机译:组合阵列CGH加SNP基因组在单一测定中分析,以优化临床测试
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Allina Cytogenetics Laboratory Abbott Northwestern Hospital Minneapolis MN United States;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Institute of Computer Science Warsaw University of Technology Warsaw Poland;
Department of Molecular and Medical Genetics Oregon Health and Sciences University-OHSU Portland;
Department of Pediatrics University of Mississippi Medical Center Jackson MS United States;
Department of Genetics University of Alabama Birmingham AL United States;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
Department of Molecular and Human Genetics Baylor College of Medicine One Baylor Plaza Houston;
absence of heterozygosity; array CGH; medically actionable variants; SNP; uniparental disomy;
机译:结合阵列CGH和SNP基因组分析在单个测定中进行优化的临床测试
机译:使用组合CGH-SNP阵列进行全基因组增生异常综合征中拷贝数变化和UPD基因组分析的意义。
机译:全基因组阵列CGH作为5080产前和产后病例的一线检测的临床实施
机译:遗传算法的应用 - 基于SIB对基因组SNP型谱的临床表型预测
机译:分析阵列CGH数据和当前状态数据。
机译:结合阵列CGH和SNP基因组分析在单个测定中进行优化的临床测试
机译:全基因组阵列CGH作为5080产前和产后病例的一线检测的临床实施