(Q52171299)
Statements
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Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. (English)
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B A Bejjani
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D W Stockton
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R A Lewis
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K F Tomey
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D K Dueker
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M Jabak
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W F Astle
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J R Lupski
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1 February 2000
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9
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367-374
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3
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Identifiers
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1 reference