DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
LinksClose Window
References
De Falco F, Cainarca S, Andolfi G. , et al.
X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum.
Am J Med Genet A 2003;
120A (02) 222-228
Access:
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.