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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2004-4-15
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pubmed:abstractText |
Atypical teratoid/rhabdoid tumours (AT/RT) are highly malignant embryonal tumours of the brain composed of rhabdoid cells. Inactivating mutations of the hSNF5/INI-1 gene located in the chromosomal region 22q11.2 are regarded as a crucial step in their molecular pathogenesis. Apart from monosomy or deletions of chromosome 22 not much data exists on additional chromosomal aberrations.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0256-7040
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pubmed:author |
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pubmed:copyrightInfo |
Copyright 2004 Springer-Verlag
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pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
221-4
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14767597-Brain Neoplasms,
pubmed-meshheading:14767597-Child, Preschool,
pubmed-meshheading:14767597-Chromosomal Proteins, Non-Histone,
pubmed-meshheading:14767597-Chromosome Aberrations,
pubmed-meshheading:14767597-Chromosomes, Human, Pair 22,
pubmed-meshheading:14767597-DNA-Binding Proteins,
pubmed-meshheading:14767597-Female,
pubmed-meshheading:14767597-Humans,
pubmed-meshheading:14767597-Infant,
pubmed-meshheading:14767597-Infant, Newborn,
pubmed-meshheading:14767597-Male,
pubmed-meshheading:14767597-Mutation,
pubmed-meshheading:14767597-Nucleic Acid Hybridization,
pubmed-meshheading:14767597-Rhabdoid Tumor,
pubmed-meshheading:14767597-Transcription Factors
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pubmed:year |
2004
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pubmed:articleTitle |
Chromosomal imbalances detected by comparative genomic hybridisation in atypical teratoid/rhabdoid tumours.
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pubmed:affiliation |
Institute of Pathology, University Hospital Münster, Domagkstrasse 17, 48149 Münster, Germany. rickchr@uni-muenster.de
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pubmed:publicationType |
Journal Article,
Comparative Study
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