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Citation: A. Nadkarni et al., Molecular pathogenesis and clinical variability of beta-thalassemia syndromes among Indians, AM J HEMAT, 68(2), 2001, pp. 75-80

Authors: Mukherjee, MB Surve, RR Gorakshakar, AC Gangakhedkar, RR Colah, RB Mohanty, D

Citation: Mb. Mukherjee et al., Symptomatic presentation of a sickle cell heterozygote: An evaluation of genetic factors, AM J HEMAT, 66(4), 2001, pp. 307-308

Authors: Murhekar, KM Murhekar, MV Mukherjee, MB Gorakshakar, AC Surve, R Wadia, M Phanasgaonkar, S Shridevi, S Roshan, BC Mohanty, D

Citation: Km. Murhekar et al., Red cell genetic abnormalities, beta-globin gene haplotypes, and APOB polymorphism in the Great Andamanese, a primitive Negrito tribe of Andaman and Nicobar Islands, India, HUMAN BIOL, 73(5), 2001, pp. 739-744

Authors: Pawar, AR Lu, CY Besmond, C Gorakshakar, AC Colah, RB Mohanty, D Krishnamoorthy, R

Citation: Ar. Pawar et al., A simple approach to the characterization of three common Indian beta-thalassemia mutations by artificially created restriction sites, HEMOGLOBIN, 24(4), 2000, pp. 311-318

Authors: Gorakshakar, AC Ghosh, K Colah, RB Mohanty, D

Citation: Ac. Gorakshakar et al., beta-thalassemia gene flow from India to Mauritius, AM J HEMAT, 65(3), 2000, pp. 263-264

Authors: Gorakshakar, AC Pawar, AR Nadkarni, AH Lu, CY Mohanty, D Krishnamoorthy, R Besmond, C Colah, RB

Citation: Ac. Gorakshakar et al., Potential of denaturing gradient gel electrophoresis for scanning of beta-thalassemia mutations in India, AM J HEMAT, 61(2), 1999, pp. 120-125