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Hemoglobin

Showing results (71-80 of 3,216) with videos related to

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Hemoglobin|July 17, 2015
First Detection of a Splice Acceptor Site β-Thalassemia Mutation: IVS-I-130 (HBB: c.93-1G > C) in a Chinese PatientSheng He, Qiang Zhang, Chenguang Zheng, et al.
Hemoglobin|June 4, 2015
The Incidence Rate of Acute Transfusion Reactions in Thalassemia Patients Referred to the Shiraz Thalassemia Centre, Shiraz, Iran, Before and After the Establishment of the Hemovigilance SystemLeila Kasraian, Mohammad H Karimi
Hemoglobin|July 22, 2015
Experimental Characterization of Hb Flurlingen (HBA2: c.177 C > G, p.His > Gln) and Hb Boghé (HBA2: c.177 C > A, p.His > Gln) Reveals Contradictory HBA2 Expression and Translation Patterns Despite Identical Amino Acid SubstitutionsTalal Qadah, Jill Finlayson, Maxine Dennis, et al.
Hemoglobin|January 1, 1989
Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb SJ F Codrington, F A Codrington, J H Wisse, et al.
Hemoglobin|June 20, 2015
Thalassemia Phenotypes and Genotypes in Taiwan: A Retrospective Study Based on Thalassemia Screening of Young Men for Military ConscriptionHsiao-Wei Lee, Shao-Min Han, Youngsen Yang, et al.
Hemoglobin|October 23, 2019
Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α<sup>0</sup>-Thalassemia (- -<sup>SEA</sup> deletion) Allele and Application for Double-Check Diagnosis of Hb Bart's Hydrops Fetalis Syndrome in ThailandWittaya Jomoui, Wanicha Tepakhan, Rossarin Karnpean
Hemoglobin|January 10, 2018
Hb Mozhaisk [β92(F8)His→Arg; HBB: c.278A>G] as a De Novo Mutation in a Child of Mixed Ethnic OriginsElena Benzoni, Valentina Giannone, Laura Michetti, et al.
Hemoglobin|March 2, 2018
Analysis of Common β-Thalassemia Mutations in North VietnamLan Thi Thuong Vo, Trang Thu Nguyen, Hai Xuan Le, et al.
Hemoglobin|March 2, 2018
Characterization of Hb Bart's Hydrops Fetalis Caused by - -<sup>SEA</sup> and a Large Novel α<sup>0</sup>-Thalassemia DeletionSheng He, Jihui Li, Peng Huang, et al.
Hemoglobin|January 1, 1986
Hemoglobin J Iran alpha 2 beta 2 77 (EF1) his----Asp in a Russian-Armenian familyJ Delanoe-Garin, M D Rhoda, C T Craescu, et al.
Pageof 322

Showing results (71-80 of 3,216) with videos related to

Sort By:
Pageof 322
Hemoglobin|July 17, 2015
First Detection of a Splice Acceptor Site β-Thalassemia Mutation: IVS-I-130 (HBB: c.93-1G > C) in a Chinese PatientSheng He, Qiang Zhang, Chenguang Zheng, et al.
Hemoglobin|June 4, 2015
The Incidence Rate of Acute Transfusion Reactions in Thalassemia Patients Referred to the Shiraz Thalassemia Centre, Shiraz, Iran, Before and After the Establishment of the Hemovigilance SystemLeila Kasraian, Mohammad H Karimi
Hemoglobin|July 22, 2015
Experimental Characterization of Hb Flurlingen (HBA2: c.177 C > G, p.His > Gln) and Hb Boghé (HBA2: c.177 C > A, p.His > Gln) Reveals Contradictory HBA2 Expression and Translation Patterns Despite Identical Amino Acid SubstitutionsTalal Qadah, Jill Finlayson, Maxine Dennis, et al.
Hemoglobin|January 1, 1989
Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb SJ F Codrington, F A Codrington, J H Wisse, et al.
Hemoglobin|June 20, 2015
Thalassemia Phenotypes and Genotypes in Taiwan: A Retrospective Study Based on Thalassemia Screening of Young Men for Military ConscriptionHsiao-Wei Lee, Shao-Min Han, Youngsen Yang, et al.
Hemoglobin|October 23, 2019
Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α<sup>0</sup>-Thalassemia (- -<sup>SEA</sup> deletion) Allele and Application for Double-Check Diagnosis of Hb Bart's Hydrops Fetalis Syndrome in ThailandWittaya Jomoui, Wanicha Tepakhan, Rossarin Karnpean
Hemoglobin|January 10, 2018
Hb Mozhaisk [β92(F8)His→Arg; HBB: c.278A>G] as a De Novo Mutation in a Child of Mixed Ethnic OriginsElena Benzoni, Valentina Giannone, Laura Michetti, et al.
Hemoglobin|March 2, 2018
Analysis of Common β-Thalassemia Mutations in North VietnamLan Thi Thuong Vo, Trang Thu Nguyen, Hai Xuan Le, et al.
Hemoglobin|March 2, 2018
Characterization of Hb Bart's Hydrops Fetalis Caused by - -<sup>SEA</sup> and a Large Novel α<sup>0</sup>-Thalassemia DeletionSheng He, Jihui Li, Peng Huang, et al.
Hemoglobin|January 1, 1986
Hemoglobin J Iran alpha 2 beta 2 77 (EF1) his----Asp in a Russian-Armenian familyJ Delanoe-Garin, M D Rhoda, C T Craescu, et al.
Pageof 322