rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
3
|
pubmed:dateCreated |
1998-1-29
|
pubmed:abstractText |
During a 13-year period, 22 children were treated for rhabdomyosarcoma (RMS). In 18 of these patients chromosome analysis was attempted on material from tumor biopsies, fine needle aspiration biopsies and/or bone marrow samples.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0098-1532
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
30
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
156-9
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9434823-Adolescent,
pubmed-meshheading:9434823-Child,
pubmed-meshheading:9434823-Child, Preschool,
pubmed-meshheading:9434823-Chromosome Aberrations,
pubmed-meshheading:9434823-Female,
pubmed-meshheading:9434823-Humans,
pubmed-meshheading:9434823-Infant,
pubmed-meshheading:9434823-Karyotyping,
pubmed-meshheading:9434823-Male,
pubmed-meshheading:9434823-Rhabdomyosarcoma
|
pubmed:year |
1998
|
pubmed:articleTitle |
Chromosomal aberrations in a consecutive series of childhood rhabdomyosarcoma.
|
pubmed:affiliation |
Department of Pediatric Surgery, University Hospital, Lund, Sweden. Carl-MagnusKullendorff@pedlund.Postnet.se
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|