Publisher: Karger
E-ISSN: 1661-8777|3|4|158-168
ISSN: 1661-8769
Source: Molecular Syndromology, Vol.3, Iss.4, 2012-09, pp. : 158-168
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
SOX2 anophthalmia syndrome and dental anomalies
American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. :
Genes Involved in Hereditary Hearing Impairment
Current Genomics, Vol. 4, Iss. 5, 2003-07 ,pp. :