APA

Chapla A., Jayandharan G. R., Sumitha E., Sankari Devi G., Shenbagapriya P., Nair S. C., Viswabandya A., George B., Mathews V. & Srivastava A. (20111027). Molecular basis of hereditary factor V deficiency in India: identification of four novel mutations and their genotype-phenotype correlation. : Thrombosis and haemostasis.

Chicago

Chapla A, Jayandharan G R, Sumitha E, Sankari Devi G, Shenbagapriya P, Nair S C, Viswabandya A, George B, Mathews V and Srivastava A. 20111027. Molecular basis of hereditary factor V deficiency in India: identification of four novel mutations and their genotype-phenotype correlation. : Thrombosis and haemostasis.

Harvard

Chapla A., Jayandharan G. R., Sumitha E., Sankari Devi G., Shenbagapriya P., Nair S. C., Viswabandya A., George B., Mathews V. and Srivastava A. (20111027). Molecular basis of hereditary factor V deficiency in India: identification of four novel mutations and their genotype-phenotype correlation. : Thrombosis and haemostasis.

MLA

Chapla A, Jayandharan G R, Sumitha E, Sankari Devi G, Shenbagapriya P, Nair S C, Viswabandya A, George B, Mathews V and Srivastava A. Molecular basis of hereditary factor V deficiency in India: identification of four novel mutations and their genotype-phenotype correlation. : Thrombosis and haemostasis. 20111027.