Cain, S. A., McGovern, A., Baldwin, A. K., Baldock, C., & Kielty, C. M. (2012). Fibrillin-1 Mutations Causing Weill-Marchesani Syndrome and Acromicric and Geleophysic Dysplasias Disrupt Heparan Sulfate Interactions. Public Library of Science.

Cain, Stuart A., Amanda McGovern, Andrew K. Baldwin, Clair Baldock, and Cay M. Kielty. Fibrillin-1 Mutations Causing Weill-Marchesani Syndrome and Acromicric and Geleophysic Dysplasias Disrupt Heparan Sulfate Interactions. Public Library of Science, 2012.

Cain, Stuart A., et al. Fibrillin-1 Mutations Causing Weill-Marchesani Syndrome and Acromicric and Geleophysic Dysplasias Disrupt Heparan Sulfate Interactions. Public Library of Science, 2012.