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Paper Details

Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts.
Front Genet
8
2014
CNVs, copy number variations, rare diseases
Author NameAffiliation
John J ConnollyThe Center for Applied Genomics, Children's Hospital of Philadelphia Philadelphia
Joseph T GlessnerThe Center for Applied Genomics, Children's Hospital of Philadelphia Philadelphia, University of Pennsylvania Perelman School of Medicine Philadelphia
Berta AlmogueraThe Center for Applied Genomics, Children's Hospital of Philadelphia Philadelphia
David R CrosslinUniversity of Washington Medical Center Seattle
David R CrosslinUniversity of Washington Medical Center Seattle
Gail P JarvikUniversity of Washington Medical Center Seattle
Gail P JarvikUniversity of Washington Medical Center Seattle
Patrick M A SleimanThe Center for Applied Genomics, Children's Hospital of Philadelphia Philadelphia, University of Pennsylvania Perelman School of Medicine Philadelphia
Patrick M A SleimanThe Center for Applied Genomics, Children's Hospital of Philadelphia Philadelphia, University of Pennsylvania Perelman School of Medicine Philadelphia
Hakon HakonarsonThe Center for Applied Genomics, Children's Hospital of Philadelphia Philadelphia, University of Pennsylvania Perelman School of Medicine Philadelphia
Hakon HakonarsonThe Center for Applied Genomics, Children's Hospital of Philadelphia Philadelphia, University of Pennsylvania Perelman School of Medicine Philadelphia
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