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Implementing comprehensive genetic carrier screening in China―Harnessing the power of genomic medicine for the effective prevention/management of birth defects and rare genetic diseases in China 被引量:5
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作者 Yiping Shen Xiaoxia Qiu +6 位作者 Baohen Gui Sheng He Hefeng Huang jingjie xue Xiangming Xu xue Zhang Lin He 《Pediatric Investigation》 2018年第1期30-36,共7页
Carrier screening had been demonstrated as a powerful practice in preventing selected severe genetic disorders. This practice is expanding its scope and impact in the era of next-generation sequencing. Empirical and t... Carrier screening had been demonstrated as a powerful practice in preventing selected severe genetic disorders. This practice is expanding its scope and impact in the era of next-generation sequencing. Empirical and theoretical data support the utility of expanded carrier screening. The authors propose a comprehensive carrier screening program as a main component of the first-tier measure in preventing severe genetic disorders and birth defects in China. We discussed the key principles and important aspects to ensure the success of such a program. The authors believe this program will play a pivotal role in our endeavor for a healthier nation. 展开更多
关键词 CARRIER screening Next generation SEQUENCING BIRTH defect GENETIC disease
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