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GENE-30. PRELIMINARY STUDY ON WHOLE-EXOME SEQUENCING TECHNOLOGY IN THE GENETIC ANALYSIS OF PEDIATRIC PATIENTS WITH GLIOMAS

机译：基因-30。脊髓灰质炎患者遗传分析全外膜测序技术的初步研究

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摘要

To analyze the genes related to the signaling pathways in pediatric gliomas and drug-related genes with whole-exome sequencing technology.

机译：分析与全全外测序技术的小儿胶质瘤和药物相关基因中的信号通路相关的基因。

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期刊名称 Neuro-Oncology
作者
Mingyao Lai; Juan Li; Junjie Zhen; jiangfen zhou; Qingjun Hu; Minting ye; Shaoqun Li; Lichao Wang; Cheng Zhou; Zhaoming Zhou; Linbo Cai;
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年(卷),期 2019(21),Suppl 6
年度 2019
页码 vi104
总页数 1
原文格式 PDF
正文语种
中图分类神经病学;肿瘤学;
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专利

1. Is Whole-Exome Sequencing an Ethically Disruptive Technology? Perspectives of Pediatric Oncologists and Parents of Pediatric Patients With Solid Tumors [J] . McCullough Laurence B., Slashinski Melody J., McGuire Amy L., Pediatric blood & cancer . 2016,第3期

机译：全外显子测序是否符合道德规范？小儿肿瘤科医生和小儿实体瘤患者父母的观点
2. Whole-Exome Sequencing Reveals Novel Genetic Variation for Dilated Cardiomyopathy in Pediatric Chinese Patients [J] . Dai Genyin, Pu Zhening, Cheng Xueying, Pediatric cardiology . 2019,第5期

机译：全拓序列揭示了小儿患者扩张心肌病的新型遗传变异
3. Success of Face Analysis Technology in Rare Genetic Diseases Diagnosed by Whole-Exome Sequencing: A Single-Center Experience [J] . Muhsin Elmas, Basak Gogus Molecular syndromology . 2020,第1期

机译：全外壳测序诊断稀有遗传疾病中面分析技术的成功：单中心体验
4. Homozygosity Mapping using Whole-Exome Sequencing: A Valuable Approach for Pathogenic Variant Identification in Genetic Diseases [C] . Jorge Oliveira, Rute Pereira, Rosario Santos, International Conference on Bioinformatics Models, Methods and Algorithms . 2017

机译：纯合子映射使用全exome测序：一种有价值的遗传疾病致病变异鉴定的方法
5. Discovery of novel genes that cause rare pediatric renal diseases using whole-exome sequencing [D] . Lemaire, Mathieu. 2015

机译：使用全基因组测序发现导致罕见的小儿肾脏疾病的新基因
6. Success of Face Analysis Technology in Rare Genetic Diseases Diagnosed by Whole-Exome Sequencing: A Single-Center Experience [O] . Muhsin Elmas, Basak Gogus 2020

机译：全拓序测序诊断稀有遗传疾病中面分析技术的成功：单中心经验
7. Success of Face Analysis Technology in Rare Genetic Diseases Diagnosed by Whole-Exome Sequencing: A Single-Center Experience [O] . Muhsin Elmas, Basak Gogus 2020

机译：全拓序测序诊断稀有遗传疾病中面分析技术的成功：单中心经验

GENE-30. PRELIMINARY STUDY ON WHOLE-EXOME SEQUENCING TECHNOLOGY IN THE GENETIC ANALYSIS OF PEDIATRIC PATIENTS WITH GLIOMAS

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