Two novel mutations and a neutral polymorphism in EGF-like domains of the fibrillin gene (FBN1): SSCP screening of exons 15–21 in Marfan syndrome patients

Abstract
Caroline Hayward, Alison L. Rae, Mary E.M. Porteous, Lindsay J. Logie, David J.H. Brock; Two novel mutations and a neutral polymorphism in EGF-like domains of