Rhabdomyosarcoma, osteosarcoma, and adrenocortical carcinoma in a child with a germline p53 mutation

Pediatric Blood and Cancer

Volumn 43, Issue 6, 2004, Pages 683-686

  Khayat, Catherine M ^a   Johnston, Donna L ^a  

^a CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

Author keywords

Adrenocortical carcinoma; Li Fraumeni syndrome; Osteosarcoma; p53 mutation; Rhabdomyosarcoma

Indexed keywords

ANTINEOPLASTIC AGENT; CYCLOPHOSPHAMIDE; DACTINOMYCIN; DNA; GLUCOCORTICOID; MINERALOCORTICOID; MITOTANE; PRASTERONE; PRASTERONE SULFATE; PROTEIN P53; VINCRISTINE;

ABDOMINAL MASS; ADRENAL CORTEX CARCINOMA; ADRENAL INSUFFICIENCY; ADRENAL SUPPRESSION; ARTICLE; BONE BIOPSY; CASE REPORT; CHEMOTHERAPY INDUCED EMESIS; CHILDHOOD CANCER; COMPUTER ASSISTED TOMOGRAPHY; DNA SEQUENCE; FAMILIAL CANCER; GENE MUTATION; HUMAN; JAW CANCER; MULTIPLE CANCER; NAUSEA; NUCLEAR MAGNETIC RESONANCE IMAGING; OSTEOSARCOMA; PRESCHOOL CHILD; PRIORITY JOURNAL; RHABDOMYOSARCOMA; VIRILIZATION; VOMITING;

ADRENAL CORTEX NEOPLASMS; CHILD; FOLLOW-UP STUDIES; GERM-LINE MUTATION; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; OSTEOSARCOMA; RHABDOMYOSARCOMA; TOMOGRAPHY SCANNERS, X-RAY COMPUTED; TUMOR SUPPRESSOR PROTEIN P53;

EID: 6944253452     PISSN: 15455009     EISSN: None     Source Type: Journal    
DOI: 10.1002/pbc.20142     Document Type: Article

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