Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Search research articles

Related Experiment Videos

Genetic screening and the pediatrician

Pediatric Annals

|May 29, 2000

Summary

No abstract available in PubMed .

Related Experiment Videos

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by

Same author

Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card.

Pediatrics·2001

Same author

New England Consortium: a model for medical evaluation of expanded newborn screening with tandem mass spectrometry.

Journal of inherited metabolic disease·2001

Same author

Universal screening for congenital hearing loss.

Pediatric annals·2000

Same author

Glucose transporter type 1 deficiency: a study of two cases with video-EEG.

European journal of pediatrics·1999

Same author

Development of guidelines for treatment of children with phenylketonuria: report of a meeting at the National Institute of Child Health and Human Development held August 15, 1995, National Institutes of Health, Bethesda, Maryland.

Pediatrics·1999

Same author

Management of phenylketonuria for optimal outcome: a review of guidelines for phenylketonuria management and a report of surveys of parents, patients, and clinic directors.

Pediatrics·1999