In frame fibrillin-1 gene deletion in autosomal dominant Weill­Marchesani syndrome.
Faivere, L.; Gorlin, R. J.; Wirtz, M. K.; Godfrey, M.; Dagoneau, N.; Samples, J. R.; Le Merrer, M.; Collod-Beroud, G.; Boileau, C.; Munnich, A.; Cormier-Daire, V.; Journal of Medical Genetics, 2003, vol. 40, issue 1, p 34, ISSN 00222593. ISBN 14686244.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef