Lack of genotype-phenotype correlation for Kindlin-1 mutations in Kindler syndrome and evidence for possible genetic heterogeneity

Basit Öğe Kaydı
dc.contributor.authorLai-Cheong, J.
dc.contributor.authorLiu, L.
dc.contributor.authorTaskesen, M.
dc.contributor.authorAkdeniz, S.
dc.contributor.authorMaari, C.
dc.contributor.authorEmanuel, P.
dc.contributor.authorMcGrath, J. A.
dc.date.accessioned2024-04-24T17:49:50Z
dc.date.available2024-04-24T17:49:50Z
dc.date.issued2008
dc.departmentDicle Üniversitesien_US
dc.description88th Annual Meeting of the British-Association-of-Dermatologists -- JUL 01-04, 2008 -- Liverpool, ENGLANDen_US
dc.description.abstract[Abstract Not Available]en_US
dc.description.sponsorshipBritish Assoc Dermatologistsen_US
dc.identifier.endpage12en_US
dc.identifier.issn0007-0963
dc.identifier.startpage11en_US
dc.identifier.urihttps://hdl.handle.net/11468/23016
dc.identifier.volume159en_US
dc.identifier.wosWOS:000256497700021
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.relation.ispartofBritish Journal of Dermatology
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keyword]en_US
dc.titleLack of genotype-phenotype correlation for Kindlin-1 mutations in Kindler syndrome and evidence for possible genetic heterogeneityen_US
dc.titleLack of genotype-phenotype correlation for Kindlin-1 mutations in Kindler syndrome and evidence for possible genetic heterogeneity
dc.typeConference Objecten_US

Dosyalar

Koleksiyon

WoS İndeksli Yayınlar Koleksiyonu