Elejalde syndrome - A case report
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F06%3A87" target="_blank" >RIV/00216208:11130/06:87 - isvavai.cz</a>
Alternative codes found
RIV/00843989:_____/06:00013350
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Elejalde syndrome - A case report
Original language description
Elejalde syndrome (McKusick 200995), also known as acrocephalopolydactylous dysplasia, is a rare condition. We describe a sixth patient with this syndrome which is characterized by craniosynostosis and hyperproliferation of fibroblasts in many tissues in
Czech name
Elejalde syndrom - popis případu
Czech description
Elejalde syndrom (McKusick 200995), známý jako dysplasie s akrocefalopolydaktylií, je vzácné onemocnění. Popisujeme šestý případ tohoto syndromu, který je charakterizován kraniosynostosou a hyperproliferací fibroblastů v mnoha tkáních.
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EB - Genetics and molecular biology
OECD FORD branch
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Result continuities
Project
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Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2006
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
American Journal of Medical Genetics. Part A
ISSN
1552-4825
e-ISSN
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Volume of the periodical
140A
Issue of the periodical within the volume
20
Country of publishing house
US - UNITED STATES
Number of pages
4
Pages from-to
2223-2226
UT code for WoS article
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EID of the result in the Scopus database
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