Clinical implications of del(20q) in patients with hematologic myeloid disorders.
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F02%3A00000135" target="_blank" >RIV/00023736:_____/02:00000135 - isvavai.cz</a>
Alternative codes found
RIV/00023736:_____/02:00000006
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Clinical implications of del(20q) in patients with hematologic myeloid disorders.
Original language description
Detection of 20q deletion using classical cytogenetic and molecular cytogenetic techniques in patients with myloid malignancies.
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
Result was created during the realization of more than one project. More information in the Projects tab.
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
European Journal of Human Genetics
ISSN
1018-4813
e-ISSN
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Volume of the periodical
10
Issue of the periodical within the volume
S1
Country of publishing house
GB - UNITED KINGDOM
Number of pages
1
Pages from-to
145
UT code for WoS article
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EID of the result in the Scopus database
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