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Hemoglobin
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January 26, 2012
Comparison of two known chromosomal rearrangements in the δβ-globin complex with identical DNA breakpoints but causing different Hb A(2) levels
Elisabeth Saller, Kamran Moradkhani, Fabrizio Dutly, et al.
Hemoglobin
|
January 1, 1990
Hb Lepore-Baltimore in a north Sardinian family
B Masala, L Manca, J B Wilson, et al.
Hemoglobin
|
January 14, 2012
Prenatal diagnosis of hemoglobinopathies by pyrosequencing: a more sensitive and rapid approach to fetal genotyping
Adele T Timbs, Michelle J Rugless, Alice E Gallienne, et al.
Hemoglobin
|
January 14, 2012
Screening for common nondeletional α-thalassemias in Chinese newborns by determination of Hb Bart's using the Sebia Capillarys 2 electrophoresis system
Hai-Shen Tang, Jian-Ying Zhou, Xing-Mei Xie, et al.
Hemoglobin
|
March 29, 2012
Microsatellite markers within the α-globin gene cluster for robust preimplantation genetic diagnosis of severe α-thalassemia syndromes in Mediterranean populations
Aspasia Destouni, George Christopoulos, Christina Vrettou, et al.
Hemoglobin
|
March 24, 2012
Proceedings of the International Conference on Hemoglobin Disorders, February 5-7th, 2011, Kuwait. In memoriam of T.H.J. Huisman
Hemoglobin
|
March 22, 2012
A novel case of Hb Phnom Penh: codons 117/118 (+ATC) as a cause of α+ -thalassemia
Yin-Sheng Zhai, Hai-Shen Tang, Jian-Ying Zhou, et al.
Hemoglobin
|
November 30, 2011
Novel α2 gene deletion (c.349_359 del GAGTTCACCCC) identified in association with the -α3.7 deletion
Stephen O Brennan, Tim Chan, Jaine Duncan
Hemoglobin
|
April 10, 2012
Coenzyme Q10 levels in β-thalassemia and its association with ferritin levels and chelation therapy
Cigdem Karakukcu, Musa Karakukcu, Ekrem Unal, et al.
Hemoglobin
|
March 2, 2012
α(+)-Thalassemia trait caused by a frameshift mutation in exon 2 of the α2-globin gene [HBA2 c.244delT]
John S Waye, Lynda Walker, Barry Eng
Page
of 322
Search research articles
Search
Showing results (381-390 of 3,216) with videos related to
Sort By:
Page
of 322
Hemoglobin
|
January 26, 2012
Comparison of two known chromosomal rearrangements in the δβ-globin complex with identical DNA breakpoints but causing different Hb A(2) levels
Elisabeth Saller, Kamran Moradkhani, Fabrizio Dutly, et al.
Hemoglobin
|
January 1, 1990
Hb Lepore-Baltimore in a north Sardinian family
B Masala, L Manca, J B Wilson, et al.
Hemoglobin
|
January 14, 2012
Prenatal diagnosis of hemoglobinopathies by pyrosequencing: a more sensitive and rapid approach to fetal genotyping
Adele T Timbs, Michelle J Rugless, Alice E Gallienne, et al.
Hemoglobin
|
January 14, 2012
Screening for common nondeletional α-thalassemias in Chinese newborns by determination of Hb Bart's using the Sebia Capillarys 2 electrophoresis system
Hai-Shen Tang, Jian-Ying Zhou, Xing-Mei Xie, et al.
Hemoglobin
|
March 29, 2012
Microsatellite markers within the α-globin gene cluster for robust preimplantation genetic diagnosis of severe α-thalassemia syndromes in Mediterranean populations
Aspasia Destouni, George Christopoulos, Christina Vrettou, et al.
Hemoglobin
|
March 24, 2012
Proceedings of the International Conference on Hemoglobin Disorders, February 5-7th, 2011, Kuwait. In memoriam of T.H.J. Huisman
Hemoglobin
|
March 22, 2012
A novel case of Hb Phnom Penh: codons 117/118 (+ATC) as a cause of α+ -thalassemia
Yin-Sheng Zhai, Hai-Shen Tang, Jian-Ying Zhou, et al.
Hemoglobin
|
November 30, 2011
Novel α2 gene deletion (c.349_359 del GAGTTCACCCC) identified in association with the -α3.7 deletion
Stephen O Brennan, Tim Chan, Jaine Duncan
Hemoglobin
|
April 10, 2012
Coenzyme Q10 levels in β-thalassemia and its association with ferritin levels and chelation therapy
Cigdem Karakukcu, Musa Karakukcu, Ekrem Unal, et al.
Hemoglobin
|
March 2, 2012
α(+)-Thalassemia trait caused by a frameshift mutation in exon 2 of the α2-globin gene [HBA2 c.244delT]
John S Waye, Lynda Walker, Barry Eng
Page
of 322