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Policy brief: Improve coverage of newborn genetic screening to include the Recommended Uniform Screening Panel and newborn screening registry

机译：政策简介：提高新生儿遗传筛查的覆盖范围包括推荐的均匀筛选面板和新生儿筛选登记处

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Angela Starkweather; Bernice Coleman; Veronica Barcelona de Mendoza; Mei Fu; Jacquelyn Taylor; Wendy Henderson; Carole Kenner; Deborah Walker; Linda Amankwaa; Cindy Anderson;
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1. Policy brief: Improve coverage of newborn genetic screening to include the Recommended Uniform Screening Panel and newborn screening registry [J] . Starkweather Angela, Coleman Bernice, de Mendoza Veronica Barcelona, Nursing outlook . 2017,第4期

机译：政策简介：提高新生儿遗传筛查的覆盖范围包括推荐的均匀筛选面板和新生儿筛查登记处
2. The AJMG SEQUENCE: Decoding news and trends for the medical genetics communitySCID suggested for uniform newborn screening panel. [J] . Levenson D American journal of medical genetics, Part A . 2010,第6期

机译：AJMG序列：为医学遗传学界解码新闻和趋势SCID建议用于统一新生儿筛查小组。
3. High incidence of maternal vitamin B12 deficiency detected by newborn screening: first results from a study for the evaluation of 26 additional target disorders for the German newborn screening panel [J] . Gwendolyn Gramer1, Junmin Fang-Hoffmann1, Patrik Feyh1, 世界儿科杂志(英文版) . 2018,第005期

机译：新生儿筛查发现孕妇维生素B12缺乏症的高发：德国新生儿筛查小组评估26种其他目标疾病的研究的第一项结果
4. Improving analysis and reporting for Virginia's Division of Consolidated Laboratory Services newborn screening program [C] . Chris Patrick, Hampton Leonard, Wendy Novicoff, Systems and Information Engineering Design Symposium . 2017

机译：改善弗吉尼亚州综合实验室服务部门新生儿筛查计划的分析和报告
5. The role of the genetic counselor in newborn screening follow-up services: Recommendations regarding genetic counselor roles and education in anticipation of increased population-based screening. [D] . Giordano, Jessica L. 2008

机译：遗传咨询师在新生儿筛查随访服务中的作用：关于遗传咨询师在预期以人群为基础的筛查方面的作用和教育的建议。
6. Policy brief: Improve coverage of newborn genetic screening to include the Recommended Uniform Screening Panel and newborn screening registry [O] . Angela Starkweather, Bernice Coleman, Veronica Barcelona de Mendoza, -1

机译：政策简介：扩大新生儿基因筛查的覆盖范围以包括推荐的统一筛查小组和新生儿筛查注册表
7. Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretaryu27s Advisory Committee on Heritable Disorders in Newborns and Children [O] . Kemper Alex R., Green Nancy S., Calonge Ned, 2014

机译：针对推荐的统一筛查小组提名的条件的决策过程：美国卫生和公共服务部秘书处关于新生儿和儿童遗传性疾病咨询委员会的声明
8. Newborn Screening for Cystic Fibrosis: A Paradigm for Public Health Genetics211 Policy Development. Proceedings of a Workshop. Held in Atlanta, Georgia in 211 January 1997. Morbidity and Mortality Weekly Report, Vol. 46, No. RR-16, December 211 12, 1997 [R] . Cono, J., Qualls, N. L., Khoury, M. J., 1997

机译：新生儿囊性纤维化筛查：公共卫生遗传学的一种范例211政策制定。研讨会的会议记录。 1997年1月21日在佐治亚州亚特兰大市举行。发病率和死亡率周报，第一卷。 46，编号RR-16，1997年12月211日12

Policy brief: Improve coverage of newborn genetic screening to include the Recommended Uniform Screening Panel and newborn screening registry

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