Publications by authors named "Kenneth G Noble"

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A Thr17Met mutation is associated with an unusual retinochoroidopathy in an autosomal dominant pedigree.
Sherry J Bass, Kenneth G Noble

Retina· August 2008

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Autosomal dominant pericentral retinochoroidal atrophy.
Sherry J Bass, Kenneth G Noble

Retina· January 2006

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Choroideremia with polydactyly mimicking the Laurence-Moon-Bardet-Biedl syndrome.
Stephen G Schwartz, Kenneth G Noble, Ronald E Carr

Retina· June 2003

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