TY  - GEN
AU  - Ryoo,H-M
AU  - Kang,H-Y
AU  - Lee,S-K
AU  - Lee,K-E
AU  - Kim,J-W
TI  - RUNX2 mutations in cleidocranial dysplasia patients
SN  - 1601-0825
PY  - 2010///0618
KW  - Child
KW  - Cleidocranial Dysplasia
KW  - complications
KW  - Codon, Nonsense
KW  - Core Binding Factor Alpha 1 Subunit
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Female
KW  - Humans
KW  - Male
KW  - Mutation, Missense
KW  - Pedigree
KW  - Polymorphism, Single Nucleotide
KW  - Tooth, Supernumerary
KW  - etiology
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1601-0825.2009.01623.x
ER  -