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Hemoglobin
international journal for hemoglobin research
Volume 18, 1994 - Issue 3
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Original Article

Distribution of β-thalassemia mutations in three asian indian populations with distant geographical locations

E. Baysal Laboratory of Protein Chemistry and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
S. Sharma Laboratory of Protein Chemistry and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA; Department of Pathology, University College of Medical Sciences and Guru Teg Bahadur Hospital Shahdara, New Delhi, 110095, India
,
S. C. Wong Lee Hyson Laboratories Prince of Wales Hospital Shatin, New Territories, Hong Kong
,
V. B. Jogessar Department of Haematology, King Edward VIII Hospital, 4013, Durban, Republic of South Africa
&
T. H.J. Huisman Laboratory of Protein Chemistry and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
Pages 201-209 | Received 04 Jan 1994, Accepted 14 Mar 1994, Published online: 07 Jul 2009

Citations (19)

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Read on this site (8)

S. Marwah, A. Walls & A. D. Blann. (2012) Relationship between vitamin D and red blood cell indices in South Asians and White Europeans. British Journal of Biomedical Science 69:4, pages 182-185.
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Adel M. Abuzenadah, Ibtessam M. Ramzi Hussein, Ghazi A. Damanhouri, Faten M. A-Sayes, Mamdouh A. Gari, Adeel G. Chaudhary, Galila F. Zaher, Asma’a Al-Attas & Mohammad H. Al-Qahtani. (2011) Molecular Basis of β-Thalassemia in the Western Province of Saudi Arabia: Identification of Rare β-Thalassemia Mutations. Hemoglobin 35:4, pages 346-357.
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Anita Nadkarni, Takehisa Sakaguchi, Hiroshi Takaku, Ajit Gorakshakar, Supriya Phanasgaonkar, Roshan B. Colah, Dipika Mohanty & Ryoiti Kiyama. (2002) A NOVEL β0-THALASSEMIA MUTATION AT CODON 55 (−A) AND A RARE 17 bp DELETION AT CODONS 126–131 IN THE INDIAN POPULATION. Hemoglobin 26:1, pages 41-47.
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Georgi D. Efremov. (2001) FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999). Hemoglobin 25:2, pages 125-168.
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F. E. E. Vaz, C. B. Thakur(Mahadik)M. K. Banerjee & S. G. Gangal. (2000) Distribution of β-Thalassemia Mutations in the Indian Population Referred to a Diagnostic Center. Hemoglobin 24:3, pages 181-194.
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T. H. J. Huisman & M. F. H. Carver. (1998) The β-and -Thalassemia Repository (Ninth Edition; Part I). Hemoglobin 22:2, pages 169-195.
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H. Furuumi, N. Firdous, T. Inoue, H. Ohta, P. Winichagoon, S. Fucharoen & Y. Fukumaki. (1998) Molecular Basis of β-Thalassemia in the Maldives. Hemoglobin 22:2, pages 141-151.
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E. Baysal & M. F. H. Carver. (1995) The β- and δ-Thalassemia Repository (Eighth Edition). Hemoglobin 19:3-4, pages 213-236.
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Articles from other publishers (11)

Owen T. M. Chan, Kenneth D. Westover, Lisa Dietz, James L. Zehnder & Iris Schrijver. (2010) Comprehensive and Efficient HBB Mutation Analysis for Detection of β-Hemoglobinopathies in a Pan-Ethnic Population . American Journal of Clinical Pathology 133:5, pages 700-707.
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Marion Phylipsen, John F. Prior, Erna Lim, Neela Lingam, Ingrid P. Vogelaar, Piero C. Giordano, Jill Finlayson & Cornelis L. Harteveld. (2010) Thalassemia in Western Australia: 11 novel deletions characterized by Multiplex Ligation-dependent Probe Amplification. Blood Cells, Molecules, and Diseases 44:3, pages 146-151.
Crossref
Shirley Henderson, Adele Timbs, Janice McCarthy, Alice Gallienne, Margaretha Van Mourik, Gillian Masters, Alison May, Mohamed S.M. Khalil, Anna Schuh & John Old. (2009) Incidence of haemoglobinopathies in various populations — The impact of immigration. Clinical Biochemistry 42:18, pages 1745-1756.
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
Shahid Mahmood Baig, Ayesha Azhar, Hammad Hassan, Jamshaid Mahmood Baig, Muhammad Aslam, Mohammad Amin Ud Din, Javed Anver Qureshi & Tariq Zaman. (2006) Prenatal diagnosis of β‐thalassemia in Southern Punjab, Pakistan. Prenatal Diagnosis 26:10, pages 903-905.
Crossref
John Old. 2004. Genetic Disorders of the Indian Subcontinent. Genetic Disorders of the Indian Subcontinent 245 264 .
A.C. Gorakshakar, A.R. Pawar, A.H. Nadkarni, C.Y. Lu, D. Mohanty, R. Krishnamoorthy, C. Besmond & R.B. Colah. (1999) Potential of denaturing gradient gel electrophoresis for scanning of ?-thalassemia mutations in India. American Journal of Hematology 61:2, pages 120-125.
Crossref
Roshan Colah & Dipika Mohanty. (1998) β-Thalassemias : Expression, molecular mechanisms and mutations in Indians. The Indian Journal of Pediatrics 65:6, pages 815-823.
Crossref
A.R. Pawar, R.B. Colah & D. Mohanty. (1997) A Novel β+-Thalassemia Mutation (Codon 10 GCC → GCA) and a Rare Transcriptional Mutation (−28A → G) in Indians. Blood 89:10, pages 3888-3888.
Crossref
A.R. Pawar, R.B. Colah & D. Mohanty. (1997) A Novel β+-Thalassemia Mutation (Codon 10 GCC → GCA) and a Rare Transcriptional Mutation (−28A → G) in Indians. Blood 89:10, pages 3888-3888.
Crossref
Sürkü Tüzmen, A. Nazli Basak & Erol Baysal. (1997) Rare β-thalassemia mutation IVS-II-848 (C-A) first reported in a Turkish cypriot family. American Journal of Hematology 54:4, pages 338-339.
Crossref

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