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Paper Details

High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations.
Transl Res
0
2024
191, BD, BDs, Birth Defects, CNV loci, CNVs, ChrX:52,863,011-55,652,521, E2F target genes, P, P/LP, P/LP CNVs, Patients, Pediatric Cancers, birth defects, cancer, cancers, genetic defects, patients, pediatric cancers, pediatric onset cancers
Author NameAffiliation
Joseph T GlessnerCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, The Perelman School of Medicine, University of Pennsylvania
Frank D MentchCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia
Frank D MentchCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia
John J ConnollyCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia
Hakon HakonarsonCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, The Perelman School of Medicine, University of Pennsylvania, University of Iceland
Hakon HakonarsonCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, The Perelman School of Medicine, University of Pennsylvania, University of Iceland
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