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Molecular basis of quantitative fibrinogen disorders in 27 patients from India.
Sumitha E, Jayandharan GR, Arora N, Abraham A, David S, Devi GS, Shenbagapriya P, Nair SC, George B, Mathews V, Chandy M, Viswabandya A, Srivastava A. Sumitha E, et al. Among authors: shenbagapriya p. Haemophilia. 2013 Jul;19(4):611-8. doi: 10.1111/hae.12143. Epub 2013 Apr 8. Haemophilia. 2013. PMID: 23560673
Molecular basis of hereditary factor V deficiency in India: identification of four novel mutations and their genotype-phenotype correlation.
Chapla A, Jayandharan GR, Sumitha E, Sankari Devi G, Shenbagapriya P, Nair SC, Viswabandya A, George B, Mathews V, Srivastava A. Chapla A, et al. Among authors: shenbagapriya p. Thromb Haemost. 2011 Jun;105(6):1120-3. doi: 10.1160/TH10-11-0767. Epub 2011 Apr 20. Thromb Haemost. 2011. PMID: 21647534 No abstract available.