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Hemoglobinopathy

Molecular variants and clinical importance of β-thalassaemia traits found in the state of Orissa, India

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Pages 290-296 | Published online: 18 Jul 2013

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Snehadhini Dehury, Satyabrata Meher, Siris Patel, Kishalaya Das, Arpita Jana, Subhra Bhattacharya, Sarmila Sahoo, Biswanath Sarkar & Pradeep K. Mohanty. (2019) Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India. Hemoglobin 43:2, pages 132-136.
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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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Articles from other publishers (4)

H. Ben Hamouda, B. Mahjoub, H. Soua, S. Laradi, A. Miled & M.T. Sfar. (2017) Expression néonatale d’un trait bêta-thalassémique associé à une sphérocytose héréditaire chez deux jumelles monozygotes. Archives de Pédiatrie 24:2, pages 126-130.
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Ranbir S. Balgir. (2014) Reproductive Outcome in Carrier Couples of β-Thalassemia Disorders in a Tertiary Hospital in Central India. Thalassemia Reports 4:1, pages 1907.
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M. L. Black, S. Sinha, S. Agarwal, R. Colah, R. Das, M. Bellgard & A. H. Bittles. (2010) A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka. Journal of Community Genetics 1:3, pages 149-157.
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Roshan Colah, Ajit Gorakshakar, Supriya Phanasgaonkar, Edna D’Souza, Anita Nadkarni, Reema Surve, Pratibha Sawant, Dilip Master, Ramesh Patel, Kanjaksha Ghosh & Dipika Mohanty. (2010) Epidemiology of β-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat. British Journal of Haematology 149:5, pages 739-747.
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