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dc.contributor.authorZeybek, C
dc.contributor.authorUngur, S
dc.contributor.authorZorer, G
dc.contributor.authorSipahi, O
dc.contributor.authorTuysuz, B
dc.date.accessioned2021-03-05T16:34:34Z
dc.date.available2021-03-05T16:34:34Z
dc.date.issued2002
dc.identifier.citationTuysuz B., Zeybek C., Zorer G., Sipahi O., Ungur S., "Patient with the mesomelic dysplasia, Nievergelt syndrome, and cerebellovermian agenesis and cataracts", AMERICAN JOURNAL OF MEDICAL GENETICS, cilt.109, ss.206-210, 2002
dc.identifier.issn0148-7299
dc.identifier.otherav_c14a36d1-7260-43f8-a755-de78dd8d3f5b
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/128283
dc.identifier.urihttps://doi.org/10.1002/ajmg.10283
dc.description.abstractWe describe a 33-day-old boy who had short and thick tibiae, symmetrical oligosyndactyly of the hands, and distinctive face. The patient was considered as a case of Nievergelt syndrome, a rare form of mesomelic dysplasia. Besides the characteristic mesomelic limb anomalies of Nievergelt syndrome, this patient exhibited two additional features: agenesis of the cerebellar vermis and cataracts, both of which have not been previously reported. (C) 2002 Wiley-Liss, Inc.
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.titlePatient with the mesomelic dysplasia, Nievergelt syndrome, and cerebellovermian agenesis and cataracts
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF MEDICAL GENETICS
dc.contributor.department, ,
dc.identifier.volume109
dc.identifier.issue3
dc.identifier.startpage206
dc.identifier.endpage210
dc.contributor.firstauthorID165040


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