HANHART SYNDROME

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dc.authoridYakıncı, Mehmet Cengiz/0000-0001-5930-4269
dc.authoridAslan, Mehmet/0000-0001-5710-6592
dc.authoridDogan, Derya Gumus/0000-0003-1587-9639
dc.authorwosidYakıncı, Mehmet Cengiz/ABI-7519-2020
dc.authorwosidAslan, Mehmet/AEL-7823-2022
dc.authorwosidDogan, Derya Gumus/ABG-9945-2020
dc.contributor.authorDogan, D. G.
dc.contributor.authorDogan, M.
dc.contributor.authorAslan, M.
dc.contributor.authorMenekse, E.
dc.contributor.authorYakinci, C.
dc.date.accessioned2024-08-04T20:32:40Z
dc.date.available2024-08-04T20:32:40Z
dc.date.issued2010
dc.departmentİnönü Üniversitesien_US
dc.description.abstractHanhart syndrome: We report on a male infant with Hanhart Syndrome. It is classified in oromandibular limb hypogenesis syndromes which are a group of rare conditions involving congenital malformations of tongue, mandible, and limbs.en_US
dc.identifier.endpage362en_US
dc.identifier.issn1015-8146
dc.identifier.issue4en_US
dc.identifier.pmid21290964en_US
dc.identifier.scopus2-s2.0-78650719730en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage359en_US
dc.identifier.urihttps://hdl.handle.net/11616/95224
dc.identifier.volume21en_US
dc.identifier.wosWOS:000285490900001en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherMedecine Et Hygieneen_US
dc.relation.ispartofGenetic Counselingen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHanhart Syndromeen_US
dc.subjectHypoglossiaen_US
dc.subjectHypodactiliaen_US
dc.titleHANHART SYNDROMEen_US
dc.typeArticleen_US

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