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Paper Details

ANKRD11 variants: KBG syndrome and beyond.
Clin Genet
18
2021
Author NameAffiliation
Yiran GuoCenter for Applied Genomics and Center for Data Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Yiran GuoCenter for Applied Genomics and Center for Data Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Denise HornInstitute of Medical and Human Genetics, Charite-Universitatsmedizin Berlin
Sally Ann Lynch
Angelo SelicorniCentro Fondazione Mariani per il Bambino Fragile ASST-Lariana Sant'Anna Hospital
Elaine H ZackaiChildren's Hospital of Philadelphia
Elaine H ZackaiChildren's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania
Giuseppe ZampinoCenter for Rare Diseases and Birth Defects, Fondazione Policlinico Universitario A. Gemelli IRCCS
Hakon HakonarsonCenter for Applied Genomics and Center for Data Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Hakon HakonarsonChildren's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania
Hakon HakonarsonCenter for Applied Genomics and Center for Data Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Hakon HakonarsonChildren's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania
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