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Introduction: new technologies for genetic and newborn screening.
Screening newborn infants for inherited disorders has been effective in preventing mental retardation, growth failure, and death from several metabolic disorders for more than two decades. Technical advances have provided more screening tools for both genetic and nongenetic conditions, and in the co...
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Yale Journal of Biology and Medicine
1991
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2589455/ https://www.ncbi.nlm.nih.gov/pubmed/1897259 |
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author | Seashore, M. R. Walsh-Vockley, C. |
author_facet | Seashore, M. R. Walsh-Vockley, C. |
author_sort | Seashore, M. R. |
collection | PubMed |
description | Screening newborn infants for inherited disorders has been effective in preventing mental retardation, growth failure, and death from several metabolic disorders for more than two decades. Technical advances have provided more screening tools for both genetic and nongenetic conditions, and in the coming decades these techniques will be used not only to screen newborns but to assess genetic risks in entire populations. The financial, legal, and ethical issues which these activities raise must influence the development of public policies in order to reap the benefits promised. The conference published here was designed to address these issues for health care practitioners, health policy planners, and public health professionals. |
format | Text |
id | pubmed-2589455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | Yale Journal of Biology and Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-25894552008-11-28 Introduction: new technologies for genetic and newborn screening. Seashore, M. R. Walsh-Vockley, C. Yale J Biol Med Research Article Screening newborn infants for inherited disorders has been effective in preventing mental retardation, growth failure, and death from several metabolic disorders for more than two decades. Technical advances have provided more screening tools for both genetic and nongenetic conditions, and in the coming decades these techniques will be used not only to screen newborns but to assess genetic risks in entire populations. The financial, legal, and ethical issues which these activities raise must influence the development of public policies in order to reap the benefits promised. The conference published here was designed to address these issues for health care practitioners, health policy planners, and public health professionals. Yale Journal of Biology and Medicine 1991 /pmc/articles/PMC2589455/ /pubmed/1897259 Text en |
spellingShingle | Research Article Seashore, M. R. Walsh-Vockley, C. Introduction: new technologies for genetic and newborn screening. |
title | Introduction: new technologies for genetic and newborn screening. |
title_full | Introduction: new technologies for genetic and newborn screening. |
title_fullStr | Introduction: new technologies for genetic and newborn screening. |
title_full_unstemmed | Introduction: new technologies for genetic and newborn screening. |
title_short | Introduction: new technologies for genetic and newborn screening. |
title_sort | introduction: new technologies for genetic and newborn screening. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2589455/ https://www.ncbi.nlm.nih.gov/pubmed/1897259 |
work_keys_str_mv | AT seashoremr introductionnewtechnologiesforgeneticandnewbornscreening AT walshvockleyc introductionnewtechnologiesforgeneticandnewbornscreening |