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Paper Details

Long-read genome sequencing identifies causal structural variation in a Mendelian disease.
Genet Med
146
2018
Author NameAffiliation
Jason D MerkerStanford University
Jason D MerkerStanford Medicine Clinical Genomics Service
Aaron M Wenger
Megan E GroveStanford Medicine Clinical Genomics Service
Zachary ZappalaStanford University
Zachary ZappalaStanford University
Zachary ZappalaStanford University
Zachary ZappalaStanford University
Laure Fr??sardStanford University
Daryl WaggottStanford University
Daryl WaggottStanford Center for Inherited Cardiovascular Disease, Stanford University
Kevin S SmithStanford University
Kevin S SmithStanford University
Stephen B MontgomeryStanford University
Stephen B MontgomeryStanford University
Stephen B MontgomeryStanford University
Stephen B MontgomeryStanford University
Matthew T WheelerStanford University
Matthew T WheelerStanford Center for Inherited Cardiovascular Disease, Stanford University
Matthew T WheelerStanford University
Matthew T WheelerStanford Center for Inherited Cardiovascular Disease, Stanford University
James M FordStanford University
James M FordStanford Cancer Institute
James M FordStanford University
Euan A AshleyStanford Medicine Clinical Genomics Service
Euan A AshleyStanford University
Euan A AshleyStanford University
Euan A AshleyStanford Center for Inherited Cardiovascular Disease, Stanford University
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