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Showing results (21-30 of 24) with videos related to

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The American Journal of Physiology|June 11, 1999
Molecular mechanism underlying a Cx50-linked congenital cataractJ D Pal, V M Berthoud, E C Beyer, et al.
American Journal of Physiology. Cell Physiology|August 16, 2000
Connexin46 mutations linked to congenital cataract show loss of gap junction channel functionJ D Pal, X Liu, D Mackay, et al.
Journal of Medical Genetics|November 17, 2007
A novel connexin50 mutation associated with congenital nuclear pulverulent cataractsA Arora, P J Minogue, X Liu, et al.
Journal of Medical Genetics|January 7, 2006
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataractA Arora, P J Minogue, X Liu, et al.
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Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
The American Journal of Physiology|June 11, 1999
Molecular mechanism underlying a Cx50-linked congenital cataractJ D Pal, V M Berthoud, E C Beyer, et al.
American Journal of Physiology. Cell Physiology|August 16, 2000
Connexin46 mutations linked to congenital cataract show loss of gap junction channel functionJ D Pal, X Liu, D Mackay, et al.
Journal of Medical Genetics|November 17, 2007
A novel connexin50 mutation associated with congenital nuclear pulverulent cataractsA Arora, P J Minogue, X Liu, et al.
Journal of Medical Genetics|January 7, 2006
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataractA Arora, P J Minogue, X Liu, et al.
Pageof 3