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AuthorKarges, Bdc.contributor.author
AuthorLeHeup, Bdc.contributor.author
AuthorSchoenle, Edc.contributor.author
AuthorCastro-Correia, Cdc.contributor.author
AuthorFontoura, Mdc.contributor.author
AuthorPfaffle, Rdc.contributor.author
AuthorAndler, Wdc.contributor.author
AuthorDebatin, Klaus-Michaeldc.contributor.author
AuthorKarges, Wdc.contributor.author
Date of accession2018-06-18T09:20:26Zdc.date.accessioned
Available in OPARU since2018-06-18T09:20:26Zdc.date.available
Date of first publication2004dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
Keywordhypothyroidismdc.subject
KeywordTSH deficiencydc.subject
Keywordgene mutationsdc.subject
Keywordneonatal screeningdc.subject
Keywordalleledc.subject
Keywordpituitary-hormone deficiencydc.subject
Keywordsubunit genedc.subject
Keywordsecondary hypothyroidismdc.subject
Keywordthyrotropindc.subject
Keywordfamiliesdc.subject
Keywordchildrendc.subject
Keywordreceptordc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleCompound heterozygous and homozygous mutations of the TSH beta gene as a cause of congenital central hypothyroidism in Europedc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Klinik für Kinder- und Jugendmedizinuulm.affiliationSpecific
InstitutionUKU. Klinik für Innere Medizin Iuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1159/000080071dc.identifier.doiExternal
Source - Title of sourceHormone Researchsource.title
Source - Place of publicationKarger Publisherssource.publisher
Source - Volume62source.volume
Source - Issue3source.issue
Source - Year2004source.year
Source - From page149source.fromPage
Source - To page155source.toPage
Source - ISSN0301-0163source.identifier.issn
Open AccessNouulm.OA
CommunityUniversitätsklinikum Ulmuulm.community
WoS000223757700008uulm.identifier.wos
Bibliographyuulmuulm.bibliographie


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