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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 1, 2024. (Total: 233962Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Leber Congenital Amaurosis and RDS[original query]
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.
Human mutation 2001 1 17 (1): 42-51.
Sohocki M M, Daiger S P, Bowne S J, Rodriquez J A, Northrup H, Heckenlively J R, Birch D G, Mintz-Hittner H, Ruiz R S, Lewis R A, Saperstein D A, Sullivan L
Utility of molecular testing for related retinal dystrophies.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie 2006 Apr 41 (2): 190-6.
Mezer Eedy, Sutherland Joanne, Goei Stephanie L, Héon Elise, Levin Alex
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