Showing results (1-10 of 7) with videos related to
Sort By:
Pageof 1
Clinical Genetics|September 1, 1996
X-linked exudative vitreoretinopathy caused by an arginine to leucine substitution (R121L) in the Norrie disease proteinK Johnson, H A Mintz-Hittner, Y P Conley, et al.Placenta|August 10, 2010
LAIR2 localizes specifically to sites of extravillous trophoblast invasionS A Founds, B Fallert-Junecko, T A Reinhart, et al.Placenta|November 26, 2008
Altered global gene expression in first trimester placentas of women destined to develop preeclampsiaS A Founds, Y P Conley, J F Lyons-Weiler, et al.Molecular Genetics and Metabolism|January 4, 2001
Three novel activating mutations in the calcium-sensing receptor responsible for autosomal dominant hypocalcemiaY P Conley, D N Finegold, D G Peters, et al.Human Molecular Genetics|May 18, 2000
A full genome scan for age-related maculopathyD E Weeks, Y P Conley, T S Mah, et al.American Journal of Human Genetics|March 23, 2000
A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2Y P Conley, D Erturk, A Keverline, et al.American Journal of Ophthalmology|November 13, 2001
Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regionsD E Weeks, Y P Conley, H J Tsai, et al.Pageof 1