A new recurring chromosome 13 abnormality in two older patients with de novo acute myeloid leukemia: An Indian experience.
dc.contributor.author | Trivedi, P J | |
dc.contributor.author | Patel, P S | |
dc.contributor.author | Brahmbhatt, M M | |
dc.contributor.author | Patel, B P | |
dc.contributor.author | Gajjar, S B | |
dc.contributor.author | Dalal, E N | |
dc.contributor.author | Shukla, S N | |
dc.contributor.author | Shah, P M | |
dc.contributor.author | Bakshi, S R | |
dc.date.accessioned | 2012-06-08T06:40:54Z | |
dc.date.available | 2012-06-08T06:40:54Z | |
dc.date.issued | 2009-09 | |
dc.description.abstract | We report here two cases of trisomy 13 in acute myeloid leukemia M1 subtype. short-term unstimulated bone marrow and peripheral blood lymphocyte culture showed 47, XY, +13 in all metaphase plates and trisomy 13 was confirmed with whole chromosome paint probes. Trisomy 13 in AML-M1 is a rare numerical abnormality. This is the first Indian report of sole trisomy 13 in AML-M1. Here, we present two cases of elder male patients, which may constitute a distinct subtype. | en_US |
dc.identifier.citation | Trivedi P J, Patel P S, Brahmbhatt M M, Patel B P, Gajjar S B, Dalal E N, Shukla S N, Shah P M, Bakshi S R. A new recurring chromosome 13 abnormality in two older patients with de novo acute myeloid leukemia: An Indian experience. Indian Journal of Human Genetics. 2009 Sept; 15(3): 137-139. | en_US |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/138886 | |
dc.language.iso | en | en_US |
dc.source.uri | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2922630/ | en_US |
dc.subject | Acute myeloid leukemia-M1 | en_US |
dc.subject | recurrent | en_US |
dc.subject | sole abnormality | en_US |
dc.subject | trisomy 13 | en_US |
dc.subject.mesh | Aged | |
dc.subject.mesh | Bone Marrow Cells --cytology | |
dc.subject.mesh | Cells, Cultures | |
dc.subject.mesh | Chromosome Aberrations --genetics | |
dc.subject.mesh | Chromosomes, Human, Pair 13 --genetics | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Lymphocytes --blood | |
dc.subject.mesh | Lymphocytes --cytology | |
dc.subject.mesh | India --epidemiology | |
dc.subject.mesh | In Situ Hybridization, Fluorescence --methods | |
dc.subject.mesh | Leukemia, Myeloid, Acute --diagnosis | |
dc.subject.mesh | Leukemia, Myeloid, Acute --genetics | |
dc.subject.mesh | Male | |
dc.subject.mesh | Trisomy --genetics | |
dc.title | A new recurring chromosome 13 abnormality in two older patients with de novo acute myeloid leukemia: An Indian experience. | en_US |
dc.type | Article | en_US |
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