Search Results - Ashraf Mannan
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An insight on the role of genetic testing of RUNX1: A key transcriptional gene in familial platelet disorder with predisposition to acute myeloid leukemia by Intezar Mehdi, K. Ramya, T.L. Suma, Ashraf Mannan, M.L. Sheela, Shanmukh Kattragada, B.S. Ajaikumar, Mithua Ghosh
Published 2023Call Number: Loading…Connect to this object online.
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