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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 EngHemoglobin|February 12, 2009
Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG)Barry Eng, Lynda Walker, John S WayeRespiratory Medicine|August 9, 2005
Repeatability of standardised nasal nitric oxide measurements in healthy and asthmatic adults and childrenSergei A Kharitonov, Lynda Walker, Peter J BarnesHemoglobin|December 24, 2005
High Hb A2 beta-thalassemia due to a 468 bp deletion in a patient with Hb S/beta-thalassemiaMargie Patterson, Lynda Walker, Barry Eng, et al.Hemoglobin|March 17, 2007
High oxygen affinity hemoglobin variant in a Canadian family: Hb Bunbury [beta94(FG1)Asp-->Asn, GAC-->AAC]Lynda Walker, Barry Eng, Andrew McFarlane, et al.Hemoglobin|December 24, 2005
Identification of a new delta chain hemoglobin variant in a beta-thalassemia carrier: Hb A2-mumc [delta13(a10)Ala-->Asp]Lynda Walker, Margie Patterson, Barry Eng, et al.Hemoglobin|December 24, 2005
Characterization of a rare single alpha-globin gene deletion in a Chinese woman with Hb H diseaseBarry Eng, Robert Walsh, Lynda Walker, et al.Hemoglobin|February 12, 2009
Hb North York [beta 117(G19)His-->Asp]: a new beta chain hemoglobin variantJohn S Waye, Lynda Walker, Lisa M Nakamura, et al.Hemoglobin|November 29, 2017
Characterization of Two Novel Deletions Involving the 5' Region of the β-Globin GeneJohn S Waye, Meredith Hanna, Betty-Ann Hohenadel, et al.Hemoglobin|November 9, 2016
Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A)John S Waye, Barry Eng, Meredith Hanna, et al.Pageof 3