Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2006-10-30
pubmed:abstractText
Cleidocranial dysplasia (CCD) is a rare dysplasia of bony and dental tissue. Characteristic are typical craniofacial and dental findings including morphological anomalies. CCD is possibly the only general syndrome that can be diagnosed based on the dental findings alone. CCD correlates with mutations in the RUNX2 gene.
pubmed:language
ger
pubmed:journal
pubmed:citationSubset
D
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1432-9417
pubmed:author
pubmed:issnType
Print
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
385-93
pubmed:meshHeading
pubmed-meshheading:17051365-Adolescent, pubmed-meshheading:17051365-Adult, pubmed-meshheading:17051365-Alternative Splicing, pubmed-meshheading:17051365-Child, pubmed-meshheading:17051365-Chromosomes, Human, Pair 6, pubmed-meshheading:17051365-Cleidocranial Dysplasia, pubmed-meshheading:17051365-Cohort Studies, pubmed-meshheading:17051365-Core Binding Factor Alpha 1 Subunit, pubmed-meshheading:17051365-DNA Mutational Analysis, pubmed-meshheading:17051365-Exons, pubmed-meshheading:17051365-Facies, pubmed-meshheading:17051365-Female, pubmed-meshheading:17051365-Humans, pubmed-meshheading:17051365-Male, pubmed-meshheading:17051365-Middle Aged, pubmed-meshheading:17051365-Mutation, Missense, pubmed-meshheading:17051365-Phenotype, pubmed-meshheading:17051365-Radiography, Panoramic, pubmed-meshheading:17051365-Tomography, X-Ray Computed, pubmed-meshheading:17051365-Tooth Abnormalities
pubmed:year
2006
pubmed:articleTitle
[Cleidocranial dysplasia. Description and analysis of a patient cohort].
pubmed:affiliation
AG Kraniofaziale Genetik/Tissue Engineering, BioPark Regensburg, Zentrum für Medizinische Biotechnologie, Josef-Engert-Strasse 9, 93051 Regensburg, Germany. uwe.baumert@klinik.uni-regensburg.de
pubmed:publicationType
Journal Article, English Abstract