![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
Publisher: Karger
E-ISSN: 1661-8777|2|1|21-26
ISSN: 1661-8769
Source: Molecular Syndromology, Vol.2, Iss.1, 2011-10, pp. : 21-26
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
![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. :
![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
COL2A1 Mutation in Spondylometaphyseal Dysplasia Algerian Type
Molecular Syndromology, Vol. 4, Iss. 3, 2013-01 ,pp. :
![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
COL9A2 and COL9A3 mutations in canine autosomal recessive oculoskeletal dysplasia
Mammalian Genome, Vol. 21, Iss. 7-8, 2010-08 ,pp. :