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dc.contributor.authorAkan, M
dc.contributor.authorAkoz, T
dc.contributor.authorDeviren, A
dc.contributor.authorYildirim, S
dc.date.accessioned2021-03-04T11:44:02Z
dc.date.available2021-03-04T11:44:02Z
dc.date.issued2002
dc.identifier.citationYildirim S., Akan M., Deviren A., Akoz T., "Penile agenesis and clavicular anomaly in a child with an oral facial digital syndrome", CLINICAL DYSMORPHOLOGY, cilt.11, sa.1, ss.29-32, 2002
dc.identifier.issn0962-8827
dc.identifier.otherav_73ceedf4-3b69-40f2-b454-b847b0a8e349
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/79619
dc.identifier.urihttps://doi.org/10.1097/00019605-200201000-00006
dc.description.abstractWe report a male patient with the clinical characteristics of an OFDS (oral facial digital syndrome). He also has penile agenesis, clavicular flattening and cerebellar anomalies. This patient was classified as a severe form of OFD type II-Mohr syndrome but the possibility of this being OFDS VI-Varadi syndrome or a new form of OFDS cannot completely be excluded.
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titlePenile agenesis and clavicular anomaly in a child with an oral facial digital syndrome
dc.typeMakale
dc.relation.journalCLINICAL DYSMORPHOLOGY
dc.contributor.department, ,
dc.identifier.volume11
dc.identifier.issue1
dc.identifier.startpage29
dc.identifier.endpage32
dc.contributor.firstauthorID164138


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