000 01260 a2200361 4500
005 20250517133804.0
264 0 _c20170313
008 201703s 0 0 eng d
022 _a2542-5641
024 7 _a10.4103/0366-6999.197996
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aQin, Xue-Yan
245 0 0 _aNovel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case.
_h[electronic resource]
260 _bChinese medical journal
_c01 2017
300 _a165-170 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdolescent
650 0 4 _aCell Nucleus
_xmetabolism
650 0 4 _aCleidocranial Dysplasia
_xgenetics
650 0 4 _aCore Binding Factor Alpha 1 Subunit
_xgenetics
650 0 4 _aFemale
650 0 4 _aFrameshift Mutation
_xgenetics
650 0 4 _aHumans
650 0 4 _aMicroscopy, Fluorescence
650 0 4 _aMutation
700 1 _aJia, Pei-Zeng
700 1 _aZhao, Hua-Xiang
700 1 _aLi, Wei-Ran
700 1 _aChen, Feng
700 1 _aLin, Jiu-Xiang
773 0 _tChinese medical journal
_gvol. 130
_gno. 2
_gp. 165-170
856 4 0 _uhttps://doi.org/10.4103/0366-6999.197996
_zAvailable from publisher's website
999 _c26788178
_d26788178