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Molecular basis of Bernard-Soulier syndrome in 27 patients from India.
Sumitha E, Jayandharan GR, David S, Jacob RR, Sankari Devi G, Bargavi B, Shenbagapriya S, Nair SC, Abraham A, George B, Viswabandya A, Mathews V, Chandy M, Srivastava A. Sumitha E, et al. Among authors: jayandharan gr. J Thromb Haemost. 2011 Aug;9(8):1590-8. doi: 10.1111/j.1538-7836.2011.04417.x. J Thromb Haemost. 2011. PMID: 21699652 Free article.
Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin.
Jayandharan G, Viswabandya A, Baidya S, Nair SC, Shaji RV, George B, Chandy M, Srivastava A. Jayandharan G, et al. J Thromb Haemost. 2005 Jul;3(7):1482-7. doi: 10.1111/j.1538-7836.2005.01339.x. Epub 2005 May 9. J Thromb Haemost. 2005. PMID: 15892863 Free article.
Polymorphism in factor VII gene modifies phenotype of severe haemophilia.
Jayandharan GR, Nair SC, Poonnoose PM, Thomas R, John J, Keshav SK, Cherian RS, Devadarishini M, Lakshmi KM, Shaji RV, Viswabandya A, George B, Mathews V, Chandy M, Srivastava A. Jayandharan GR, et al. Haemophilia. 2009 Nov;15(6):1228-36. doi: 10.1111/j.1365-2516.2009.02080.x. Epub 2009 Aug 16. Haemophilia. 2009. PMID: 19686262
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: jayandharan gr. 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.
88 results