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Paper Details

A toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing.
J Genet Couns
9
2019
ES, Undiagnosed, patient, patients, rare diseases
Author NameAffiliation
Jennefer N KohlerCenter for Undiagnosed Diseases, Stanford University
Liliana FernandezCenter for Undiagnosed Diseases, Stanford University
Megan E GroveClinical Genomics Program
Dianna G FiskClinical Genomics Program
Yaping YangBaylor College of Medicine
David BickHudsonAlpha Institute for Biotechnology
David BickHudsonAlpha Institute for Biotechnology
Elizabeth A WortheyHudsonAlpha Institute for Biotechnology
Elizabeth A WortheyHudsonAlpha Institute for Biotechnology
Paul G FisherCenter for Undiagnosed Diseases, Stanford University
Paul G FisherStanford University School of Medicine
Paul G FisherStanford University School of Medicine
Euan A AshleyCenter for Undiagnosed Diseases, Stanford University
Euan A AshleyStanford University School of Medicine
Euan A AshleyStanford University School of Medicine
Euan A AshleyClinical Genomics Program
Jonathan A BernsteinCenter for Undiagnosed Diseases, Stanford University
Jonathan A BernsteinStanford University School of Medicine
Matthew T WheelerCenter for Undiagnosed Diseases, Stanford University
Matthew T WheelerStanford University School of Medicine
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Release 1.2