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Citation: Am. Mallon et al., Comparative genome sequence analysis of the Bpa/Str region in mouse and man, GENOME RES, 10(6), 2000, pp. 758-775
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Citation: Am. Isaacs et al., Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy, HUM MOL GEN, 9(12), 2000, pp. 1865-1871
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Citation: Xz. Liu et al., Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss, HUM MOL GEN, 9(1), 2000, pp. 63-67
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Citation: Pm. Nolan et al., Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource, MAMM GENOME, 11(7), 2000, pp. 500-506
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Citation: Ma. Strivens et al., Informatics for mutagenesis: the design of Mutabase - a distributed data recording system for animal husbandry, mutagenesis, and phenotypic analysis, MAMM GENOME, 11(7), 2000, pp. 577-583
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Citation: Ajw. Paige et al., A deletion on Chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate, MAMM GENOME, 11(1), 2000, pp. 51-57
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Citation: Ae. Kiernan et al., Several new mouse mutations affect semicircular canal morphogenesis of theinner ear, BR J AUDIOL, 34(2), 2000, pp. 85-86
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Citation: A. Erven et al., Phenotypic analysis of new deaf and vestibular mouse mutants, BR J AUDIOL, 34(2), 2000, pp. 85-85