Publisher： Karger
E-ISSN： 1661-8777|8|5|253-260
ISSN： 1661-8769
Source： Molecular Syndromology, Vol.8, Iss.5, 2017-06, pp. : 253-260
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Related content
A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia
Molecular Syndromology, Vol. 6, Iss. 1, 2015-01 ,pp. :
Access to resources
Recommend
A Runx2 threshold for the cleidocranial dysplasia phenotype
By Lou Yang Javed Amjad Hussain Sadiq Colby Jennifer Frederick Dana Pratap Jitesh Xie Ronglin Gaur Tripti van Wijnen Andre J. Jones Stephen N. Stein Gary S. Lian Jane B. Stein Janet L.
Human Molecular Genetics, Vol. 18, Iss. 3, 2009-02 ,pp. :
By Zhou Guang Chen Yuqing Zhou Lei Thirunavukkarasu Kannan Hecht Jacqueline
Human Molecular Genetics, Vol. 8, Iss. 12, 1999-11 ,pp. :
A Novel Nonsense Mutation of the Sedlin Gene in a Family with Spondyloepiphyseal Dysplasia Tarda
Human Heredity, Vol. 54, Iss. 1, 2002-11 ,pp. :