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Genetic Variants for Long QT Syndrome among Infants and Children from a Statewide Newborn Hearing Screening Program Cohort

机译：从州所有新生儿听力筛查计划队列的婴儿和儿童长QT综合征的遗传变异

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Ruey-Kang R. Chang; Yueh-Tze Lan; Michael J. Silka; Hallie Morrow; Alan Kwong; Janna Smith-Lang; Robert Wallerstein; Henry J. Lin;
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1. Genetic variants for long QT syndrome among infants and children from a statewide newborn hearing screening program cohort [J] . ChangR.-K.R., LanY.-T., SilkaM.J., The Journal of pediatrics . 2014,第3期

机译：全州新生儿听力筛查计划队列中婴幼儿长QT综合征的遗传变异
2. The development of a genetic newborn screening assay for permanent hearing loss using blood spots - A collaboration between Newborn Screening Ontario (NSO) and the Infant Hearing Program (IHP) [J] . Yeh E., Durie D., McClelland S., Clinical Biochemistry . 2014,第15期

机译：使用血斑的永久性听力丧失的基因新生儿筛查测定方法的开发-安大略省新生儿筛查（NSO）与婴儿听力计划（IHP）的合作
3. Genetic characteristics of children and adolescents with long-QT syndrome diagnosed by school-based electrocardiographic screening programs. [J] . Masao Yoshinaga, Yu Kucho, Jav Sarantuya, Circulation. Arrhythmia and electrophysiology . 2014,第1期

机译：通过基于学校的心电图检查程序诊断出的具有长QT综合征的儿童和青少年的遗传特征。
4. The Johor Screening Scheme: Is an Area-Wide Newborn Hearing Screening Possible in Malaysia? [C] . Farah I. Corona-Strauss, Wolfgang Delb, Marc Bloching, International Conference on Intelligent Information Hiding and Multimedia Signal Processing . 2007

机译：柔佛州筛查计划：马来西亚是一个可能的新生儿听证筛查吗？
5. Universal newborn hearing screening: Program evaluation in a community-based hospital setting. [D] . Slider, Michele Louise. 2005

机译：新生儿通用听力筛查：在社区医院进行的计划评估。
6. Genetic variants for long QT syndrome among infants and children from a statewide newborn hearing screening program cohort [O] . Ruey-Kang R. Chang, Yueh-Tze Lan, Michael J. Silka, -1

机译：全州新生儿听力筛查计划队列中婴幼儿长QT综合征的遗传变异
7. Response to Letter Regarding Articles, “Prevalence of Long QT Syndrome Gene Variants in Sudden Infant Death Syndrome,” “Cardiac Sodium Channel Dysfunction in Sudden Infant Death Syndrome,” and “Contribution of Long-QT Syndrome Genes to Sudden Infant Death Syndrome: Is It Time to Consider Newborn Electrocardiographic Screening?” [O] . Peter J. Schwartz, Alfred L. George 2007

机译：回应关于文章的信，“长Qt综合征基因变异突发婴儿死亡综合征的患病率”，“突发性婴儿死亡综合征的心脏钠通道功能障碍”和“长QT综合征基因对突发婴儿死亡综合征的贡献：是是时候考虑新生儿心电图筛查？“
8. Sickle Cell Disease: Screening, Diagnosis, Management, and Counseling in Newborns and Infants. Clinical Practice Guideline Number 6; Sickle Cell Disease: Comprehensive Screening and Management in Newborns and Infants. Quick Reference Guide for Clinicians Number 6; Sickle Cell Disease in Newborns and Infants. A Guide for Parents [R] . 1993

机译：镰状细胞病：新生儿和婴儿的筛查，诊断，管理和咨询。临床实践指南第6号;镰状细胞病：新生儿和婴儿的综合筛查和管理。第6号临床医生快速参考指南;新生儿和婴儿的镰状细胞病。家长指南

Genetic Variants for Long QT Syndrome among Infants and Children from a Statewide Newborn Hearing Screening Program Cohort

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