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Amrita Panja, Prosanto Chowdhury & Anupam Basu. (2016) Hb Midnapore [β53(D4)Ala→Val; HBB: c.161C>T]: A Novel Hemoglobin Variant with a Structural Abnormality Associated with IVS-I-5 (G>C) (HBB: c.92+5G>C) Found in a Bengali Indian Family. Hemoglobin 40:5, pages 300-303.
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S. Agarwal, M. Pradhan, U. R. Gupta, S. Samai & S. S. Agarwal. (2000) Geographic and Ethnic Distribution of β-Thalassemia Mutations in Uttar Pradesh, India. Hemoglobin 24:2, pages 89-97.
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Jeanne M. Rhea & Ross Molinaro. (2014) Pathology Consultation on HbA1c Methods and Interferences. American Journal of Clinical Pathology 141:1, pages 5-16.
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Juan R. Alvarez-Dominguez, Olga Amosova & Jacques R. Fresco. (2013) Self-catalytic DNA Depurination Underlies Human β-Globin Gene Mutations at Codon 6 That Cause Anemias and Thalassemias. Journal of Biological Chemistry 288:16, pages 11581-11589.
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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.
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Ilya Chumakov, Marta Blumenfeld, Oxana Guerassimenko, Laurent Cavarec, Marta Palicio, Hadi Abderrahim, Lydie Bougueleret, Caroline Barry, Hiroaki Tanaka, Philippe La Rosa, Anne Puech, Nadia Tahri, Annick Cohen-Akenine, Sylvain Delabrosse, Sébastien Lissarrague, Françoise-Pascaline Picard, Karelle Maurice, Laurent Essioux, Philippe Millasseau, Pascale Grel, Virginie Debailleul, Anne-Marie Simon, Dominique Caterina, Isabelle Dufaure, Kattayoun Malekzadeh, Maria Belova, Jian-Jian Luan, Michel Bouillot, Jean-Luc Sambucy, Gwenael Primas, Martial Saumier, Nadia Boubkiri, Sandrine Martin-Saumier, Myriam Nasroune, Hélène Peixoto, Arnaud Delaye, Virginie Pinchot, Mariam Bastucci, Sophie Guillou, Magali Chevillon, Ricardo Sainz-Fuertes, Said Meguenni, Joan Aurich-Costa, Dorra Cherif, Anne Gimalac, Cornelia Van Duijn, Denis Gauvreau, Gail Ouelette, Isabel Fortier, John Realson, Tatiana Sherbatich, Nadejda Riazanskaia, Evgeny Rogaev, Peter Raeymaekers, Jeroen Aerssens, Frank Konings, Walter Luyten, Fabio Macciardi, Pak C. Sham, Richard E. Straub, Daniel R. Weinberger, Nadine Cohen & Daniel Cohen. (2002)
Genetic and physiological data implicating the new human gene G72 and the gene for
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Sarita Agarwal, Y. Hattori & S.S. Agarwal. (2000) Rare ?-thalassemia mutations in Asian Indians. American Journal of Hematology 65:4, pages 322-323.
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