Molecular inversion probes reveal patterns of 9p21 deletion and copy number aberrations in childhood leukemia.
第一作者:
Joshua D,Schiffman
第一单位:
Pediatric Hematology/Oncology and Oncological Sciences, Huntsman Cancer Institute, University of Utah, 2000 Circle of Hope, Room 4343, Salt Lake City, UT 84112. Joshua.Schiffman@hci.utah.edu
作者:
主题词
青少年(Adolescent);伯基特淋巴瘤(Burkitt Lymphoma);儿童(Child);儿童, 学龄前(Child, Preschool);染色体倒位(Chromosome Inversion);染色体, 人, 9对(Chromosomes, Human, Pair 9);细胞遗传学分析(Cytogenetic Analysis);数据说明, 统计(Data Interpretation, Statistical);女(雌)性(Female);基因缺失(Gene Deletion);基因剂量(Gene Dosage);基因, p16(Genes, p16);人类(Humans);原位杂交, 荧光(In Situ Hybridization, Fluorescence);婴儿(Infant);核型分析(Karyotyping);白血病, 髓系, 慢性, BCR-ABL阳性(Leukemia, Myelogenous, Chronic, BCR-ABL Positive);白血病, 髓样, 急性(Leukemia, Myeloid, Acute);男(雄)性(Male);分子探针技术(Molecular Probe Techniques);聚合酶链反应(Polymerase Chain Reaction);多态性, 单核苷酸(Polymorphism, Single Nucleotide);前体B细胞淋巴母细胞白血病淋巴瘤(Precursor B-Cell Lymphoblastic Leukemia-Lymphoma);前体T细胞淋巴母细胞白血病淋巴瘤(Precursor T-Cell Lymphoblastic Leukemia-Lymphoma);结果可重复性(Reproducibility of Results)
DOI
10.1016/j.cancergencyto.2009.03.005
PMID
19602459
发布时间
2021-10-20
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