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dc.contributor.authorPercin, EF
dc.contributor.authorYilmaz, S
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:23:17Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:23:17Z
dc.date.issued2003
dc.identifier.issn0962-8827
dc.identifier.issn1473-5717
dc.identifier.urihttps://dx.doi.org/10.1097/01.mcd.0000081501.97834.1f
dc.identifier.urihttps://hdl.handle.net/20.500.12418/11335
dc.descriptionWOS: 000185870300016en_US
dc.descriptionPubMed ID: 14564221en_US
dc.description.abstractWe report on a case with polydactyly, syndactyly and brachydactyly of the hands and oligodactyly of the feet, but no other anomalies and normal chromosome analysis. We compared the findings in our case with those of brachydactyly B, Fuhrmann syndrome and Haas-type syndactyly. However, it was not possible to suggest a syndrome diagnosis in the present case.en_US
dc.language.isoengen_US
dc.publisherLIPPINCOTT WILLIAMS & WILKINSen_US
dc.relation.isversionof10.1097/01.mcd.0000081501.97834.1fen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectpolydactylyen_US
dc.subjectsyndactylyen_US
dc.subjectbrachydactylyen_US
dc.subjectoligodactylyen_US
dc.titleUnusual combination of limb malformations in the same patient: brachydactyly with syndactyly and postaxial polydactyly of the hands and postaxial oligodactyly of the feeten_US
dc.typeletteren_US
dc.relation.journalCLINICAL DYSMORPHOLOGYen_US
dc.contributor.departmentCumhuriyet Univ, Fac Med, Dept Med Biol & Genet, TR-58140 Sivas, Turkey -- Cumhuriyet Univ, Fac Med, Dept Plast & Reconstruct Surg, TR-58140 Sivas, Turkeyen_US
dc.contributor.authorIDPercin, Ferda -- 0000-0001-9317-8155en_US
dc.identifier.volume12en_US
dc.identifier.issue4en_US
dc.identifier.endpage284en_US
dc.identifier.startpage283en_US
dc.relation.publicationcategoryDiğeren_US


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