Abstract This research resulted in the identification and submission of a novel RUNX2 gene mutation in the affected members of the studied pedigree. Mutation screening is an effective method for the early diagnosis of CCD in the affected individuals
Background: Cleidocranial dysplasia (CCD) is an autosomal dominant disease that affects the skeletal...
Abstract. Cleidocranial dysplasia (CCD) is an autosomal dominant inheritable skeletal disease caused...
Cleidocranial dysplasia (CCD) is a dominantly inherited skeletal dysplasia caused by mutations in th...
Cleidocranial dysplasia (CCD) is a dominantly inherited skeletal dysplasia caused by mutations in th...
Cleidocranial Dysplasia (CCD) is an autosomal dominant skeletal disorder characterized by hypoplasti...
Cleidocranial Dysplasia (CCD) is an autosomal dominant skeletal disorder characterized by hypoplasti...
Cleidocranial dysplasia (CCD) is a dominantly inherited skeletal dysplasia caused by mutations in th...
Cleidocranial Dysplasia (CCD) is an autosomal dominant skeletal disorder characterized by hypoplasti...
Cleidocranial dysplasia (CCD) is a autosomal dominant disorder characterized by skeletal anomalies s...
Cleidocranial Dysplasia (CCD) is an autosomal dominant skeletal disorder characterized by hypoplasti...
This study reports a novel identical complex disease allele harboring two non-synonymous mutations t...
Cleidocranial dysplasia (CCD) is an autosomal dominant inheritable skeletal disorder characterized b...
Cleidocranial dysplasia (CCD) is a congenital autosomal dominant syndrome characterised by dental an...
Background Cleidocranial dysplasia (CCD, #MIM119600) is an autosomal-dominant skeletal dysplasia cha...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disorder caused by mutation of r...
Background: Cleidocranial dysplasia (CCD) is an autosomal dominant disease that affects the skeletal...
Abstract. Cleidocranial dysplasia (CCD) is an autosomal dominant inheritable skeletal disease caused...
Cleidocranial dysplasia (CCD) is a dominantly inherited skeletal dysplasia caused by mutations in th...
Cleidocranial dysplasia (CCD) is a dominantly inherited skeletal dysplasia caused by mutations in th...
Cleidocranial Dysplasia (CCD) is an autosomal dominant skeletal disorder characterized by hypoplasti...
Cleidocranial Dysplasia (CCD) is an autosomal dominant skeletal disorder characterized by hypoplasti...
Cleidocranial dysplasia (CCD) is a dominantly inherited skeletal dysplasia caused by mutations in th...
Cleidocranial Dysplasia (CCD) is an autosomal dominant skeletal disorder characterized by hypoplasti...
Cleidocranial dysplasia (CCD) is a autosomal dominant disorder characterized by skeletal anomalies s...
Cleidocranial Dysplasia (CCD) is an autosomal dominant skeletal disorder characterized by hypoplasti...
This study reports a novel identical complex disease allele harboring two non-synonymous mutations t...
Cleidocranial dysplasia (CCD) is an autosomal dominant inheritable skeletal disorder characterized b...
Cleidocranial dysplasia (CCD) is a congenital autosomal dominant syndrome characterised by dental an...
Background Cleidocranial dysplasia (CCD, #MIM119600) is an autosomal-dominant skeletal dysplasia cha...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disorder caused by mutation of r...
Background: Cleidocranial dysplasia (CCD) is an autosomal dominant disease that affects the skeletal...
Abstract. Cleidocranial dysplasia (CCD) is an autosomal dominant inheritable skeletal disease caused...
Cleidocranial dysplasia (CCD) is a dominantly inherited skeletal dysplasia caused by mutations in th...
DOI
Add to ORKG