换一批
换一批250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies.
作者：
主题词
青少年(Adolescent);成年人(Adult);老年人(Aged);人类(Humans);核型分析(Karyotyping);中年人(Middle Aged);突变(Mutation);突变, 误义(Mutation, Missense);骨髓增生异常-骨髓增殖性疾病(Myelodysplastic-Myeloproliferative Diseases);点突变(Point Mutation);多态性, 单核苷酸(Polymorphism, Single Nucleotide);原癌基因蛋白质c-cbl(Proto-Oncogene Proteins c-cbl);单亲二体性(Uniparental Disomy);青年人(Young Adult)
DOI
10.1158/0008-5472.CAN-08-2754
PMID
19074904
发布时间
2021-12-03
- 浏览17
Cancer research
10349-57页
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