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Long-term follow-up after diagnosis resulting from newborn screening: Statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children

机译：新生儿筛查诊断后的长期随访：美国卫生和人类服务咨询委员会关于新生儿和儿童遗传性疾病和遗传疾病咨询委员会的声明

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Alex R Kemper; Coleen A Boyle; Javier Aceves; Denise Dougherty; James Figge; Jill L Fisch; Alan R Hinman; Carol L Greene; Christopher A Kus; Julie Miller; Derek Robertson; Brad Therrell; Michele Lloyd-Puryear; Peter C van Dyck; R Rodney Howell;
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1. Long-term follow-up after diagnosis resulting from newborn screening: statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children. [J] . Kemper AR, Boyle CA, Aceves J, Genetics in medicine . 2008,第4期

机译：新生儿筛查诊断后的长期随访：美国卫生和公共服务大臣关于新生儿和儿童遗传性疾病和遗传疾病咨询委员会的声明。
2. What questions should newborn screening long-term follow-up be able to answer? A statement of the US Secretary for Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children. [J] . Hinton CF, Feuchtbaum L, Kus CA, Genetics in medicine . 2011,第10期

机译：新生儿筛查长期随访应该回答哪些问题？美国卫生与公共服务部长咨询委员会关于新生儿和儿童遗传性疾病的声明。
3. Including the initial newborn screening bloodspot collection device serial number on birth certificates: Basis and recommendations from the Secretary of Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children [J] . TherrellB.L., WuC. Genetics in medicine . 2013,第3期

机译：包括出生证明上的初始新生儿筛查血斑采集设备序列号：卫生和公共服务部长的新生儿和儿童遗传性疾病咨询委员会的依据和建议
4. Characterizing blood disease markers in neonates with cerebrotendinous xanthomatosis; a step toward newborn screening for this neurodegenerative bile acid disorder [C] . Andrea E DeBarber, Robert D Steiner American Society for Mass Spectrometry Conference on Mass Spectrometry and Allied Topics . 2012

机译：用脑血管瘤症表征新生儿的血液疾病标志物;新生儿筛查这种神经变性胆汁酸病症的一步
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. Concerns of Newborn Blood Screening Advisory Committee Members Regarding Storage and Use of Residual Newborn Screening Blood Spots [O] . Erin W. Rothwell, Rebecca A. Anderson, Matthew J. Burbank, 2011

机译：新生儿血液筛查咨询委员会成员有关残留和残留新生儿筛查血斑的存储和使用的担忧
7. Including the initial newborn screening bloodspot collection device serial number on birth certificates: basis and recommendations from the Secretary of Health and Human Services’ Advisory Committee on Heritable Disorders in Newborns and Children [O] . Bradford L. Therrell, Colleen Wu 2012

机译：包括初始新生儿筛查血迹收集设备序列号出生证明：卫生和人类服务秘书委员会和新生儿遗传性疾病咨询委员会的基础和建议
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

Long-term follow-up after diagnosis resulting from newborn screening: Statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children

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