Additional evidence of genetic changes in children with ALL and TEL/AML1 fusion gene
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F02%3A00000601" target="_blank" >RIV/61989592:15110/02:00000601 - isvavai.cz</a>
Alternative codes found
RIV/61989592:15110/02:00006154
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Additional evidence of genetic changes in children with ALL and TEL/AML1 fusion gene
Original language description
Our observation confirms the existence of further secondary chromosomal changes, eg. duplication of TEL/AML1 fusion gene at the time of diagnosis of ALL, which may also contribute to the process of leukemogenesis
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FD - Oncology and haematology
OECD FORD branch
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Result continuities
Project
<a href="/en/project/NE6188" target="_blank" >NE6188: Study of cryptic chromosomal regions involved into complex translocations in acute leukem. and myelodysplastic syndrome by multicolour fluoresc. in situ hybridisation (M-FISH).</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2002
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Leukemia
ISSN
0887-6924
e-ISSN
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Volume of the periodical
16
Issue of the periodical within the volume
9
Country of publishing house
GB - UNITED KINGDOM
Number of pages
3
Pages from-to
1873-1875
UT code for WoS article
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EID of the result in the Scopus database
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