Literature DB >> 1897259

Introduction: new technologies for genetic and newborn screening.

M R Seashore1, C Walsh-Vockley.   

Abstract

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.

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Mesh:

Year:  1991        PMID: 1897259      PMCID: PMC2589455     

Source DB:  PubMed          Journal:  Yale J Biol Med        ISSN: 0044-0086


  4 in total

Review 1.  Diagnosis of human immunodeficiency virus infection in infants and children.

Authors:  R N Husson; A M Comeau; R Hoff
Journal:  Pediatrics       Date:  1990-07       Impact factor: 7.124

2.  American Academy of Pediatrics Committee on Genetics: Newborn screening fact sheets.

Authors: 
Journal:  Pediatrics       Date:  1989-03       Impact factor: 7.124

3.  Tay-sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay.

Authors:  J S O'Brien; S Okada; A Chen; D L Fillerup
Journal:  N Engl J Med       Date:  1970-07-02       Impact factor: 91.245

4.  Genetic screening: marvel or menace?

Authors:  P T Rowley
Journal:  Science       Date:  1984-07-13       Impact factor: 47.728

  4 in total
  1 in total

1.  Demographic Studies from a National Gaucher Disease Screening Program.

Authors:  D M Gagnon; E Pergament; B A Fine
Journal:  J Genet Couns       Date:  1998-10       Impact factor: 2.537

  1 in total

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