RUNX2 analysis of Danish cleidocranial dysplasia families

Keyphrases

• Runt-related Transcription Factor 2 (Runx2) 100%
• Cleidocranial Dysplasia 100%
• Genotype 16%
• Polymorphism 16%
• Autosomal Dominant 16%
• Missense mutation 16%
• In(III) 16%
• Promoter Region 16%
• Mutation Analysis 16%
• Nonsense mutation 16%
• Phenotypic Variation 16%
• Large Deletion 16%
• Pathogenic mutations 16%
• Chromosomal Aberrations 16%
• Frameshift mutation 16%
• Runt 16%
• Polyalanine Repeat 16%
• Polyglutamine 16%
• Copy number Analysis 16%
• RUNX2 mutation 16%
• Inherited Disease 16%
• Large Duplication 16%

Biochemistry, Genetics and Molecular Biology

• Dysplasia 100%
• RUNX2 100%
• Autosomal Dominant Inheritance 14%
• Promoter Region 14%
• Missense Mutation 14%
• Nonsense Mutation 14%
• Genetic Disorder 14%
• Copy Number Analysis 14%