Items where Author is "nair, S. C."
Group by: Item Type | No Grouping Number of items: 1. Jayandharan, G. ; Viswabandya, A. ; Baidya, S. ; nair, S. C. ; shaji, R. V. ; George, B. ; Chandy, M. ; Srivastava, A. (2005) 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 Journal of Thrombosis and Haemostasis, 3 (7). pp. 1482-1487. ISSN 1538-7933 |
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