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J L Wiggs

Showing results (21-30 of 32) with videos related to

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American Journal of Human Genetics|April 27, 2004
A genomewide scan identifies novel early-onset primary open-angle glaucoma loci on 9q22 and 20p12J L Wiggs, S Lynch, G Ynagi, et al.
American Journal of Human Genetics|September 1, 1996
A second locus for Rieger syndrome maps to chromosome 13q14J C Phillips, E A del Bono, J L Haines, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 1, 1997
A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36J S Andersen, A M Pralea, E A DelBono, et al.
Human Molecular Genetics|April 18, 2000
Genome-wide scan for adult onset primary open angle glaucomaJ L Wiggs, R R Allingham, A Hossain, et al.
Clinical Genetics|April 30, 2013
Variations in COL15A1 and COL18A1 influence age of onset of primary open angle glaucomaJ L Wiggs, G R Howell, K Linkroum, et al.
Molecular Vision|December 9, 2010
Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thicknessT Desronvil, D Logan-Wyatt, W Abdrabou, et al.
Human Heredity|September 28, 1998
Adult-onset primary open angle glaucoma does not localize to chromosome 2cen-q13 in North American familiesR R Allingham, J L Wiggs, K F Damji, et al.
American Journal of Human Genetics|October 30, 1998
Prevalence of mutations in TIGR/Myocilin in patients with adult and juvenile primary open-angle glaucomaJ L Wiggs, R R Allingham, D Vollrath, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Gln368STOP myocilin mutation in families with late-onset primary open-angle glaucomaR R Allingham, J L Wiggs, M A De La Paz, et al.
Eye (London, England)|January 14, 2017
Nailfold capillary morphology in exfoliation syndromeC C Cousins, J H Kang, C Bovee, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|April 27, 2004
A genomewide scan identifies novel early-onset primary open-angle glaucoma loci on 9q22 and 20p12J L Wiggs, S Lynch, G Ynagi, et al.
American Journal of Human Genetics|September 1, 1996
A second locus for Rieger syndrome maps to chromosome 13q14J C Phillips, E A del Bono, J L Haines, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 1, 1997
A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36J S Andersen, A M Pralea, E A DelBono, et al.
Human Molecular Genetics|April 18, 2000
Genome-wide scan for adult onset primary open angle glaucomaJ L Wiggs, R R Allingham, A Hossain, et al.
Clinical Genetics|April 30, 2013
Variations in COL15A1 and COL18A1 influence age of onset of primary open angle glaucomaJ L Wiggs, G R Howell, K Linkroum, et al.
Molecular Vision|December 9, 2010
Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thicknessT Desronvil, D Logan-Wyatt, W Abdrabou, et al.
Human Heredity|September 28, 1998
Adult-onset primary open angle glaucoma does not localize to chromosome 2cen-q13 in North American familiesR R Allingham, J L Wiggs, K F Damji, et al.
American Journal of Human Genetics|October 30, 1998
Prevalence of mutations in TIGR/Myocilin in patients with adult and juvenile primary open-angle glaucomaJ L Wiggs, R R Allingham, D Vollrath, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Gln368STOP myocilin mutation in families with late-onset primary open-angle glaucomaR R Allingham, J L Wiggs, M A De La Paz, et al.
Eye (London, England)|January 14, 2017
Nailfold capillary morphology in exfoliation syndromeC C Cousins, J H Kang, C Bovee, et al.
Pageof 4