Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case.

Qin, Xue-Yan

Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case. [electronic resource] - Chinese medical journal 01 2017 - 165-170 p. digital

Publication Type: Case Reports; Journal Article

2542-5641

10.4103/0366-6999.197996 doi


Adolescent
Cell Nucleus--metabolism
Cleidocranial Dysplasia--genetics
Core Binding Factor Alpha 1 Subunit--genetics
Female
Frameshift Mutation--genetics
Humans
Microscopy, Fluorescence
Mutation