Founder mutations of CYP1B1 gene in patients with congenital glaucoma from the United States and Brazil

Por Sena, D, Finzi, S, Rodgers, K, Del Bono, E, Haines, J, Wiggs, J
Publicado em 2004

Fine mapping of the GLC1K juvenile primary open-angle glaucoma locus and exclusion of candidate genes

Por Sud, A., Del Bono, E.A., Haines, J.L., Wiggs, J.L.
Publicado em 2008

Exclusion of chromosome 1q21-q31 from linkage to three pedigrees affected by the pigment-dispersion syndrome.

Por Paglinauan, C, Haines, J L, Del Bono, E A, Schuman, J, Stawski, S, Wiggs, J L
Publicado em 1995

A Genomewide Scan Identifies Novel Early-Onset Primary Open-Angle Glaucoma Loci on 9q22 and 20p12

Por Wiggs, J. L., Lynch, S., Ynagi, G., Maselli, M., Auguste, J., Del Bono, E. A., Olson, L. M., Haines, J. L.
Publicado em 2004

A second locus for Rieger syndrome maps to chromosome 13q14.

Por Phillips, J. C., del Bono, E. A., Haines, J. L., Pralea, A. M., Cohen, J. S., Greff, L. J., Wiggs, J. L.
Publicado em 1996

Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thickness

Por Desronvil, T., Logan-Wyatt, D., Abdrabou, W., Triana, M., Jones, R., Taheri, S., Del Bono, E., Pasquale, L.R., Olivier, M., Haines, J.L., Fan, B.J., Wiggs, J.L.
Publicado em 2010

Prevalence of mutations in TIGR/Myocilin in patients with adult and juvenile primary open-angle glaucoma.

Por Wiggs, J L, Allingham, R R, Vollrath, D, Jones, K H, De La Paz, M, Kern, J, Patterson, K, Babb, V L, Del Bono, E A, Broomer, B W, Pericak-Vance, M A, Haines, J L
Publicado em 1998