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AuthorGaspar, Haralddc.contributor.author
AuthorLutz, Bernddc.contributor.author
AuthorReicherter, Kerstindc.contributor.author
AuthorLuehl, Simondc.contributor.author
AuthorTaurman, Ritadc.contributor.author
AuthorGabriel, Heinzdc.contributor.author
AuthorBrenner, Rolf E.dc.contributor.author
AuthorBorck, Guntramdc.contributor.author
Date of accession2018-12-18T12:24:34Zdc.date.accessioned
Available in OPARU since2018-12-18T12:24:34Zdc.date.available
Date of first publication2017dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
Keywordthoracic aortic-aneurysmdc.subject
Keywordmarfan-syndromedc.subject
Keywordsyndrome type-4dc.subject
Keywordbeta receptordc.subject
Keywordbone massdc.subject
Keywordmutationsdc.subject
Keyworddissectionsdc.subject
Keywordphenotypedc.subject
Keywordgenedc.subject
Keywordidentificationdc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
Title4.7 Mb deletion encompassing TGFB2 associated with features of Loeys-Dietz syndrome and osteoporosis in adulthooddc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Institut für Humangenetikuulm.affiliationSpecific
InstitutionUKU. Klinik für Orthopädieuulm.affiliationSpecific
InstitutionUKU. Klinik für Kinder- und Jugendmedizinuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1002/ajmg.a.38286dc.identifier.doiExternal
Source - Title of sourceAmerican Journal of Medical Genetics Part Asource.title
Source - Place of publicationWileysource.publisher
Source - Volume173source.volume
Source - Issue8source.issue
Source - Year2017source.year
Source - From page2289source.fromPage
Source - To page2292source.toPage
Source - ISSN1552-4825source.identifier.issn
Source - eISSN1552-4833source.identifier.eissn
CommunityUniversitätsklinikum Ulmuulm.community
WoS000407838900032uulm.identifier.wos
Bibliographyuulmuulm.bibliographie


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