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Hemoglobin|December 5, 2009
Southeast Asian ovalocytosis and a sickle cell trait in a young patient with sudden retinal stroke: a fortuitous association?Fabrizia Favale, Martine Gardembas, Olivier Pajot, et al.Hemoglobin|December 5, 2009
HB Fannin-Lubbock-I with a single GGC>GAC mutation at beta119(GH2)Gly-->Asp in a homozygous Mexican patientBertha Ibarra, Edna Aizpuru, J Yoaly Sánchez-López, et al.Hemoglobin|December 5, 2009
Hb Alperton [beta135(H13)Ala-->Val] shows decreased oxygen affinityKarin Zurbriggen, Marlis Schmid, Markus Schmugge, et al.Hemoglobin|December 5, 2009
HB Hillingdon [alpha46(CE4)Phe-->Val (alpha1 Or alpha2)]: a new alpha chain hemoglobin variantAnna Babb, Susannah Solaiman, Brian N Green, et al.Hemoglobin|December 5, 2009
Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancyNirut Siriratmanawong, Wichuda Chansri, Sanita Singsanan, et al.Hemoglobin|January 1, 1992
Rapid molecular diagnosis of hemoglobin variants by RT-PCR of reticulocyte mRNA and direct sequencingT C Liu, J S Yen, J S Shen, et al.Hemoglobin|April 10, 2002
Hb O-Tibesti [beta121(GH4)Glu-->Lys; beta11(A8)Val-->Ile], a hemoglobin variant carrying in the same beta chain the substitutions of Hb O-Arab and Hb Hamilton, found in combination with Hb S [beta6(A3)Glu-->Val]Claude Préhu, Jean Riou, Isabelle Sartelet, et al.Hemoglobin|April 10, 2002
A novel beta-thalassemia mutation in an Asian IndianRamachandran V Shaji, Nathalie Gerard, Rajagopal Krishnamoorthy, et al.Hemoglobin|October 1, 2014
A new β(0) frameshift mutation, HBB: c.44delT (p.Leu14ArgfsX5), identified in an Argentinean family associated with secondary genetic modifiers of β-thalassemiaCarolina Pepe, Silvia Eandi Eberle, Alejandro Chaves, et al.Hemoglobin|October 2, 2014
Priapism, an emerging complication in β-thalassemia intermedia patientsNaji S Mallat, David Wehbe, Anthony Haddad, et al.Pageof 239