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Genomic, transcriptional and mutational analysis of the mouse microphthalmia locus.
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Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF.
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Characterization and repeat analysis of the compact genome of the freshwater pufferfish Tetraodon nigroviridis.
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The evolutionary fate and consequences of duplicate genes.
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Zebrafish comparative genomics and the origins of vertebrate chromosomes.
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An L1 element intronic insertion in the black-eyed white (Mitf[mi-bw]) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness.
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