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Hemoglobin
international journal for hemoglobin research
Volume 1, 1977 - Issue 7
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Original Article

Variation in Hemoglobin A2

F. Vella Department of Biochemistry, College of Medicine, University of Saskatchewan, Saskatoon, Sask., Canada, S7N OW0
Pages 619-650 | Received 23 May 1977, Accepted 26 Jul 1977, Published online: 07 Jul 2009

Citations (13)

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Read on this site (3)

Taner Karakaya, Fatma Silan & Ozturk Ozdemir. (2022) A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels. Hemoglobin 46:2, pages 87-90.
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Mohamed S.M. Khalil, Adele T. Timbs, Shirley J. Henderson, Anna Schuh & John M. Old. (2020) Twelve Cases of Hb Manitoba [α102(G9)Ser→Arg]: the Fluctuation in the Variant Expression. Hemoglobin 44:6, pages 442-445.
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John S. Waye, Barry Eng, Laurie Hellens, Betty-Ann Hohenadel, Lisa M. Nakamura & Lynda Walker. (2013) Normal Hb A2 β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C). Hemoglobin 37:2, pages 201-204.
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Articles from other publishers (10)

Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 261 324 .
Amer Wahed. 2019. Accurate Results in the Clinical Laboratory. Accurate Results in the Clinical Laboratory 321 327 .
Amer Wahed & Semyon Risin. 2013. Accurate Results in the Clinical Laboratory. Accurate Results in the Clinical Laboratory 295 304 .
D. ABDEL-GADIR, L. PHELAN & B. J. BAIN. (2009) Haemoglobin A 2 ′ and its significance in β thalassaemia diagnosis . International Journal of Laboratory Hematology 31:3, pages 315-319.
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Robert Van Kirk, Linda M. Sandhaus & James D. Hoyer. (2005) The Detection and Diagnosis of Hemoglobin A 2 ' by High-Performance Liquid Chromatography . American Journal of Clinical Pathology 123:5, pages 657-661.
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Maria De Angioletti, Giuseppina Lacerra, Carlo Gaudiano, Gabriella Mastrolonardo, Leonilde Pagano, Lucia Mastrullo, Santa Masciandaro & Clementina Carestia. (2002) Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features. Human Mutation 20:5, pages 358-367.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
P.F.R. LITTLE. 1981. Genetic Engineering. Genetic Engineering 61 102 .
F Vella. (1980) Human haemoglobins and molecular disease. Biochemical Education 8:2, pages 41-53.
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M. Marinucci, F. Mavilio, A. Massa, M. Gabbianelli, P. P. Fontanarosa, P. Samoggia & L. Tentori. (2008) Haemoglobin Lepore Trait: Haematological and Structural Studies on the Italian Population. British Journal of Haematology 42:4, pages 557-565.
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