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Mohr-Majewski syndrome (orofaciodigital syndrome type IV) in five sibs

dc.contributor.authorARAPOGLU, M
dc.contributor.authorCENANI, A
dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorSEVEN, Mehmet
dc.date.accessioned2021-03-05T21:13:10Z
dc.date.available2021-03-05T21:13:10Z
dc.date.issued1999
dc.identifier.citationTuysuz B., ARAPOGLU M., SEVEN M., CENANI A., "Mohr-Majewski syndrome (orofaciodigital syndrome type IV) in five sibs", GENETIC COUNSELING, cilt.10, ss.189-192, 1999
dc.identifier.issn1015-8146
dc.identifier.othervv_1032021
dc.identifier.otherav_d7df7241-a16e-402e-bc84-f0e528707784
dc.identifier.urihttp://hdl.handle.net/20.500.12627/142425
dc.description.abstractMohr-Majewski syndrome (orofaciodigital syndrome type IV) in five sibs: We present a girl and autopsy finding of her sister with Mohr-Majewski syndrome (Orofaciodigital syndrome type IV). The parents were first cousins and their two sons died of similar findings. The only healthy child of the family was mildly effected from this syndrome who had cleft palate. These features show the heterogenity of the syndrome.
dc.language.isoeng
dc.subjectTıbbi Ekoloji ve Hidroklimatoloji
dc.subjectYaşam Bilimleri
dc.subjectBiyoteknoloji
dc.subjectTemel Bilimler
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOTEKNOLOJİ VE UYGULAMALI MİKROBİYOLOJİ
dc.subjectMikrobiyoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTIBBİ ETİK
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTIP, ARAŞTIRMA VE DENEYSEL
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectTıp Eğitimi
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.titleMohr-Majewski syndrome (orofaciodigital syndrome type IV) in five sibs
dc.typeMakale
dc.relation.journalGENETIC COUNSELING
dc.contributor.department, ,
dc.identifier.volume10
dc.identifier.issue2
dc.identifier.startpage189
dc.identifier.endpage192
dc.contributor.firstauthorID9933


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