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Paper Details

Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development.
Mol Cancer
0
2023
3'UTR regions, 5' UTR variants, BD, BD-cancer, Children, Genomic variants, Intronic variants, birth defects, blood, cancer, cancers, children, chromosomal anomalies, exon, exons, genomic regions, introns, malignant tumors, ncRNA, ncRNAs, ncRNAs exons, non-coding RNA, patients, prior exons locus, protein, protein-, protein-coding/ncRNA, protein-coding/ncRNAs, recurrent variants, splicing site
Author NameAffiliation
Frank D MentchCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia
Frank D MentchCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia
Xiang WangCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia
Joseph T GlessnerCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia
Joseph T GlessnerThe Perelman School of Medicine, University of Pennsylvania
Hakon HakonarsonCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia
Hakon HakonarsonThe Perelman School of Medicine, University of Pennsylvania
Hakon HakonarsonChildren's Hospital of Philadelphia
Hakon HakonarsonChildren's Hospital of Philadelphia
Hakon HakonarsonUniversity of Iceland
Hakon HakonarsonCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia
Hakon HakonarsonThe Perelman School of Medicine, University of Pennsylvania
Hakon HakonarsonChildren's Hospital of Philadelphia
Hakon HakonarsonChildren's Hospital of Philadelphia
Hakon HakonarsonUniversity of Iceland
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