Chromosome 17 abnormalities in pediatric neuroblastic tumor with abundant neuropil and true rosettes

American Journal of Clinical Pathology

Volumn 126, Issue 2, 2006, Pages 277-283

  Fuller, Christine ^a,b   Fouladi, Maryam ^a   Gajjar, Amar ^a   Dalton, James ^a   Sanford, R Alex ^a   Helton, Kathleen J ^a  

^a ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

^b WILLIAM BEAUMONT HOSPITAL   (United States)

Author keywords

Fluorescence in situ hybridization; Isochromosome 17q i(17q) ; Neuroblastic; Neuropil; Pediatric; Rosettes

Indexed keywords

ANTINEOPLASTIC AGENT;

ARTICLE; BRAIN TUMOR; CANCER CHEMOTHERAPY; CANCER RADIOTHERAPY; CASE REPORT; CELL DIFFERENTIATION; CELL STRUCTURE; CENTRAL NERVOUS SYSTEM TUMOR; CHILDHOOD CANCER; CHROMOSOME 17; CHROMOSOME ABERRATION; CYTOREDUCTIVE SURGERY; FEMALE; GENE AMPLIFICATION; GENE DELETION; HISTOLOGY; HUMAN; HUMAN TISSUE; ISOCHROMOSOME; MALE; MEDULLOBLASTOMA; MICROSCOPY; NEUROPIL; ONCOGENE; ONCOGENE MYC; ONCOGENE MYCN; PEDIATRIC NEUROBLASTIC TUMOR WITH ABUNDANT NEUROPIL AND TRUE ROSETTES; POLYSOMY 17; PONS ANGLE TUMOR; PRESCHOOL CHILD; PRIORITY JOURNAL; RARE DISEASE; ROSETTE FORMATION; TUMOR CLASSIFICATION;

EID: 33746706925     PISSN: 00029173     EISSN: None     Source Type: Journal    
DOI: 10.1309/TFBX1LWQ93MXQBAW     Document Type: Article

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