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Hemoglobin|August 21, 2013
Detection of Hb H disease genotypes common in northern Thailand by quantitative real-time polymerase chain reaction and high resolution melting analysesTeerapat Seeratanachot, Torpong Sanguansermsri, Dawan ShimbhuHemoglobin|October 12, 2013
Description of the phenotypes of 63 heterozygous, homozygous and compound heterozygous patients carrying the Hb Groene Hart [α119(H2)Pro→Ser; HBA1: c.358C>T] variantPhilippe Joly, Philippe Lacan, Caroline Garcia, et al.Hemoglobin|October 9, 2013
The risk of potential thromboembolic, renal and cardiac complications of sickle cell traitMatthew D Bucknor, Jeanna S Goo, Michael L CoppolinoHemoglobin|July 5, 2013
CODON 30 (-GAG) (α2): hematological parameters in heterozygotes and also patients with Hb H diseaseYu Yang, Dong-Zhi LiHemoglobin|July 18, 2013
A new high affinity variant Hb Aurillac (β141Leu→Val)Guilaine Boursier, Sébastien Trouillier, Muriel Giansily Blaizot, et al.Hemoglobin|November 1, 2011
Virtual learning using interactive multimedia-based tools for knowledge transfer and development of global patient care pathway in haemoglobinopathiesRekha Bajoria, Farrukh Shah, Charles H Rodeck, et al.Hemoglobin|March 6, 2012
Neonatal cyanosis due to a new (G)γ-globin variant causing low oxygen affinity: Hb F-Sarajevo [(G)γ102(G4)Asn→Thr, AAC>ACC]Urs Zimmermann-Baer, Ralph Capalo, Fabrizio Dutly, et al.Hemoglobin|March 6, 2012
Compound heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (Aγ81Leu-β86Ala) in a Ugandan womanZeqiu J Han, Cristina Lapuz, Jill F Rovenger, et al.Hemoglobin|March 6, 2012
Nonsense β-thalassemia mutation at codon 37 (TGG>TGA), detected for the first time in three Turkish casesSevcan Tug Bozdogan, Cagatay Unsal, Hakan Erkman, et al.Hemoglobin|July 28, 2015
Prevention of Hb Bart's (γ4) Disease Associated with the - -(THAI) α(0)-Thalassemia Deletion in Mainland ChinaDong-Zhi Li, Yan Li, Jian Li, et al.Pageof 240