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Paper Details

Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group.
Fam Cancer
18
2021
ATRT, Atypical Teratoid Rhabdoid Tumors, BAF chromatin remodeling complex, Coffin-Siris Syndrome, Host Genome, PVs, RT, RTPS, RTPS1, RTPS1 and 2, RTPS1&2, RTPS2, SCCOHT, SMARCA4, SMARCB1, cancer, children, genetic conditions, genetic disorders, malignant neoplasms, rhabdoid tumor, rhabdoid tumor (RT) predisposition syndromes 1 and 2, small cell carcinoma of the ovaries, hypercalcemic type, tumor
Author NameAffiliation
Michael C FrühwaldSwabian Children's Cancer Center, University Medical Center Augsburg
Heidrun BoztugSt. Anna Children's Hospital and Children's Cancer Research Institute, Medical University of Vienna
Christian P KratzHannover Medical School
Kristian W PajtlerHopp Children's Cancer Center Heidelberg (KiTZ)
Kristian W PajtlerHopp Children's Cancer Center Heidelberg (KiTZ)
Kristian W PajtlerUniversity Hospital Heidelberg
Kristian W PajtlerGerman Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK)
Kristian W PajtlerChildren's Hospital, University of Helsinki and Helsinki University Hospital
Kristian W PajtlerChildren's Hospital, University of Helsinki and Helsinki University Hospital
Kristian W PajtlerGerman Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK)
Kristian W PajtlerUniversity Hospital Heidelberg
Franck BourdeautInstitut Curie, SIREDO Pediatric Cancer Center, INSERM U, Paris Sciences Lettres Research University
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Release 1.2