Congenital disseminated malignant rhabdoid tumor: A distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11

American Journal of Surgical Pathology

Volumn 23, Issue 3, 1999, Pages 249-256

  White, Frances V ^a   Dehner, Louis P ^a   Belchis, Deborah A ^b   Conard, Katrina ^c   Davis, Mary M ^d   Stocker, J Thomas ^e   Zuppan, Craig W ^f   Biegel, Jaclyn A ^g   Perlman, Elizabeth J ^h  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b PENN STATE COLLEGE OF MEDICINE   (United States)

^c NEMOURS ALFRED I DUPONT HOSPITAL FOR CHILDREN   (United States)

^d INDIANA UNIVERSITY MEDICAL CENTER   (United States)

^e UNIFORMED SERVICES UNIVERSITY OF THE HEALTH SCIENCES   (United States)

^f LOMA LINDA UNIVERSITY   (United States)

^g CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^h DEPARTMENT OF PATHOLOGY   (United States)

Author keywords

Chromosome 22; Congenital tumors; Malignant rhabdoid tumor; Placenta metastasis

Indexed keywords

ARTICLE; CHROMOSOME 22Q; CHROMOSOME ABERRATION; CLINICAL ARTICLE; CONGENITAL TUMOR; ELECTRON MICROSCOPY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INFANT; KARYOTYPE; MALE; NEWBORN; RHABDOID TUMOR; SURVIVAL RATE; TUMOR LOCALIZATION;

CHROMOSOMES, HUMAN, PAIR 22; CYTOSKELETON; FEMALE; GENE DELETION; GESTATIONAL AGE; HEAD AND NECK NEOPLASMS; HUMANS; IMMUNOENZYME TECHNIQUES; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE; PROGNOSIS; RHABDOID TUMOR;

EID: 0033055970     PISSN: 01475185     EISSN: None     Source Type: Journal    
DOI: 10.1097/00000478-199903000-00001     Document Type: Article

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