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Whole-genome sequencing for identification of Mendelian d... | ResearchHub
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Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings
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Authors
Laurel Willig
23 more
Laurel Willig
•
Josh Petrikin
21 more
•
Stephen Kingsmore
Published
April 28, 2015
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Journal
The Lancet Respiratory Medicine
Topics
Medicine
Immunology
Pathology
Internal Medicine
Pediatrics
Show all topics
DOI
10.1016/s2213-2600(15)00139-3
Other Formats
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Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
The Lancet Respiratory Medicine
Topics
Medicine
Immunology
Pathology
Internal Medicine
Pediatrics
Show all topics
DOI
10.1016/s2213-2600(15)00139-3
Other Formats
PDF
