期刊
BRITISH JOURNAL OF HAEMATOLOGY
卷 111, 期 2, 页码 647-649出版社
BLACKWELL SCIENCE LTD
DOI: 10.1046/j.1365-2141.2000.02355.x
关键词
myeloproliferative disorder; translocation; FGFR1 gene; chromosome 8; chromosome 19
类别
Translocations affecting the chromosomal locus 8p12 are hallmarks of an atypical stem cell myeloproliferative disorder. These events disrupt the fibroblast growth factor receptor 1 (FGFR1) gene and fuse the FGFR1 C-terminus catalytic domain with unrelated proteins. Here, we report on the characterization of the 19q13.3 locus as the fifth FGFR1 chromosomal partner.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据