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Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta

dc.contributor.authorHAN, S. T.
dc.contributor.authorFiratli, E.
dc.contributor.authorOzdemir-Ozenen, D.
dc.contributor.authorSULIMA, P. P.
dc.contributor.authorHART, T. C.
dc.contributor.authorHART, P. S.
dc.contributor.authorBECERİK, SEMA
dc.contributor.authorÇOĞULU, DİLŞAH
dc.contributor.authorEMİNGİL, GÜLNUR
dc.date.accessioned2021-03-06T12:31:46Z
dc.date.available2021-03-06T12:31:46Z
dc.date.issued2009
dc.identifier.citationHART P. S. , BECERİK S., ÇOĞULU D., EMİNGİL G., Ozdemir-Ozenen D., HAN S. T. , SULIMA P. P. , Firatli E., HART T. C. , "Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta", CLINICAL GENETICS, cilt.75, ss.401-404, 2009
dc.identifier.issn0009-9163
dc.identifier.othervv_1032021
dc.identifier.otherav_f442fb55-5266-4af1-b6e8-43605cc21d5d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/160154
dc.identifier.urihttps://doi.org/10.1111/j.1399-0004.2008.01112.x
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.titleNovel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta
dc.typeMakale
dc.relation.journalCLINICAL GENETICS
dc.contributor.departmentNational Institutes of Health (NIH) - USA , ,
dc.identifier.volume75
dc.identifier.issue4
dc.identifier.startpage401
dc.identifier.endpage404
dc.contributor.firstauthorID37105


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