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Hemoglobin

Showing results (591-600 of 3,217) with videos related to

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Hemoglobin|April 28, 2016
A Family with γ-Thalassemia and High Hb A2 LevelsGiulia Parmeggiani, Francesca Gualandi, Rita Selvatici, et al.
Hemoglobin|April 28, 2016
A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)]Jin-Mei Yan, Jian-Ying Zhou, Xing-Mei Xie, et al.
Hemoglobin|June 3, 2016
Population Screening for Hemoglobinopathy Profiling: Is the Development of a Microarray Worthwhile?Manousos E Kambouris
Hemoglobin|June 3, 2016
Hb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, IndiaSatyabrata Meher, Snehadhini Dehury, Pradeep Kumar Mohanty, et al.
Hemoglobin|November 11, 2017
Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive ProgramFan Jiang, Gui-Lan Chen, Jian Li, et al.
Hemoglobin|November 29, 2017
Characterization of Two Novel Deletions Involving the 5' Region of the β-Globin GeneJohn S Waye, Meredith Hanna, Betty-Ann Hohenadel, et al.
Hemoglobin|December 19, 2017
Coinheritance of α- and β-Thalassemia with a Novel Mutation (HBB: c.268_281delAGTGAGCTGCACTG) in a Chinese FamilyChuyun Cheng, Qi Peng, Siping Li, et al.
Hemoglobin|December 19, 2017
Enhancing Effect of Hydroxyurea on Hb F in Sickle Cell Disease: Ten-Year Egyptian ExperienceIlham Youssry, Amina Abdel-Salam, Rania Ismail, et al.
Hemoglobin|December 19, 2017
Hb A<sub>2</sub>-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A<sub>2</sub>-β-Thalassemia TraitGui-Lan Chen, Lv-Yin Huang, Jian-Ying Zhou, et al.
Hemoglobin|January 1, 1988
Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysisL Oggiano, F Dore, P Pistidda, et al.
Pageof 322

Showing results (591-600 of 3,217) with videos related to

Sort By:
Pageof 322
Hemoglobin|April 28, 2016
A Family with γ-Thalassemia and High Hb A2 LevelsGiulia Parmeggiani, Francesca Gualandi, Rita Selvatici, et al.
Hemoglobin|April 28, 2016
A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)]Jin-Mei Yan, Jian-Ying Zhou, Xing-Mei Xie, et al.
Hemoglobin|June 3, 2016
Population Screening for Hemoglobinopathy Profiling: Is the Development of a Microarray Worthwhile?Manousos E Kambouris
Hemoglobin|June 3, 2016
Hb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, IndiaSatyabrata Meher, Snehadhini Dehury, Pradeep Kumar Mohanty, et al.
Hemoglobin|November 11, 2017
Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive ProgramFan Jiang, Gui-Lan Chen, Jian Li, et al.
Hemoglobin|November 29, 2017
Characterization of Two Novel Deletions Involving the 5' Region of the β-Globin GeneJohn S Waye, Meredith Hanna, Betty-Ann Hohenadel, et al.
Hemoglobin|December 19, 2017
Coinheritance of α- and β-Thalassemia with a Novel Mutation (HBB: c.268_281delAGTGAGCTGCACTG) in a Chinese FamilyChuyun Cheng, Qi Peng, Siping Li, et al.
Hemoglobin|December 19, 2017
Enhancing Effect of Hydroxyurea on Hb F in Sickle Cell Disease: Ten-Year Egyptian ExperienceIlham Youssry, Amina Abdel-Salam, Rania Ismail, et al.
Hemoglobin|December 19, 2017
Hb A<sub>2</sub>-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A<sub>2</sub>-β-Thalassemia TraitGui-Lan Chen, Lv-Yin Huang, Jian-Ying Zhou, et al.
Hemoglobin|January 1, 1988
Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysisL Oggiano, F Dore, P Pistidda, et al.
Pageof 322