LAMM syndrome: two new patients with a novel mutation in FGF3 gene and additional clinical findings

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dc.contributor.authorBasdemirci, Muserref
dc.contributor.authorZamani, Ayse G.
dc.contributor.authorSener, Sevgi
dc.contributor.authorTassoker, Melek
dc.contributor.authorCetmili, Hayriye
dc.contributor.authorZamani, Adil
dc.contributor.authorAydogdu, Demet
dc.date.accessioned2024-02-23T14:21:13Z
dc.date.available2024-02-23T14:21:13Z
dc.date.issued2019
dc.departmentNEÜen_US
dc.description.abstract[Abstract Not Availabe]en_US
dc.identifier.doi10.1097/MCD.0000000000000254
dc.identifier.endpage85en_US
dc.identifier.issn0962-8827
dc.identifier.issn1473-5717
dc.identifier.issue2en_US
dc.identifier.pmid30433887en_US
dc.identifier.scopus2-s2.0-85062697488en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage81en_US
dc.identifier.urihttps://doi.org/10.1097/MCD.0000000000000254
dc.identifier.urihttps://hdl.handle.net/20.500.12452/13498
dc.identifier.volume28en_US
dc.identifier.wosWOS:000462177300007en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.ispartofClinical Dysmorphologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[Keyword Not Available]en_US
dc.titleLAMM syndrome: two new patients with a novel mutation in FGF3 gene and additional clinical findingsen_US
dc.typeArticleen_US

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