Detection of cryptic chromosomal lesions including acquired segmental uniparental disomy in advanced and low-risk myelodysplastic syndromes.
作者:
主题词
成年人(Adult);老年人(Aged);老年人, 80以上(Aged, 80 and over);病例对照研究(Case-Control Studies);染色体畸变(Chromosome Aberrations);基因剂量(Gene Dosage);人类(Humans);核型分析(Karyotyping);杂合子丢失(Loss of Heterozygosity);中年人(Middle Aged);骨髓增生异常综合征(Myelodysplastic Syndromes);寡核苷酸序列分析(Oligonucleotide Array Sequence Analysis);多态性, 单核苷酸(Polymorphism, Single Nucleotide);单亲二体性(Uniparental Disomy)
DOI
10.1016/j.exphem.2007.08.009
PMID
17920760
发布时间
2007-11-02
- 浏览13

Experimental hematology
1728-38页
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文