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Hemoglobin

Showing results (161-170 of 3,216) with videos related to

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Hemoglobin|January 1, 1989
Hb Chandigarh or alpha 2 beta 2(94)(FG1)Asp----Gly observed in an Indian familyS Dash, J B Wilson, B B Webber, et al.
Hemoglobin|January 10, 2015
Hb Feilding [β12(A9)Thr → Pro; HBB: c.37A>C]: a novel unstable β-globin chain variantNikhil Ghallyan, Tarn Donald, David Broad, et al.
Hemoglobin|January 10, 2015
Rare hemoglobin variants: Hb G-Szuhu (HBB: c.243C>G), Hb G-Coushatta (HBB: c.68A>C) and Hb Mizuho (HBB: c.206T>C) in Sri Lankan familiesP Shiromi Perera, Ishari Silva, Menaka Hapugoda, et al.
Hemoglobin|November 6, 2014
Early onset of fetal hydrops associated with the α-thalassemia - -(THAI) deletionYu Yang, Dong-Zhi Li
Hemoglobin|November 6, 2014
Molecular characterization of a β-thalassemia intermedia patient presenting inferior vena cava thrombosis: interaction of the β-globin erythroid Krüppel-like factor binding site mutation with Hb E and α(+)-thalassemiaThanet Prajantasen, Nattiya Teawtrakul, Goonnapa Fucharoen, et al.
Hemoglobin|November 6, 2014
An Alu element-mediated 28.5 kb α-thalassemia deletion found in a Chinese familyJing Yu, Jun Xie, Liya Luo, et al.
Hemoglobin|September 15, 2015
Characterization of Clinical and Laboratory Profiles of the Deletional α2-Globin Gene Polyadenylation Signal Sequence (AATAAA > AATA- -) in an Indian PopulationPrashant Deshpande, Neelagandan Kamalanathan, Eswari Sampath, et al.
Hemoglobin|September 16, 2015
The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian AmazonAylla N L M Silva, Greice L Cardoso, Daniele A Cunha, et al.
Hemoglobin|October 20, 2015
Diagnosis of a Family with the Novel -α(21.9) Thalassemia DeletionJu Long, Wanrong Pang, Lei Sun, et al.
Hemoglobin|November 18, 2015
A Further Note on the Thalassemia Screening Program in the Muğla Region of TurkeyNejat Akar
Pageof 322

Showing results (161-170 of 3,216) with videos related to

Sort By:
Pageof 322
Hemoglobin|January 1, 1989
Hb Chandigarh or alpha 2 beta 2(94)(FG1)Asp----Gly observed in an Indian familyS Dash, J B Wilson, B B Webber, et al.
Hemoglobin|January 10, 2015
Hb Feilding [β12(A9)Thr → Pro; HBB: c.37A>C]: a novel unstable β-globin chain variantNikhil Ghallyan, Tarn Donald, David Broad, et al.
Hemoglobin|January 10, 2015
Rare hemoglobin variants: Hb G-Szuhu (HBB: c.243C>G), Hb G-Coushatta (HBB: c.68A>C) and Hb Mizuho (HBB: c.206T>C) in Sri Lankan familiesP Shiromi Perera, Ishari Silva, Menaka Hapugoda, et al.
Hemoglobin|November 6, 2014
Early onset of fetal hydrops associated with the α-thalassemia - -(THAI) deletionYu Yang, Dong-Zhi Li
Hemoglobin|November 6, 2014
Molecular characterization of a β-thalassemia intermedia patient presenting inferior vena cava thrombosis: interaction of the β-globin erythroid Krüppel-like factor binding site mutation with Hb E and α(+)-thalassemiaThanet Prajantasen, Nattiya Teawtrakul, Goonnapa Fucharoen, et al.
Hemoglobin|November 6, 2014
An Alu element-mediated 28.5 kb α-thalassemia deletion found in a Chinese familyJing Yu, Jun Xie, Liya Luo, et al.
Hemoglobin|September 15, 2015
Characterization of Clinical and Laboratory Profiles of the Deletional α2-Globin Gene Polyadenylation Signal Sequence (AATAAA > AATA- -) in an Indian PopulationPrashant Deshpande, Neelagandan Kamalanathan, Eswari Sampath, et al.
Hemoglobin|September 16, 2015
The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian AmazonAylla N L M Silva, Greice L Cardoso, Daniele A Cunha, et al.
Hemoglobin|October 20, 2015
Diagnosis of a Family with the Novel -α(21.9) Thalassemia DeletionJu Long, Wanrong Pang, Lei Sun, et al.
Hemoglobin|November 18, 2015
A Further Note on the Thalassemia Screening Program in the Muğla Region of TurkeyNejat Akar
Pageof 322