Loci other than 21q22.12 (RUNX1) and 16q21-23.2 cause familial AML.

Sellick, G S; Pritchard-Jones, K; Shepherd, V; Swansbury, J; Catovsky, D; Houlston, R S

Sellick, G S; Pritchard-Jones, K; Shepherd, V; Swansbury, J; Catovsky, D; Houlston, R S.

Leukemia ; 19(3): 465-6, 2005 Mar.

Article in En | MEDLINE | ID: mdl-15674419

Subject(s)

Chromosomes, Human, Pair 16/genetics; Chromosomes, Human, Pair 21/genetics; DNA-Binding Proteins/genetics; Leukemia, Myeloid, Acute/genetics; Proto-Oncogene Proteins/genetics; Transcription Factors/genetics; Core Binding Factor Alpha 2 Subunit; Family Health; Humans; Leukemia, Myeloid, Acute/etiology; Pedigree

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Database: MEDLINE Main subject: Transcription Factors / Chromosomes, Human, Pair 16 / Chromosomes, Human, Pair 21 / Leukemia, Myeloid, Acute / Proto-Oncogene Proteins / DNA-Binding Proteins Type of study: Etiology_studies Limits: Humans Language: En Year: 2005 Type: Article

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