DOI:
10.1055/s-00000085
The Thoracic and Cardiovascular Surgeon
LinksClose Window
References
Milewicz DM, Grossfield J, Cao SN, Kielty C, Covitz W, Jewett T.
A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features of the Marfan syndrome.
J Clin Invest 1995;
95 (05) 2373-2378
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.