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Mutations in the Human Sterol Δ7-Reductase Gene at 11q12-13 Cause Smith-Lemli-Opitz Syndrome
Download from doi.orgLhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development
Download from journals.biologists.comMolecular analysis of a metalloprotease from Proteus mirabilis.
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