000 01245 a2200385 4500
005 20250515184954.0
264 0 _c20100618
008 201006s 0 0 eng d
022 _a1601-0825
024 7 _a10.1111/j.1601-0825.2009.01623.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRyoo, H-M
245 0 0 _aRUNX2 mutations in cleidocranial dysplasia patients.
_h[electronic resource]
260 _bOral diseases
_cJan 2010
300 _a55-60 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aChild
650 0 4 _aCleidocranial Dysplasia
_xcomplications
650 0 4 _aCodon, Nonsense
650 0 4 _aCore Binding Factor Alpha 1 Subunit
_xgenetics
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation, Missense
650 0 4 _aPedigree
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aTooth, Supernumerary
_xetiology
700 1 _aKang, H-Y
700 1 _aLee, S-K
700 1 _aLee, K-E
700 1 _aKim, J-W
773 0 _tOral diseases
_gvol. 16
_gno. 1
_gp. 55-60
856 4 0 _uhttps://doi.org/10.1111/j.1601-0825.2009.01623.x
_zAvailable from publisher's website
999 _c19142566
_d19142566