1. The Marfan syndrome: diagnosis and management;Pyeritz, R.E.; McKusick, V.A.;N Engl J Med,1979
2. Clinical variability in the Marfan syndrome(s). Birth Defects defect in this condition. We propose that the two severely affected sibs represent examples of homozygosity for the Marfan gene. This assumption is based on the severe and;Pyeritz, R.E.; Murphy, E.A.; McKusick, V.A.,1979
3. Impaired conversion of procollagen to collagen by fibroblasts and bone treated with tunicamycin, an inhibitor of protein glycosylation;Duksin, D.; Bornstein, P.;JBiol Chem,1977
4. Relationship of the structure and biological activity of the natural homologues of tunicamycin;Duksin, D.; Mahoney, W.C.;J Biol Chem,1982
5. Basic defects in the Marfan syndrome;Pyeritz, R.E.; McKusick, V.A.;N Engl J Med,1981