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AuthorCario, Hdc.contributor.author
AuthorSchwarz, Kdc.contributor.author
AuthorJorch, Ndc.contributor.author
AuthorKyank, Udc.contributor.author
AuthorPetrides, PEdc.contributor.author
AuthorSchneider, DTdc.contributor.author
AuthorUhle, Rdc.contributor.author
AuthorDebatin, Klaus-Michaeldc.contributor.author
AuthorKohne, Edc.contributor.author
Date of accession2018-06-18T07:56:31Zdc.date.accessioned
Available in OPARU since2018-06-18T07:56:31Zdc.date.available
Date of first publication2005dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
Keywordpolycythemiadc.subject
Keywordcongenital erythrocytosisdc.subject
Keywordvon-Hippel-Lindau genedc.subject
Keywordoxygen homeostasisdc.subject
Keywordhydroxyprolinedc.subject
Keywordrecognitiondc.subject
Keywordmutasedc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleMutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosisdc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Klinik für Kinder- und Jugendmedizinuulm.affiliationSpecific
InstitutionInstitut für Klinische Transfusionsmedizin und Immungenetik Ulm gGmbH (IKT)uulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
Source - Title of sourceHaematologicasource.title
Source - Place of publicationFerrata Storti Foundationsource.publisher
Source - Volume90source.volume
Source - Issue1source.issue
Source - Year2005source.year
Source - From page19source.fromPage
Source - To page24source.toPage
Source - ISSN0390-6078source.identifier.issn
Open Accessgolduulm.OA
Suitable communityUniversitätsklinikum Ulmuulm.community
Suitable communityWeitere Einrichtungenuulm.community
WoS000226501300004uulm.identifier.wos
University Bibliographyjauulm.unibibliographie


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