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Human Molecular Genetics 1
Showing records 1 to 1 | Display all abstracts in Human Molecular Genetics5552 Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus
Bejjani BA; Stockton DW; Lewis RA; Tomey KF
Human Molecular Genetics 2000; 9:367-374
