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Hemoglobin|November 28, 2012
α0-Thalassemia trait with normal red cell indices: a report of two casesCan Liao, Dong-Zhi LiHemoglobin|December 11, 2012
The spectrum of α-thalassemia mutations in the Kurdish population of Northeastern IraqNasir A S Al-Allawi, Sana D Jalal, Najeeb S Rasheed, et al.Hemoglobin|February 24, 2012
Simultaneous detection of Hb constant spring (α142, TAA>CAA, α2) and the α2 IVS-I donor site (-TGAGG) deletion by a simple polymerase chain reaction-based method in IranHaleh Akhavan-Niaki, Ali Banihashemi, Amrollah Mostafazadeh, et al.Hemoglobin|September 16, 2014
Adult sickle cell disease epidemiology and the potential role of a multidisciplinary comprehensive care center in a city with low prevalenceAndrew Binding, Karen Valentine, Man-Chiu Poon, et al.Hemoglobin|September 20, 2014
Primary stroke in a woman with sickle cell anemia responsive to hydroxyurea therapySamir K Ballas, Ubaldo Martinez, Michael SavageHemoglobin|October 2, 2014
Two new γ chain variants: Hb F-Augusta GA [(G)γ59(E3)Lys → Arg; HBG2: c.179A > G] and Hb F-Port Royal-II [(A)γ125(H3)Glu → Ala; HBG1: c.377A > C]Ferdane Kutlar, Afshin Ameri, Niren H Patel, et al.Hemoglobin|June 4, 2013
Polymorphism in the HMOX1 gene is associated with high levels of fetal hemoglobin in Brazilian patients with sickle cell anemiaGislene P Gil, Galina Ananina, Mariana B Oliveira, et al.Hemoglobin|June 29, 2013
Two complex associations of an HBD mutation and a rare α hemoglobinopathyPhilippe Joly, Philippe Lacan, Caroline Garcia, et al.Hemoglobin|November 9, 2013
Hemoglobin analyses in the Netherlands reveal more than 80 different variants including six novel onesRob van Zwieten, Martijn Veldthuis, Barend Delzenne, et al.Hemoglobin|January 1, 1986
Association of the level of G gamma chain in the fetal hemoglobin of normal adults with specific haplotypesY Hattori, F Kutlar, C J Mosley, et al.Pageof 240