Zobrazeno 1 - 2
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pro vyhledávání: '"Subhajit Bramha"'
Autor:
Ravikiran N Pawar, Sambhunath Banerjee, Subhajit Bramha, Shekhar Krishnan, Arpita Bhattacharya, Vaskar Saha, Anupam Chakrapani, Saurabh Bhave, Mammen Chandy, Reena Nair, Mayur Parihar, Neeraj Arora, D K Mishra
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 60, Iss 1, Pp 43-49 (2017)
Introduction: Mixed-phenotype acute leukemias (MPALs) are a heterogeneous group of rare leukemias constituting approximately 2%–5% of all leukemias, in which assigning a single lineage of origin is not possible. They are diagnosed by either the pre
Externí odkaz:
https://doaj.org/article/cd11d9912752401cb44cacf06ed96f1c
Autor:
Pawar, Ravikiran N., Sambhunath Banerjee, Subhajit Bramha, Shekhar Krishnan, Arpita Bhattacharya, Vaskar Saha, Anupam Chakrapani, Saurabh Bhave, Mammen Chandy, Reena Nair, Mayur Parihar, Neeraj Arora, Mishra, D. K.
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 60, Iss 1, Pp 43-49 (2017)
Pawar, R N, Banerjee, S, Bramha, S, Krishnan, S, Bhattacharya, A, Saha, V, Chakrapani, A, Bhave, S, Chandy, M, Nair, R, Parihar, M, Arora, N & Mishra, D K 2017, ' Mixed-phenotypic acute leukemia series from tertiary care center ', Indian journal of pathology & microbiology, vol. 60, no. 1, pp. 43-49 . < http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2017;volume=60;issue=1;spage=43;epage=49;aulast=Pawar >
University of Manchester-PURE
Pawar, R N, Banerjee, S, Bramha, S, Krishnan, S, Bhattacharya, A, Saha, V, Chakrapani, A, Bhave, S, Chandy, M, Nair, R, Parihar, M, Arora, N & Mishra, D K 2017, ' Mixed-phenotypic acute leukemia series from tertiary care center ', Indian journal of pathology & microbiology, vol. 60, no. 1, pp. 43-49 . < http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2017;volume=60;issue=1;spage=43;epage=49;aulast=Pawar >
University of Manchester-PURE
INTRODUCTION: Mixed-phenotype acute leukemias (MPALs) are a heterogeneous group of rare leukemias constituting approximately 2%-5% of all leukemias, in which assigning a single lineage of origin is not possible. They are diagnosed by either the prese