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WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features.
Am J Hum Genet. 2017 Jul 6;101(1):139-148. doi: 10.1016/j.ajhg.2017.06.002.
Am J Hum Genet. 2017.
PMID: 28686853
Free PMC article.
ABCB6 RNA expression in leukemias--expression is low in acute promyelocytic leukemia and FLT3-ITD-positive acute myeloid leukemia.
Abraham A, Karathedath S, Varatharajan S, Markose P, Chendamarai E, Jayavelu AK, George B, Srivastava A, Mathews V, Balasubramanian P.
Abraham A, et al. Among authors: markose p.
Ann Hematol. 2014 Mar;93(3):509-12. doi: 10.1007/s00277-013-1821-2. Epub 2013 Jun 22.
Ann Hematol. 2014.
PMID: 23793916
No abstract available.
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International reporting scale of BCR-ABL1 fusion transcript in chronic myeloid leukemia: first report from India.
Balasubramanian P, Chendamarai E, Markose P, Fletcher L, Branford S, George B, Mathews V, Chandy M, Srivastava A.
Balasubramanian P, et al. Among authors: markose p.
Acta Haematol. 2012;127(3):135-42. doi: 10.1159/000334716. Epub 2012 Jan 12.
Acta Haematol. 2012.
PMID: 22249155
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Spectrum of BCR-ABL kinase domain mutations in patients with chronic myeloid leukemia from India with suspected resistance to imatinib-mutations are rare and have different distributions.
Markose P, Chendamarai E, Balasubramanian P, Velayudhan SR, Srivastava VM, Mathews V, George B, Viswabandya A, Srivastava A, Chandy M.
Markose P, et al.
Leuk Lymphoma. 2009 Dec;50(12):2092-5. doi: 10.3109/10428190903332486.
Leuk Lymphoma. 2009.
PMID: 19925053
No abstract available.
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Corrections for self absorption in alpha souces.
Raghavayva M, Jha G, Markose PM.
Raghavayva M, et al. Among authors: markose pm.
Health Phys. 1975 Nov;29(5):782-5.
Health Phys. 1975.
PMID: 1193893
No abstract available.
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