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Hemoglobin
international journal for hemoglobin research
Volume 5, 1981 - Issue 6
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Original Article

Hemoglobin A2 in Iron Deficient 8-Thalassemia Heterozygotes

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Pages 613-618 | Received 18 Aug 1980, Accepted 23 Feb 1981, Published online: 07 Jul 2009

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Read on this site (4)

Saeed Anwar, Jarin Taslem Mourosi, Md. Kamrul Hasan, Mohammad Jakir Hosen & Md. Faruque Miah. (2020) Umbilical Cord Blood Screening for the Detection of Common Deletional Mutations of α-Thalassemia in Bangladesh. Hemoglobin 44:3, pages 201-210.
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Suha M. Hassan, Cornelis L. Harteveld, Egbert Bakker & Piero C. Giordano. (2014) Known and New δ-Globin Gene Mutations and Other Factors Influencing Hb A2 Measurement in the Omani Population. Hemoglobin 38:4, pages 299-302.
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J. M. Old. (2007) Screening and genetic diagnosis of haemoglobinopathies. Scandinavian Journal of Clinical and Laboratory Investigation 67:1, pages 71-86.
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Articles from other publishers (16)

Noraesah Mahmud, Massimo Maffei, Massimo Mogni, Gian Luca Forni, Valeria Maria Pinto, Giuseppina Barberio, Silvana Ungari, Antonella Maffè, Cristina Curcio, Francesco Zanolli, Raffaella Paventa, Mariarosa Carta, Alberta Caleffi, Mariella Mercadanti, Sauro Maoggi, Giovanni Ivaldi & Domenico Coviello. (2021) Hemoglobin A2 and Heterogeneous Diagnostic Relevance Observed in Eight New Variants of the Delta Globin Gene. Genes 12:11, pages 1821.
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Stacy Colaco & Anita Nadkarni. (2021) Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers. Mutation Research/Reviews in Mutation Research 788, pages 108387.
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Farjana Akther Noor, Nusrat Sultana, Golam Sarower Bhuyan, Md Tarikul Islam, Mohabbat Hossain, Suprovath Kumar Sarker, Khaleda Islam, Waqar Ahmed Khan, Mujahida Rahman, Syeda Kashfi Qadri, Hossain Uddin Shekhar, Firdausi Qadri, Syed Saleheen Qadri & Kaiissar Mannoor. (2020) Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population. Orphanet Journal of Rare Diseases 15:1.
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Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 85 184 .
Md Tarikul Islam, Suprovath Kumar Sarkar, Nusrat Sultana, Mst. Noorjahan Begum, Golam Sarower Bhuyan, Shezote Talukder, A. K. M. Muraduzzaman, Md Alauddin, Mohammad Sazzadul Islam, Pritha Promita Biswas, Aparna Biswas, Syeda Kashfi Qadri, Tahmina Shirin, Bilquis Banu, Salma Sadya, Manzoor Hussain, Golam Sarwardi, Waqar Ahmed Khan, Mohammad Abdul Mannan, Hossain Uddin Shekhar, Emran Kabir Chowdhury, Abu Ashfaqur Sajib, Sharif Akhteruzzaman, Syed Saleheen Qadri, Firdausi Qadri & Kaiissar Mannoor. (2018) High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh. BMC Genetics 19:1.
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Andrew Turner, Jurgen Sasse & Aniko Varadi. (2016) Rapid detection of pathological mutations and deletions of the haemoglobin beta gene (HBB) by High Resolution Melting (HRM) analysis and Gene Ratio Analysis Copy Enumeration PCR (GRACE-PCR). BMC Medical Genetics 17:1.
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Lucia Perseu, Stefania Satta, Paolo Moi, Franca Rosa Demartis, Laura Manunza, Maria Carla Sollaino, Susanna Barella, Antonio Cao & Renzo Galanello. (2011) KLF1 gene mutations cause borderline HbA2. Blood 118:16, pages 4454-4458.
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Barbara J. Bain, Barbara J. Wild, Adrian D. Stephens & Lorraine A. Phelan. 2010. Variant Haemoglobins. Variant Haemoglobins 57 71 .
. 2006. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 63 138 .
Antonio Cao. (2002) Carrier screening and genetic counselling in β-thalassemia. International Journal of Hematology 76:S2, pages 105-113.
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Antonio Cao & Paolo Moi. (2000) Genetic Modifying Factors in β-Thalassemia. cclm 38:2, pages 123-132.
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Antonio Cao, Renzo Galanello & M. Cristina Rosatelli. (1998) 8 Prenatal diagnosis and screening of the haemoglobinopathies. Baillière's Clinical Haematology 11:1, pages 215-238.
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A. Cao, R. Galanello & M.C. Rosatelli. (1994) Genotype-phenotype correlations in β-thalassemias. Blood Reviews 8:1, pages 1-12.
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Martin H. Steinberg. (1993) Case Report: Effects of Iron Deficiency and the-88C→T Mutation on HbA2 Levels in β-thalassemia. The American Journal of the Medical Sciences 305:5, pages 312-313.
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Antonio Cao & Maria Cristina Rosatelli. (1993) 9 Screening and prenatal diagnosis of the haemoglobinopathies. Baillière's Clinical Haematology 6:1, pages 263-286.
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M C Willcox, J Liljestrand & S Bergstrom. (1986) Abnormal haemoglobins among pregnant women from Mozambique.. Journal of Medical Genetics 23:2, pages 151-152.
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