Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.

Jaruga, A

Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation. [electronic resource] - Clinical genetics 11 2016 - 393-402 p. digital

Publication Type: Journal Article; Review; Research Support, Non-U.S. Gov't

1399-0004

10.1111/cge.12812 doi


Cleidocranial Dysplasia--genetics
Core Binding Factor Alpha 1 Subunit--genetics
Genetic Association Studies
Heterozygote
Humans
Mutation
Pedigree
Phenotype