Your browser doesn't support javascript.
loading
A case of acute myeloid leukemia-M2 with trisomy 4 in addition to t(8;21).
Indian J Hum Genet ; 2008 Jan; 14(1): 20-22
Artigo em Inglês | IMSEAR | ID: sea-138845
ABSTRACT
t(8;21)(q22;q22) is the most frequently observed karyotypic abnormality associated with acute myeloid leukemia (AML), specifically in FAB-M2. Short-term unstimulated bone marrow (BM) and peripheral blood lymphocyte culture showed 47,XX, +4,t(8;21) in all metaphase plates; and interphase and metaphase results of AML-ETO fusion was positive and trisomy of 4 was confirmed with WCP probes. Trisomy 4 in AML with t(8;21) is a rare numerical abnormality. Here we present such case of patient which may constitute a distinctive subtype.

Texto completo: DisponíveL Índice: IMSEAR (Sudeste Asiático) Idioma: Inglês Revista: Indian J Hum Genet Ano de publicação: 2008 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: IMSEAR (Sudeste Asiático) Idioma: Inglês Revista: Indian J Hum Genet Ano de publicação: 2008 Tipo de documento: Artigo