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Hemoglobin
international journal for hemoglobin research
Volume 32, 2008 - Issue 5
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Short Communications

Polymerase Chain Reaction-Based Search for Two α-Globin Gene Mutations in India

Gargi Bhattacharya Department of Bio-Physics, Molecular Biology & Genetics, University of Calcutta, Kolkata, India
,
Anjali A. Sarkar Department of Bio-Physics, Molecular Biology & Genetics, University of Calcutta, Kolkata, India
,
Debasish Banerjee Park Clinic, Kothari Medical Centre, Kolkata, India
,
Sarmila Chandra Department of Haematology, Kothari Medical Centre, Kolkata, India
,
Manikanchan Das Department of Haematology, Kothari Medical Centre, Kolkata, India
&
Uma B. Dasgupta Department of Bio-Physics, Molecular Biology & Genetics, University of Calcutta, Kolkata, IndiaCorrespondence[email protected] [email protected]
Pages 485-490 | Received 22 Oct 2007, Accepted 06 Mar 2008, Published online: 07 Jul 2009

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Pacharapan Surapolchai, Nongnuch Sirachainan, Chi-Chiu So, Suradej Hongeng, Samart Pakakasama, Usanarat Anurathapan & Ampaiwan Chuansumrit. (2016) Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses. Hemoglobin 40:1, pages 70-73.
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Divya Jayasree, Ramachandran V. Shaji, Biju George, Vikram Mathews, Alok Srivastava & Eunice S. Edison. (2016) Clinical, Hematological and Molecular Analysis of Homozygous Hb E (HBB: c.79G > A) in the Indian Population. Hemoglobin 40:1, pages 16-19.
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Prashant Deshpande, Neelagandan Kamalanathan, Eswari Sampath, Biju George, Ramachandran V. Shaji & Eunice S. Edison. (2015) Characterization of Clinical and Laboratory Profiles of the Deletional α2-Globin Gene Polyadenylation Signal Sequence (AATAAA > AATA– –) in an Indian Population. Hemoglobin 39:6, pages 415-418.
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Sona B. Nair, Anita H. Nadkarni, Kanjaksha Ghosh & Roshan B. Colah. (2013) Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A TIndian (AATAAA>AATA– –) Mutation in Four Indian Families. Hemoglobin 37:3, pages 277-284.
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Papai Roy, Gargi Bhattacharya, Debasish Banerjee, Sarmila Chandra, Malay Ghosh, Utpal Choudhuri, Manikanchan Das & Uma B. Dasgupta. (2009) Hb Sallanches [α104(G11)Cys→Tyr, TGC>TAC] Occurs Frequently on the Indian Subcontinent. Hemoglobin 33:6, pages 486-491.
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Articles from other publishers (3)

Pallavi Thaker, Namrata Mahajan, Malay B. Mukherjee & Roshan B. Colah. (2022) Molecular Heterogeneity of Hb H Disease in India. Thalassemia Reports 12:3, pages 73-84.
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Ankur Jain, Pooja Prasad, Sumita Chaudhry, D.K. Gupta & Sumita Saluja. (2021) Hb Sun Prairie: A rare cause of chronic hemolysis in an Indian patient. Hematology/Oncology and Stem Cell Therapy 14:3, pages 257-259.
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Anita H. Nadkarni, Ajit C. Gorakshakar, Pratibha M. Sawant, Khushnooma Y. Italia, Dipti S. Upadhye, Manju S. Gorivale, Pallavi R. Mehta, Priya Hariharan, Kanjaksha Ghosh & Roshan B. Colah. (2018) The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral center. International Journal of Laboratory Hematology 41:2, pages 218-226.
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