major: A Case Report and Review of the Literature
Evangelia Vetsiou, Vasileios Mpouras, Christina Nikolaidou, et al.
Hemoglobin
|
June 27, 2020
Micromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailand
Roongnalin Bunthupanich, Rossarin Karnpean, Anuwat Pinyachat, et al.
Hemoglobin
|
July 30, 2020
Novel α<sup>0</sup>-Thalassemia Deletion Identified in an Indian Infant with Hb H Disease
Jordyn A Moore, Beverley M Pullon, Kylie M Drake, et al.
Hemoglobin
|
July 3, 2014
Red cell indices and formulas used in differentiation of β-thalassemia trait from iron deficiency in Thai school children
Sakorn Pornprasert, Auttapon Panya, Manoo Punyamung, et al.
Hemoglobin
|
July 3, 2014
β-Thalassemia major resulting from compound heterozygosity for HBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a novel β(0)-thalassemia frameshift mutation: HBB: c.209delG; p.Gly70Valfs*20
Michelle L Kluge, James D Hoyer, Kenneth C Swanson, et al.
Page
of 238
Search research articles
Search
Showing results (1081-1090 of 2,379) with videos related to
Sort By:
Page
of 238
Hemoglobin
|
January 1, 1981
Hemoglobin Miyashiro (beta 23[B5] val substituting for gly) an electrophoretically silent variant discovered by the isopropanol test
T Nakatsuji, S Miwa, Y Ohba, et al.
Hemoglobin
|
January 1, 1981
Rat hemoglobin heterogeneity: postnatal changes in proportions of multiple components and effects of erythropoietin on marrow cell cultures
M C Datta, J G Gilman
Hemoglobin
|
January 1, 1989
Evidence for the single origin of HB G-San Jose in Sicily
L Cremonesi, M Travi, S Li Volti, et al.
Hemoglobin
|
July 2, 2020
Umbilical Cord Blood Screening for the Detection of Common Deletional Mutations of α-Thalassemia in Bangladesh
Saeed Anwar, Jarin Taslem Mourosi, Md Kamrul Hasan, et al.
Hemoglobin
|
July 2, 2020
A Woman with Missing Hb A<sub>2</sub> Due to a Novel (εγ)δβ<sup>0</sup>-Thalassemia and a Novel δ-Globin Variant Hb A<sub>2</sub>-Gebenstorf (<i>HBD</i>: c.209G>A)
Elisabeth Saller, Jeroen Knijnenburg, Cornelis L Harteveld, et al.
Hemoglobin
|
July 2, 2020
Necrobiosis Lipoidica in a Patient with β-Thalassemia Major: A Case Report and Review of the Literature
Evangelia Vetsiou, Vasileios Mpouras, Christina Nikolaidou, et al.
Hemoglobin
|
June 27, 2020
Micromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailand
Roongnalin Bunthupanich, Rossarin Karnpean, Anuwat Pinyachat, et al.
Hemoglobin
|
July 30, 2020
Novel α<sup>0</sup>-Thalassemia Deletion Identified in an Indian Infant with Hb H Disease
Jordyn A Moore, Beverley M Pullon, Kylie M Drake, et al.
Hemoglobin
|
July 3, 2014
Red cell indices and formulas used in differentiation of β-thalassemia trait from iron deficiency in Thai school children
Sakorn Pornprasert, Auttapon Panya, Manoo Punyamung, et al.
Hemoglobin
|
July 3, 2014
β-Thalassemia major resulting from compound heterozygosity for HBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a novel β(0)-thalassemia frameshift mutation: HBB: c.209delG; p.Gly70Valfs*20
Michelle L Kluge, James D Hoyer, Kenneth C Swanson, et al.
Page
of 238