Milewicz D.M.,1995


Milewicz D.M., Grossfield J., Cao S.N., 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, v. 95, p. 2373-2378.

Смотрите также:

  • Табл. FBN m