An insight on the role of genetic testing of RUNX1: A key transcriptional gene in familial platelet disorder with predisposition to acute myeloid leukemia door Intezar Mehdi, K. Ramya, T.L. Suma, Ashraf Mannan, M.L. Sheela, Shanmukh Kattragada, B.S. Ajaikumar, Mithua Ghosh

Volledige tekst