Newborn screening compared to clinical identification of biochemical genetic disorders

Author:

Waisbren S. E.1,Read C. Y.2,Ampola M.3,Brewster T. G.4,Demmer L.5,Greenstein R.6,Ingham C. L.7,Korson M.3,Msall M.8,Pueschel S.8,Seashore M.9,Shih E.10,Levy H. L.1

Affiliation:

1. ; Children's Hospital; Boston Massachusetts

2. ; Boston College School of Nursing; Chestnut Hill Massachusetts

3. New; Boston Massachusetts England Medical Center

4. ; Maine Medical Center; Portland Maine

5. ; University of Massachusetts Medical Center; Worcester Massachusetts

6. ; Connecticut Children's Medical Center; Hartford Connecticut

7. ; Vermont Department of Health; Burlington Vermont

8. ; Rhode Island Hospital; Providence Rhode Island

9. ; Yale University School of Medicine; New Haven Connecticut

10. ; Massachusetts General Hospital; Boston Massachusetts USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference2 articles.

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3. Long-term outcome of expanded newborn screening at Boston children’s hospital: benefits and challenges in defining true disease;Journal of Inherited Metabolic Disease;2017-01-04

4. Newborn Metabolic Screening: Reference Diagnostic Method Evaluation;Sarem Journal of Reproductive Medicine;2016-10-01

5. Avaliação econômica em saúde: triagem neonatal da galactosemia;Cadernos de Saúde Pública;2011-04

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