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  A novel 18-bp in-frame deletion mutation in RUNX2 causes cleidocranial dysplasia
 
 
Title: A novel 18-bp in-frame deletion mutation in RUNX2 causes cleidocranial dysplasia
Author: Zeng, Li
Wei, Jiahui
Zhao, Na
Sun, Shichen
Wang, Yixiang
Feng, Hailan
Appeared in: Archives of oral biology
Paging: Volume 96 (2018) nr. C pages 243-248
Year: 2018
Contents:
Publisher: Elsevier Ltd
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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