Karen Grønskov

University of Copenhagen

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Scholarly Papers (1)

1.

Causal Germline Variants in Children with Cancer

Number of pages: 33 Posted: 15 Jul 2024
University of Copenhagen - Rigshospitalet, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Copenhagen University Hospital, Technical University of Denmark, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Department of Clinical Medicine, University of Copenhagen - Department of Clinical Immunology, University of Copenhagen - Copenhagen University Hospital, Aarhus University - Aarhus University Hospital, University of Copenhagen, Technical University of Denmark, Aarhus University - Aarhus University Hospital, Aarhus University - Aarhus University Hospital, Odense University Hospital, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Department of Pathology, University of Copenhagen - Copenhagen University Hospital, Aalborg University Hospital, Aalborg University Hospital, University of Copenhagen, University Hospital Rigshospitalet - Department of Paediatrics and Adolescent Medicine, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Department of Paediatrics and Adolescent Medicine, Massachusetts Institute of Technology and Harvard University - Broad Institute, University of Copenhagen, Massachusetts Institute of Technology and Harvard University - Broad Institute, University of Copenhagen - Copenhagen University Hospital, University of Copenhagen - Copenhagen University Hospital and University of Copenhagen - Department of Pediatrics and Adolescent Medicine
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Abstract:

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predisposition, pediatrics, evolution, genomics, next-generation sequencing, mutational constraint, clinical genetics