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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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Preetinanda M. Dash, Praveen K. Sahu, Siris Patel, Ranjeet S. Mashon, Kiran R. Kharat & Malay B. Mukherjee. (2018) Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia. Hemoglobin 42:4, pages 236-242.
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Anuradha V. Shrikhande, Aishwarya Arjunan, Amit Agarwal, Aarti Dani, Jayashri Tijare, Elizabeth Gettig & Lakshmanan Krishnamurti. (2014) Prevalence of the βS Gene Among Scheduled Castes, Scheduled Tribes and Other Backward Class Groups in Central India. Hemoglobin 38:4, pages 230-235.
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Subhransu Sekhar Sahoo, Sebaranjan Biswal & Manjusha Dixit. (2014) Distinctive Mutation Spectrum of the HBB Gene in an Urban Eastern Indian Population. Hemoglobin 38:1, pages 33-38.
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Sudhansu Sekhar Nishank, Manoranjan Ranjit, Shantanu K. Kar & Guru Prasad Chhotray. (2009) Molecular variants and clinical importance of β-thalassaemia traits found in the state of Orissa, India. Hematology 14:5, pages 290-296.
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Sudhansu Sekhar Nishank, Manoranjan Ranjit & Guru Prasad Chhotray. (2008) First report of a nonsense mutation at codon 15(TGG→TAG) in exon 1 of the β globin gene in a β thalassemia trait in State of Orissa, India. Hematology 13:1, pages 65-67.
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R. S. Balgir. (2005) The spectrum of haemoglobin variants in two scheduled tribes of Sundargarh district in north-western Orissa, India. Annals of Human Biology 32:5, pages 560-573.
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Articles from other publishers (12)
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Sujata Dixit, Arundhuti Das, Ramakanta Rana, Hemant K. Khuntia, Akhil B. Ota, Sanghamitra Pati, Madhusmita Bal & Manoranjan Ranjit. (2022) A community based study on haemoglobinopathies and G6PD deficiency among particularly vulnerable tribal groups in hard-to-reach malaria endemic areas of Odisha, India: implications on malaria control. Malaria Journal 21:1.
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Dhriti Sundar Das & Debananda Sahoo. (2020) Coevality of Systemic Lupus Erythematosus With Sickle Cell Trait: A Not So Uncommon Entity. Cureus.
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H P S Sachdev & T Gera. (2013) Preventing childhood anemia in India: iron supplementation and beyond. European Journal of Clinical Nutrition 67:5, pages 475-480.
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D. Mohanty, R. B. Colah, A. C. Gorakshakar, R. Z. Patel, D. C. Master, J. Mahanta, S. K. Sharma, U. Chaudhari, M. Ghosh, S. Das, R. P. Britt, S. Singh, C. Ross, L. Jagannathan, R. Kaul, D. K. Shukla & V. Muthuswamy. (2012) Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study. Journal of Community Genetics 4:1, pages 33-42.
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Ravindra Kumar, Inusha Panigrahi, Ashwin Dalal & Sarita Agarwal. (2011) Sickle Cell Anemia—Molecular Diagnosis and Prenatal Counseling: SGPGI Experience. The Indian Journal of Pediatrics 79:1, pages 68-74.
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Vineeta Gupta, Jyoti Shukla, Vijai Tilak & Baldev Bhatia. (2009) Spectrum of hemoglobinopathies in Eastern Uttar Pradesh. The Indian Journal of Pediatrics 76:8, pages 857-857.
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Daniel David Mais, Ronald D. Gulbranson & David F. Keren. (2009) The Range of Hemoglobin A2 in Hemoglobin E Heterozygotes as Determined by Capillary Electrophoresis. American Journal of Clinical Pathology 132:1, pages 34-38.
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