Myelodysplastic syndromes with deletions of chromosome 11q lack cryptic MLL rearrangement and exhibit characteristic clinicopathologic features.
about
The genetics of myelodysplastic syndrome: from clonal haematopoiesis to secondary leukaemiaH2AX deficiency is associated with erythroid dysplasia and compromised haematopoietic stem cell functionMDS with deletions in the long arm of chromosome 11 are associated with a high frequency of SF3B1 mutations.An uncommon t(9;11)(p24;q22) with monoallelic loss of and genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia
P2860
Myelodysplastic syndromes with deletions of chromosome 11q lack cryptic MLL rearrangement and exhibit characteristic clinicopathologic features.
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Myelodysplastic syndromes with ...... ic clinicopathologic features.
@ast
Myelodysplastic syndromes with ...... ic clinicopathologic features.
@en
type
label
Myelodysplastic syndromes with ...... ic clinicopathologic features.
@ast
Myelodysplastic syndromes with ...... ic clinicopathologic features.
@en
prefLabel
Myelodysplastic syndromes with ...... ic clinicopathologic features.
@ast
Myelodysplastic syndromes with ...... ic clinicopathologic features.
@en
P2093
P1433
P1476
Myelodysplastic syndromes with ...... ic clinicopathologic features.
@en
P2093
L Jeffrey Medeiros
Liping Zhang
Lynne V Abruzzo
Naomi Galili
Robert P Hasserjian
Yanpeng Zhang
P304
P356
10.1016/J.LEUKRES.2010.07.018
P577
2010-08-05T00:00:00Z