Glycine

hemoglobin subunit alpha 2 ; Homo sapiens







12 Article(s)
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1 26583619 Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-Thalassemia. 2016 Jan 1
2 27686733 Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -SEA/) Deletion. 2016 Sep 1
3 24905386 Rare hemoglobin variants in Tunisian population. 2015 Apr 1
4 25858298 Fortuitous description of haemoglobin A2' [δ16 (A13) Gly→Arg (GGC→CGC)] in a Tunisian family: study of the molecular defect and its origin. 2015 May-Jun 1
5 23806011 Two complex associations of an HBD mutation and a rare α hemoglobinopathy. 2013 1
6 21417576 Identification of a new α chain variant at codons 22-25 (-9 nts) using the Sebia capillarys 2 electrophoresis system. 2011 1
7 21466672 An insight into the suspected HbA2' cases detected by high performance liquid chromatography in Pakistan. 2011 Apr 5 1
8 18601605 The silent hemoglobin alpha chain variant Hb Riccarton [alpha51(CE9)Gly-->Ser] may affect HbA1c determination on the HLC-723 G7 analyzer. 2008 1
9 18654886 A rare thalassemic syndrome caused by interaction of Hb Adana [alpha59(E8)Gly-->Asp] with an alpha+-thalassemia deletion: clinical aspects in two cases. 2008 1
10 12908799 Hb Bronte or alpha93(FG5)Val-->Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotype. 2003 Aug 1
11 9101295 delta-Thalassemic phenotype due to two "novel" delta-globin gene mutations: CD11[GTC-->GGC (A8)-HbA2-Pylos] and CD 85[TTT-->TCT(F1)-HbA2-Etolia]. 1997 1
12 1176817 Microchromatography of hemoglobins. II. A simplified procedure for the determination of hemoglobin A2. 1975 Oct 1