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AuthorYilmaz, Ruestemdc.contributor.author
AuthorSzakszon, Katalindc.contributor.author
AuthorAltmann, Annadc.contributor.author
AuthorAltunoglu, Umutdc.contributor.author
AuthorSenturk, Leylidc.contributor.author
AuthorMcGuire, Mariannedc.contributor.author
AuthorCalabrese, Olgadc.contributor.author
AuthorMadan-Khetarpal, Suneetadc.contributor.author
AuthorBasel-Vanagaite, Linadc.contributor.author
AuthorBorck, Guntramdc.contributor.author
Date of accession2019-09-16T05:56:42Zdc.date.accessioned
Available in OPARU since2019-09-16T05:56:42Zdc.date.available
Date of first publication2018dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
Dewey Decimal GroupDDC 570 / Life sciencesdc.subject.ddc
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleKaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patientsdc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Institut für Humangenetikuulm.affiliationSpecific
InstitutionInternationale Graduiertenschule für Molekulare Medizinuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1002/ajmg.a.38538dc.identifier.doiExternal
Source - Title of sourceAmerican Journal of Medical Genetics Part Asource.title
Source - Place of publicationWileysource.publisher
Source - Volume176source.volume
Source - Issue1source.issue
Source - Year2018source.year
Source - From page187source.fromPage
Source - To page193source.toPage
Source - ISSN1552-4825source.identifier.issn
Source - eISSN1552-4833source.identifier.eissn
Open AccessBronzeuulm.OA
Suitable communityUniversitätsklinikum Ulmuulm.community
Suitable communityZentrale Einrichtungenuulm.community
WoS000417872600026uulm.identifier.wos
University Bibliographyjauulm.unibibliographie


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