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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 2
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Original Article

Geographic and Ethnic Distribution of β-Thalassemia Mutations in Uttar Pradesh, India

S. Agarwal Department of Medical Genetics, Sanjay Gandhi Post-Graduate Institute of Medical Sciences, Lucknow, 226014, IndiaCorrespondence[email protected]
,
M. Pradhan Department of Medical Genetics, Sanjay Gandhi Post-Graduate Institute of Medical Sciences, Lucknow, 226014, India
,
U. R. Gupta Department of Medical Genetics, Sanjay Gandhi Post-Graduate Institute of Medical Sciences, Lucknow, 226014, India
,
S. Samai Department of Medical Genetics, Sanjay Gandhi Post-Graduate Institute of Medical Sciences, Lucknow, 226014, India
&
S. S. Agarwal Department of Medical Genetics, Sanjay Gandhi Post-Graduate Institute of Medical Sciences, Lucknow, 226014, India
Pages 89-97 | Received 28 Jul 1999, Accepted 04 Nov 1999, Published online: 07 Jul 2009

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Roshan B. Colah, Anita H. Nadkarni, Ajit C. Gorakshakar, Pratibha M. Sawant, Pallavi R. Mehta, Manju S. Gorivale, Priya Hariharan, Dipika Mohanty & Kanjaksha Ghosh. (2021) The Changing Trends in Prenatal Diagnosis of Hemoglobinopathies in India: The Quest of a Single Center to Reduce the Burden of Disease over Three Decades. Hemoglobin 45:2, pages 112-118.
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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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Hossam Murad, Faten Moasses, Amir Dabboul, Yasser Mukhalalaty, Ahmad Omar Bakoor, Walid Al-Achkar & Rami A. Jarjour. (2018) Geographical distribution of β-globin gene mutations in Syria. Hematology 23:9, pages 697-704.
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Aditya N. Jha, Hrishikesh Mishra, Henu K. Verma, Isha Pandey & Bhaskar V.K.S. Lakkakula. (2018) Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India. Hemoglobin 42:2, pages 84-90.
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Slaheddine Fattoum, Taeib Messaoud & Amina Bibi. (2004) Molecular Basis of β‐Thalassemia in the Population of Tunisia. Hemoglobin 28:3, pages 177-187.
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Guru Prasad Chhotray, Bisnu Prasad Dash & Manoranjan Ranjit. (2004) Spectrum of Hemoglobinopathies in Orissa, India. Hemoglobin 28:2, pages 117-122.
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Ajit C. Gorakshakar, Supriya P. Phanasgaonkar, Anita H. Nadkarni, Roshan B. Colah & Dipika Mohanty. (2004) Detection of Rare β‐Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians. Hemoglobin 28:1, pages 15-24.
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Sarita Agarwal, Swati Sarwai, Savita Agarwal, Usha R. Gupta & Shubha Phadke. (2002) THALASSEMIA INTERMEDIA: HETEROZYGOUS β-THALASSEMIA AND CO-INHERITANCE OF AN α GENE TRIPLICATION. Hemoglobin 26:3, pages 321-323.
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Articles from other publishers (21)

Ekta Rao, Sandip Kumar Chandraker, Mable Misha Singh & Ravindra Kumar. (2024) Global distribution of β-thalassemia mutations: An update. Gene 896, pages 148022.
Crossref
Poonam Tripathi, Sarita Agarwal, Anshul Gupta & Kausik Mandal. (2020) Biallelic rare 17 bp deletion mutation (HBB:c.380_396 del TGCAGGCTGCCTATCAG) in a transfusion depended form of thalassemia. Annals of Hematology 99:11, pages 2719-2722.
Crossref
P. Tripathi, S. Muthuswamy & S. Agarwal. (2017) A novel single nucleotide deletion mutation in exon 2 ( HBB : c240delC) of beta globin gene: A case report . International Journal of Laboratory Hematology 39:6.
Crossref
Rachana Nagar, Sujata Sinha & Rajiva Raman. (2015) Genotype–phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients. Blood Cells, Molecules, and Diseases 55:1, pages 10-14.
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Shagun Aggarwal & Shubha R Phadke. (2015) Medical genetics and genomic medicine in India: current status and opportunities ahead. Molecular Genetics & Genomic Medicine 3:3, pages 160-171.
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Ravindra Kumar, Vandana Arya & Sarita Agarwal. (2015) Profiling β Thalassemia Mutations in Consanguinity and Nonconsanguinity for Prenatal Screening and Awareness Programme . Advances in Hematology 2015, pages 1-5.
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Rachana Nagar, Sujata Sinha & Rajiva Raman. (2014) Haemoglobinopathies in eastern Indian states: a demographic evaluation. Journal of Community Genetics 6:1, pages 1-8.
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Ravindra Kumar, Anupriya Kaur & Sarita Agarwal. (2013) Influence of Xmn 1Gγ (HBG2 c.-211 C → T) Globin Gene Polymorphism on Phenotype of Thalassemia Patients of North India. Indian Journal of Hematology and Blood Transfusion 30:4, pages 286-290.
Crossref
Gururaj D. KulkarniSuyamindra S. KulkarniGurushantappa S. KadakolBhushan B. KulkarniPrakashgouda H. KyamangoudarBhaskar V.K.S. LakkakulaKumarasamy ThangarajTipperudra A. ShepurMuralidhar L. KulkarniPramod B. Gai. (2012) Molecular Basis of β-Thalassemia in Karnataka, India. Genetic Testing and Molecular Biomarkers 16:2, pages 138-141.
Crossref
Ali Reza Rezaee, Mohammad Mehdi Banoei, Elham Khalili & Massoud Houshmand. (2012) Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration. The Scientific World Journal 2012, pages 1-7.
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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.
Crossref
S. Sinha, M. L. Black, S. Agarwal, R. Colah, R. Das, K. Ryan, M. Bellgard & A. H. Bittles. (2010) Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes. The HUGO Journal 3:1-4, pages 51-62.
Crossref
Roshan Colah, Ajit Gorakshakar, Anita Nadkarni, Supriya Phanasgaonkar, Reema Surve, Pratibha Sawant, Dipika Mohanty & Kanjaksha Ghosh. (2009) Regional heterogeneity of β-thalassemia mutations in the multi ethnic Indian population. Blood Cells, Molecules, and Diseases 42:3, pages 241-246.
Crossref
Sarita Agarwal, D. Tewari, V. Arya, N. Moorchung, R. Tripathi, G. Chaudhuri & M. Pradhan. (2007) Status of HFE mutation in thalassemia syndromes in north India. Annals of Hematology 86:7, pages 483-485.
Crossref
Sarita Agarwal, Vandana Arya, Catherine A. Stolle & Mandakini Pradhan. (2006) A novel Indian ?-thalassemia mutation in the CACCC box of the promoter region. European Journal of Haematology 77:6, pages 530-532.
Crossref
Vaikam H. Sankar, Vandana Arya, Depshikha Tewari, Usha R. Gupta, Mandakini Pradhan & Sarita Agarwal. (2006) Genotyping of alpha-thalassemia in microcytic hypochromic anemia patients from North India. Journal of Applied Genetics 47:4, pages 391-395.
Crossref
Partha Chakrabarti, Ramkrishna Gupta, Ashutosh Mishra, Madhukar Rai, Vijay Pratap Singh & Debabrata Dash. (2005) Spectrum of β-thalassemia mutations in North Indian states: A β-thalassemia trait with two mutations in cis. Clinical Biochemistry 38:6, pages 576-578.
Crossref
John Old. 2004. Genetic Disorders of the Indian Subcontinent. Genetic Disorders of the Indian Subcontinent 245 264 .
Anju Gupta, Yukio Hattori, Usha R. Gupta, Swati Sarwai, Nitu Nigam, Pragya Singhal & Sarita Agarwal. (2003) Molecular Genetic Testing of β-Thalassemia Patients of Indian Origin and a Novel 8-bp Deletion Mutation at Codons 36/37/38/39. Genetic Testing 7:2, pages 163-168.
Crossref
Anju Gupta, Yukio Hattori & Sarita Agarwal. (2002) Initiation codon mutation in an Asian Indian family. American Journal of Hematology 71:2, pages 134-136.
Crossref
Sarita Agarwal, Y. Hattori & S.S. Agarwal. (2000) Rare ?-thalassemia mutations in Asian Indians. American Journal of Hematology 65:4, pages 322-323.
Crossref

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