has been cited by the following article(s):
|
[1]
|
Identification of a Novel Splice Site Mutation in RUNX2 Gene in a Family with Rare Autosomal Dominant Cleidocranial Dysplasia
Iranian Biomedical Journal,
2021
DOI:10.52547/ibj.25.4.297
|
|
|
|
|
[2]
|
Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family
Clinical Case Reports,
2020
DOI:10.1002/ccr3.2825
|
|
|
|
|
[3]
|
Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia
Archives of Oral Biology,
2019
DOI:10.1016/j.archoralbio.2019.02.005
|
|
|
|