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Rethinking isolated cleft lip and palate as a syndrome.

dc.contributor.authorSeymen, Figen
dc.contributor.authorTuna, Elif Bahar
dc.contributor.authorGencay, Koray
dc.contributor.authorKoruyucu, Mine
dc.contributor.authorKasimoglu, Yelda
dc.contributor.authorBayram, Merve
dc.contributor.authorPATIR, ASLI
dc.contributor.authorErgoz, Nihan
dc.contributor.authorDeeley, Kathleen
dc.contributor.authorBussaneli, Diego
dc.contributor.authorModesto, Adriana
dc.contributor.authorVieira, Alexandre R.
dc.date.accessioned2021-03-04T09:38:56Z
dc.date.available2021-03-04T09:38:56Z
dc.date.issued2018
dc.identifier.citationKoruyucu M., Kasimoglu Y., Seymen F., Bayram M., PATIR A., Ergoz N., Tuna E. B. , Gencay K., Deeley K., Bussaneli D., et al., "Rethinking isolated cleft lip and palate as a syndrome.", Oral surgery, oral medicine, oral pathology and oral radiology, cilt.125, sa.4, ss.307-312, 2018
dc.identifier.issn2212-4403
dc.identifier.otherav_69373edd-bfee-4da5-bfed-17446e6c94fa
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/72906
dc.identifier.urihttps://doi.org/10.1016/j.oooo.2018.01.007
dc.description.abstractObjective. The goal of the present work was to use dental conditions that have been independently associated with cleft lip and palate (CL/P) as a tool to identify a broader collection of individuals to be used for gene identification that lead to clefts.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectDİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectDiş Hekimliği
dc.titleRethinking isolated cleft lip and palate as a syndrome.
dc.typeMakale
dc.relation.journalOral surgery, oral medicine, oral pathology and oral radiology
dc.contributor.departmentİstanbul Medipol Üniversitesi , ,
dc.identifier.volume125
dc.identifier.issue4
dc.identifier.startpage307
dc.identifier.endpage312
dc.contributor.firstauthorID252558


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