Familial risks for childhood acute lymphocytic leukaemia in Sweden and Finland: far exceeding the effects of known germline variants.
about
The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2AGermline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study.Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genesA genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia.
P2860
Familial risks for childhood acute lymphocytic leukaemia in Sweden and Finland: far exceeding the effects of known germline variants.
description
2012 nî lūn-bûn
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2012年の論文
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2012年論文
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2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
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2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
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2012年论文
@zh-cn
name
Familial risks for childhood a ...... ts of known germline variants.
@en
Familial risks for childhood a ...... ts of known germline variants.
@nl
type
label
Familial risks for childhood a ...... ts of known germline variants.
@en
Familial risks for childhood a ...... ts of known germline variants.
@nl
prefLabel
Familial risks for childhood a ...... ts of known germline variants.
@en
Familial risks for childhood a ...... ts of known germline variants.
@nl
P2860
P50
P921
P356
P1476
Familial risks for childhood a ...... ts of known germline variants.
@en
P2093
Elham Kharazmi
Miguel I da Silva Filho
P2860
P304
P356
10.1111/BJH.12069
P407
P577
2012-10-01T00:00:00Z