DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
LinksClose Window
References
Carta C, Pantaleoni F, Bocchinfuso G. , et al.
Germline missense mutations affecting KRAS isoform B are associated with a severe Noonan syndrome phenotype.
Am J Hum Genet 2006;
79 (01) 129-135
We do not assume any responsibility for the contents of the web pages of other providers.