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Temporal aspects in craniometaphyseal dysplasia: Autosomal recessive type

dc.contributor.authorElcioglu, N
dc.contributor.authorHall, CM
dc.date.accessioned2021-03-04T17:35:42Z
dc.date.available2021-03-04T17:35:42Z
dc.date.issued1998
dc.identifier.citationElcioglu N., Hall C., "Temporal aspects in craniometaphyseal dysplasia: Autosomal recessive type", AMERICAN JOURNAL OF MEDICAL GENETICS, cilt.76, sa.3, ss.245-251, 1998
dc.identifier.issn0148-7299
dc.identifier.otherav_86602e42-eaee-4bfc-b6a4-3055cbc71c3f
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/91312
dc.description.abstractWe present the clinical and radiographic findings in a patient with the autosomal recessive form of craniometaphyseal dysplasia (CMD). The changes from infancy to the age of 17 years are illustrated and discussed. (C) 1998 Wiley-Liss, Inc.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.titleTemporal aspects in craniometaphyseal dysplasia: Autosomal recessive type
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF MEDICAL GENETICS
dc.contributor.department, ,
dc.identifier.volume76
dc.identifier.issue3
dc.identifier.startpage245
dc.identifier.endpage251
dc.contributor.firstauthorID120620


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