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Acrocallosal syndrome: report of five Turkish patients

dc.contributor.authorUlucan, H
dc.contributor.authorGul, D
dc.contributor.authorUnay, B
dc.contributor.authorAkin, R
dc.contributor.authorGokcay, E
dc.date.accessioned2021-03-06T08:49:05Z
dc.date.available2021-03-06T08:49:05Z
dc.date.issued2004
dc.identifier.citationGul D., Ulucan H., Unay B., Akin R., Gokcay E., "Acrocallosal syndrome: report of five Turkish patients", CLINICAL DYSMORPHOLOGY, cilt.13, ss.241-246, 2004
dc.identifier.issn0962-8827
dc.identifier.otherav_e2c9f6ab-d1d1-49e5-bf55-e100fa3d4bb4
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/149271
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/15365461
dc.identifier.urihttps://doi.org/10.1097/00019605-200410000-00008
dc.description.abstractAcrocallosal syndrome is characterized by agenesis of the corpus callosum, craniofacial anomalies, psychomotor retardation, and polydactyly. The clinical spectrum of this syndrome is broader than previous reports suggest Five Turkish patients including dizygotic twins are reported. (C) 2004 Lippincott Williams Wilkins.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleAcrocallosal syndrome: report of five Turkish patients
dc.typeMakale
dc.relation.journalCLINICAL DYSMORPHOLOGY
dc.contributor.department, ,
dc.identifier.volume13
dc.identifier.issue4
dc.identifier.startpage241
dc.identifier.endpage246
dc.contributor.firstauthorID728654


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