A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.
第一作者:
J,Vijayakrishnan
第一单位:
Division of Genetics and Epidemiology, The Institute of Cancer Research, Sutton, UK.
作者:
医学主题词
病例对照研究(Case-Control Studies);儿童(Child);儿童, 学龄前(Child, Preschool);染色质组装和分解(Chromatin Assembly and Disassembly);染色体缺失(Chromosome Deletion);染色体, 人, 10对(Chromosomes, Human, Pair 10);染色体, 人, 12对(Chromosomes, Human, Pair 12);计算生物学(Computational Biology);女(雌)性(Female);基因表达谱(Gene Expression Profiling);基因座(Genetic Loci);疾病遗传易感性(Genetic Predisposition to Disease);全基因组关联研究(Genome-Wide Association Study);基因型(Genotype);高通量核苷酸序列分析(High-Throughput Nucleotide Sequencing);人类(Humans);婴儿(Infant);男(雄)性(Male);分子序列注释(Molecular Sequence Annotation);多态性, 单核苷酸(Polymorphism, Single Nucleotide);前体细胞淋巴母细胞白血病淋巴瘤(Precursor Cell Lymphoblastic Leukemia-Lymphoma);数量性状基因座位(Quantitative Trait Loci);序列分析, DNA(Sequence Analysis, DNA)
DOI
10.1038/leu.2016.271
PMID
27694927
发布时间
2025-05-30
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Leukemia
573-579页
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