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

Autor Sena, D, Finzi, S, Rodgers, K, Del Bono, E, Haines, J, Wiggs, J
Vydáno 2004

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

Autor Sud, A., Del Bono, E.A., Haines, J.L., Wiggs, J.L.
Vydáno 2008

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

Autor Paglinauan, C, Haines, J L, Del Bono, E A, Schuman, J, Stawski, S, Wiggs, J L
Vydáno 1995

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

Autor Wiggs, J. L., Lynch, S., Ynagi, G., Maselli, M., Auguste, J., Del Bono, E. A., Olson, L. M., Haines, J. L.
Vydáno 2004

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

Autor Phillips, J. C., del Bono, E. A., Haines, J. L., Pralea, A. M., Cohen, J. S., Greff, L. J., Wiggs, J. L.
Vydáno 1996

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

Autor 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.
Vydáno 2010

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

Autor 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
Vydáno 1998