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Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly: A Further Patient With a 2-Year Follow-Up

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dc.authorscopusid18038773000
dc.authorscopusid56324033200
dc.authorscopusid57200644165
dc.authorscopusid16203264000
dc.authorscopusid13906055900
dc.authorscopusid6603432100
dc.contributor.authorSezer, O.
dc.contributor.authorGebesoglu, I.
dc.contributor.authorYuan, B.
dc.contributor.authorKaraca, E.
dc.contributor.authorGökçe, E.
dc.contributor.authorGüneş, S.
dc.date.accessioned2020-06-21T13:53:02Z
dc.date.available2020-06-21T13:53:02Z
dc.date.issued2014
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Sezer] Ozlem Türkeli,; [Gebesoglu] Ismet, Department of Pediatrics, Samsun Maternity and Child Health Hospital, Samsun, Turkey; [Yuan] Bo, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States; [Karaca] Ender, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States; [Gökçe] Erkan, Department of Radiology, Samsun Maternity and Child Health Hospital, Samsun, Turkey; [Güneş] Sezgin Özgür, Department of Medical Biology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.identifier.doi10.1097/MCD.0000000000000051
dc.identifier.endpage126en_US
dc.identifier.issn0962-8827
dc.identifier.issn1473-5717
dc.identifier.issue4en_US
dc.identifier.pmid25144151
dc.identifier.scopus2-s2.0-84906833360
dc.identifier.scopusqualityQ4
dc.identifier.startpage121en_US
dc.identifier.urihttps://doi.org/10.1097/MCD.0000000000000051
dc.identifier.volume23en_US
dc.identifier.wosWOS:000341627400002
dc.identifier.wosqualityQ4
dc.language.isoenen_US
dc.publisherLippincott Williams and Wilkins agents@lww.comen_US
dc.relation.ispartofClinical Dysmorphologyen_US
dc.relation.journalClinical Dysmorphologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleFibular Aplasia, Tibial Campomelia, and Oligosyndactyly: A Further Patient With a 2-Year Follow-Upen_US
dc.typeArticleen_US
dspace.entity.typePublication

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