Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project-Reference-Cited by-同舟云学术

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

Published:2020-10 Issue:4 Volume:107 Page:596-611
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Roman Tamara S.^ORCID,Crowley Stephanie B.,Roche Myra I.,Foreman Ann Katherine M.,O’Daniel Julianne M.,Seifert Bryce A.,Lee Kristy,Brandt Alicia,Gustafson Chelsea,DeCristo Daniela M.,Strande Natasha T.,Ramkissoon Lori,Milko Laura V.,Owen Phillips,Roy Sayanty,Xiong Mai,Paquin Ryan S.,Butterfield Rita M.,Lewis Megan A.,Souris Katherine J.,Bailey Donald B.,Rini Christine,Booker Jessica K.,Powell Bradford C.,Weck Karen E.,Powell Cynthia M.,Berg Jonathan S.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference109 articles.

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2. The tandem mass spectrometry newborn screening experience in North Carolina: 1997-2005;Frazier;J. Inherit. Metab. Dis.,2006

3. Impact of expanded newborn screening--United States, 2006;MMWR Morb. Mortal. Wkly. Rep.,2008

4. Clinical Applications of Mass Spectrometry Methods and Protocols;Hammett-Stabler,2010

5. Newborn screening: toward a uniform screening panel and system--executive summary;Watson;Pediatrics,2006

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