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A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia

dc.contributor.authorYosunkaya, Elif
dc.contributor.authorOzen, Mustafa
dc.contributor.authorKoparir, Erkan
dc.contributor.authorGezdirici, Alper
dc.contributor.authorYuksel, Adnan
dc.contributor.authorYENİGÜN, Alper
dc.contributor.authorSeven, Mehmet
dc.contributor.authorUlucan, Hakan
dc.date.accessioned2021-03-04T10:59:38Z
dc.date.available2021-03-04T10:59:38Z
dc.date.issued2013
dc.identifier.citationGezdirici A., YENİGÜN A., Koparir E., Yosunkaya E., Ulucan H., Seven M., Yuksel A., Ozen M., "A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia", CLINICAL DYSMORPHOLOGY, cilt.22, sa.1, ss.33-35, 2013
dc.identifier.issn0962-8827
dc.identifier.othervv_1032021
dc.identifier.otherav_70059651-5c69-40c1-8d53-0f2af0afe0a2
dc.identifier.urihttp://hdl.handle.net/20.500.12627/77251
dc.identifier.urihttps://doi.org/10.1097/mcd.0b013e32835b8e6e
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleA rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia
dc.typeMakale
dc.relation.journalCLINICAL DYSMORPHOLOGY
dc.contributor.departmentBezmiâlem Vakıf Üniversitesi , Tıp Fakültesi , Cerrahi Tıp Bilimleri Bölümü
dc.identifier.volume22
dc.identifier.issue1
dc.identifier.startpage33
dc.identifier.endpage35
dc.contributor.firstauthorID14862


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