DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
LinksClose Window
References
Wimplinger I, Shaw GM, Kutsche K.
HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations?.
Mol Vis 2007;
13: 1475-1482
Access:
We do not assume any responsibility for the contents of the web pages of other providers.