Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype–phenotype correlations

2003 ◽  
Vol 30 (2) ◽  
pp. 184-193 ◽  
Author(s):  
Taketoshi Yoshida ◽  
Hirokazu Kanegane ◽  
Motomi Osato ◽  
Masatoshi Yanagida ◽  
Toshio Miyawaki ◽  
...  
Keyword(s):  
Functional Analysis ◽  
Cleidocranial Dysplasia

Author response for "Functional analysis of novel RUNX2 mutations identified in patients with Cleidocranial dysplasia"

2019 ◽  
Author(s):  
Ewa Hordyjewska‐Kowalczyk ◽  
Anna SowiŃska‐Seidler ◽  
Ewelina M. Olech ◽  
Magdalena Socha ◽  
Renata Glazar ◽  
...  
Keyword(s):  
Functional Analysis ◽  
Author Response ◽  
Cleidocranial Dysplasia

scholarly journals Functional Analysis of RUNX2 Mutations in Japanese Patients with Cleidocranial Dysplasia Demonstrates Novel Genotype-Phenotype Correlations

2002 ◽  
Vol 71 (4) ◽  
pp. 724-738 ◽  
Author(s):  
Taketoshi Yoshida ◽  
Hirokazu Kanegane ◽  
Motomi Osato ◽  
Masatoshi Yanagida ◽  
Toshio Miyawaki ◽  
...  
Keyword(s):  
Functional Analysis ◽  
Japanese Patients ◽  
Cleidocranial Dysplasia ◽  
Novel Genotype

scholarly journals Functional analysis of novel RUNX2 mutations in cleidocranial dysplasia

Mutagenesis ◽  
2017 ◽  
Vol 32 (4) ◽  
pp. 437-443 ◽  
Author(s):  
Li Zeng ◽  
Jiahui Wei ◽  
Dong Han ◽  
Haochen Liu ◽  
Yang Liu ◽  
...  
Keyword(s):  
Functional Analysis ◽  
Cleidocranial Dysplasia

Author response for "Functional analysis of novel RUNX2 mutations identified in patients with Cleidocranial dysplasia"

2019 ◽  
Author(s):  
Ewa Hordyjewska‐Kowalczyk ◽  
Anna SowiŃska‐Seidler ◽  
Ewelina M. Olech ◽  
Magdalena Socha ◽  
Renata Glazar ◽  
...  
Keyword(s):  
Functional Analysis ◽  
Author Response ◽  
Cleidocranial Dysplasia

scholarly journals Functional analysis of a novel RUNX2 missense mutation found in a family with cleidocranial dysplasia

2005 ◽  
Vol 50 (12) ◽  
pp. 679-683 ◽  
Author(s):  
Cinzia Puppin ◽  
Lucia Pellizzari ◽  
Dora Fabbro ◽  
Federico Fogolari ◽  
Gianluca Tell ◽  
...  
Keyword(s):  
Functional Analysis ◽  
Missense Mutation ◽  
Cleidocranial Dysplasia
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