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Omani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3

dc.contributor.authorMizumoto, S.
dc.contributor.authorCELEBI, A.
dc.contributor.authorSugahara, K.
dc.contributor.authorTURKMEN, Solmaz
dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorMUNDLOS, S.
dc.date.accessioned2021-03-04T10:08:34Z
dc.date.available2021-03-04T10:08:34Z
dc.date.issued2009
dc.identifier.citationTuysuz B., Mizumoto S., Sugahara K., CELEBI A., MUNDLOS S., TURKMEN S., "Omani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3", CLINICAL GENETICS, cilt.75, sa.4, ss.375-383, 2009
dc.identifier.issn0009-9163
dc.identifier.othervv_1032021
dc.identifier.otherav_6bb4fc03-55f3-4297-9d18-dd8677eb124c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/74479
dc.identifier.urihttps://doi.org/10.1111/j.1399-0004.2009.01167.x
dc.description.abstractTuysuz B, Mizumoto S, Sugahara K, Celebi A, Mundlos S, Turkmen S. Omani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3.Clin Genet 2009: 75: 375-383. (C) Blackwell Munksgaard, 2009
dc.language.isoeng
dc.subjectTıp
dc.subjectTemel Bilimler
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri
dc.subjectTıbbi Genetik
dc.subjectDahili Tıp Bilimleri
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectSağlık Bilimleri
dc.titleOmani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3
dc.typeMakale
dc.relation.journalCLINICAL GENETICS
dc.contributor.departmentHokkaido Üniversitesi , ,
dc.identifier.volume75
dc.identifier.issue4
dc.identifier.startpage375
dc.identifier.endpage383
dc.contributor.firstauthorID9477


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