Single nucleotide polymorphism microarray analysis of karyotypically normal acute myeloid leukemia reveals frequent copy number neutral loss of heterozygosity | Haematologica

Anne Tyyb?kinoja; Erkki Elonen; Hanna Vauhkonen; Janna Saarela; Sakari Knuutila

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Single nucleotide polymorphism microarray analysis of karyotypically normal acute myeloid leukemia reveals frequent copy number neutral loss of heterozygosity | Haematologica

机译：核型正常急性髓细胞白血病的单核苷酸多态性微阵列分析显示频繁拷贝数中性杂合性丧失血液学

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来源
《Haematologica》 |2008年第4期|共2页
作者
Anne Tyyb?kinoja; Erkki Elonen; Hanna Vauhkonen; Janna Saarela; Sakari Knuutila;
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中图分类血液及淋巴系疾病;
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1. Clinical Significance of Previously Cryptic Copy Number Alterations and Loss of Heterozygosity in Pediatric Acute Myeloid Leukemia and Myelodysplastic Syndrome Determined Using Combined Array Comparative Genomic Hybridization plus Single-Nucleotide Polymorphism Microarray Analyses [J] . Kyung-Nam Koh, Jin Ok Lee, Eul Ju Seo, Journal of Korean medical science . 2014,第7期

机译：应用组合阵列比较基因组杂交和单核苷酸多态性微阵列分析确定小儿急性髓样白血病和骨髓增生异常综合征中以前的密码拷贝数改变和杂合性丧失的临床意义
2. Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes. [J] . Barresi V, Romano A, Musso N, Genes, Chromosomes and Cancer . 2010,第11期

机译：正常核型急性髓细胞白血病基因组中杂合子区域的广泛拷贝中性丢失和罕见的重复出现的拷贝数异常。
3. Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis [J] . L Bullinger, J Kr?nke, C Sch?n, Leukemia . 2010,第2期

机译：使用高分辨率单核苷酸多态性分析鉴定细胞遗传学正常急性髓细胞性白血病中获得性拷贝数改变和单亲双体性
4. Cancer Classification Using Loss of Heterozygosity Data Derived from Single-Nucleotide Polymorphism Genotyping Arrays [C] . Wang, Yuhang Engineering in Medicine and Biology Society, 2006 Annual International Conference of the IEEE . 2006

机译：使用来自单核苷酸多态性基因分型阵列的杂合性数据丢失进行癌症分类
5. Clinical Significance of Previously Cryptic Copy Number Alterations and Loss of Heterozygosity in Pediatric Acute Myeloid Leukemia and Myelodysplastic Syndrome Determined Using Combined Array Comparative Genomic Hybridization plus Single-Nucleotide Polymorphism Microarray Analyses [O] . Kyung-Nam Koh, Jin Ok Lee, Eul Ju Seo, 2014

机译：组合阵列比较基因组杂交加单核苷酸多态性微阵列分析确定小儿急性髓细胞性白血病和骨髓增生异常综合症以前的阴行拷贝数改变和杂合性丧失的临床意义
6. Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group [O] . Xinjie Xu, Christine Bryke, Madina Sukhanova, 2018

机译：在基因组中评估拷贝数异常和复制中性杂合性作为急性髓性白血病诊断评估的最佳实践：从癌症基因组学结盟（CGC）骨髓肿瘤工作组的基于循证审查

Single nucleotide polymorphism microarray analysis of karyotypically normal acute myeloid leukemia reveals frequent copy number neutral loss of heterozygosity | Haematologica

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