domingo, 26 de julio de 2015

Genomics|Genetic Testing|Guidelines: Newborn Screening

Genomics|Genetic Testing|Guidelines

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Newborn Screening



GuidelineOrganizationPublished
Newborn screening and the role of the obstetrician-gynecologistExternal Web Site IconAmerican College of Obstetricians and GynecologistsExternal Web Site Icon2015
Whole-genome sequencing in newborn screeningExternal Web Site IconEuropean Society of Human Genetics,External Web Site Icon P3G International Paediatric Platform,External Web Site Icon Human Genome Organisation,External Web Site Icon PHG FoundationExternal Web Site Icon2015
Appropriateness of newborn screening for α1-antitrypsin deficiencyExternal Web Site IconAlpha-1 FoundationExternal Web Site Icon2014
Parental permission for pilot newborn screening researchExternal Web Site IconBioethics and Legal Work Group of the Newborn Screening Translational Research NetworkExternal Web Site Icon2014
Framework to start the debate on neonatal screening policies in the EUExternal Web Site IconExpert group2014
Newborn screening: education, consent, and the residual blood spotExternal Web Site IconNational Society of Genetic CounselorsExternal Web Site Icon2014
Including the initial newborn screening bloodspot collection device serial number on birth certificatesExternal Web Site IconSecretary of Health and Human Services Advisory Committee on Heritable Disorders in Newborns and ChildrenExternal Web Site Icon2013
Assessing and improving the methodological quality of economic evaluations of newborn screeningExternal Web Site IconExpert group2012

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