FANCC and PTCH1 gene loss in congenital infantile rhabdomyosarcoma with spindle cell features

Pediatr Blood Cancer. 2023 Apr;70(4):e30083. doi: 10.1002/pbc.30083. Epub 2022 Nov 3.

Authors

Kei Shing Oh¹, Ferial Alloush¹, Maggie Fader², Carole Brathwaite³

Affiliations

¹ Arkadi M. Rywlin M.D. Department of Pathology and Laboratory Medicine, Mount Sinai Medical Center, Miami Beach, Florida, USA.
² Pediatric Hematology/Oncology, Nicklaus Children's Hospital, Miami's Children's Health System, Miami, Florida, USA.
³ Department of Pathology and Laboratory Medicine, Nicklaus Children's Hospital, Miami's Children's Health System, Miami, Florida, USA.

PMID: 36326135
DOI: 10.1002/pbc.30083

No abstract available

Publication types

Letter

MeSH terms

Fanconi Anemia Complementation Group C Protein / genetics
Humans
Rhabdomyosarcoma* / genetics

Substances

FANCC protein, human
Fanconi Anemia Complementation Group C Protein