In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome: Figure 1Laurence Faivre, Valérie Cormier‐Daire, Robert J. Gorlin et al.|Journal of Medical Genetics|2003Cited by 281
Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q.Mary K. Wirtz, Ted S. Acott, J. R. Samples et al.|PubMed|1997Cited by 212
Variants in ASB10 are associated with open-angle glaucomaFrancesca Pasutto, Mary K. Wirtz, Kate E. Keller et al.|Human Molecular Genetics|2011Cited by 82
Weill-Marchesani syndrome - possible linkage of the autosomal dominant form to 15q21.1Mary K. Wirtz, Maurice Godfrey, J. R. Samples et al.|American Journal of Medical Genetics|1996Cited by 48
Regulation of ABC Transporters and Glaucoma: New IdeasPaul A. Knepper, Jianbo Yue, M. J. Nolan et al.|Unknown|2006Cited by 2