Ewing sarcoma and sinonasal neuroectodermal tumors as second malignant tumors after retinoblastoma and other neoplasms

Medical and Pediatric Oncology

Volumn 36, Issue 2, 2001, Pages 290-294

  Cope, Judith U ^a   Tsokos, Maria ^a   Miller, Robert W ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

Author keywords

Ewing sarcoma; Olfactory neuroblastoma; RB 1 gene; Retinoblastoma; Second malignant neoplasms; Sinonasal neuroectodermal tumors

Indexed keywords

PROTEIN; PROTEIN MIC 2; UNCLASSIFIED DRUG;

ARTICLE; CANCER SUSCEPTIBILITY; CHILDHOOD CANCER; ESTHESIONEUROBLASTOMA; EWING SARCOMA; HERITABILITY; HISTOLOGY; HUMAN; IMMUNOHISTOCHEMISTRY; NEUROECTODERM TUMOR; OSTEOSARCOMA; PRIORITY JOURNAL; RETINOBLASTOMA; SECOND CANCER; SOFT TISSUE SARCOMA; TUMOR SUPPRESSOR GENE;

ADOLESCENT; AGE FACTORS; CHILD; CHILD, PRESCHOOL; FEMALE; GENES, RETINOBLASTOMA; HUMANS; MALE; NEOPLASMS, SECOND PRIMARY; NEUROECTODERMAL TUMORS; NOSE NEOPLASMS; RADIOTHERAPY; RETINAL NEOPLASMS; RETINOBLASTOMA; SARCOMA, EWING'S;

EID: 0035140690     PISSN: 00981532     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-911X(20010201)36:2<290::AID-MPO1067>3.0.CO;2-5     Document Type: Article

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