Publications by authors named "R Angalena"

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Compound heterozygote condition in beta thalassemia major due to a novel single nucleotide deletion (-T) at codon 69 in association with IVS 1-5 (G>C) mutation.
R Angalena, S Aggarwal, S R Phadke, A Dalal

Int J Lab Hematol· August 2012

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A novel homozygous point mutation at codon 82 (HBB:c.247A > T) in the beta-globin gene leads to thalassemia major.
R Angalena, K N Prabitha, A K Chaudhary, M D Bashyam, S Jain

Int J Lab Hematol· October 2010

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Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South Indians.
Sm Naushad, Nurul Jain Jamal, R Angalena, C Krishna Prasad, A Radha Rama Devi

Blood Coagul Fibrinolysis· March 2007

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Familial (9;11)(p22;p15.5)pat translocation and XX sex reversal in a phenotypic boy with cryptorchidism and delayed development.
K Prabhakara, R Angalena, A Radha Ramadevi

Genet Couns· July 2004

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