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Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial

机译：评估北卡罗来纳州近期外科群体早期外壳测序的临床效用临床基因组评估下一代exome测序（NCGENES）2研究：随机对照试验

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Brooke S. Staley; Laura V. Milko; Margaret Waltz; Ida Griesemer; Lonna Mollison; Tracey L. Grant; Laura Farnan; Myra Roche; Angelo Navas; Alexandra Lightfoot; Ann Katherine M. Foreman; Julianne M. O’Daniel; Suzanne C. O’Neill; Feng-Chang Lin; Tamara S. Roman; Alicia Brandt; Bradford C. Powell; Christine Rini; Jonathan S. Berg; Jeannette T. Bensen;
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1. Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial [J] . Brooke S. Staley, Laura V. Milko, Margaret Waltz, Trials . 2021,第1期

机译：评估北卡罗来纳州北卡罗来纳州临床基因组评估下一代exome测序（NCGENES）2研究的临床纯粹肠道序列的临床效用2研究：随机对照试验
2. Evaluating parents’ decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol [J] . Laura V. Milko, Christine Rini, Megan A. Lewis, Trials . 2018,第1期

机译：在NC Nexus（北卡罗来纳州新生儿exame exorments excormence测序）中，评估父母对其孩子的下一代测序的决定（用于通用筛查）研究：随机对照试验方案
3. Challenges in detecting genomic copy number aberrations using next-generation sequencing data and the eXome Hidden Markov Model: a clinical exome-first diagnostic approach [J] . Toshiyuki Yamamoto, Keiko Shimojima, Yumiko Ondo, Human genome variation. . 2016,第1期

机译：使用下一代测序数据和eXome隐马尔可夫模型检测基因组拷贝数异常的挑战：临床外显子优先的诊断方法
4. Establish Reporting Format of Gene Related Rare-Diseases by Exome Sequencing in the Clinical Medical Laboratory [C] . Cheng-Mao Ho, Hsi-Yuan Huang, Chin-An Yang, IEEE International Conference on Bioinformatics and Bioengineering . 2016

机译：在临床医学实验室中通过外显子组测序建立与基因有关的罕见病报告格式
5. A Randomized, Double-blind, Placebo-controlled Clinical Trial Evaluating the Effect of Infliximab on General Cognition in a Population of Depressed Individuals with Bipolar Disorder Type I/II [D] . Pan, Zihang. 2018

机译：一项随机，双盲，安慰剂对照的临床试验，评估英夫利昔单抗对I / II型双相情感障碍抑郁症患者总体认知的影响
6. Evaluating parents’ decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol [O] . Laura V. Milko, Christine Rini, Megan A. Lewis, 2018

机译：在NC NEXUS（北卡罗来纳州新生儿外显子组测序通用筛查）研究中评估父母对孩子进行下一代测序的决定：一项随机对照试验方案
7. Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies [O] . F Mone, DJ McMullan, D Williams, 2021

机译：证据支持产前exome测序在评价胎儿的临床用途，先天性异常

Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial

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