Works matching IS 09388990 AND DT 2002 AND VI 13 AND IP 1
Results: 11
Human O-GlcNAc transferase (OGT): genomic structure, analysis of splice variants, fine mapping in Xq13.1.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 62, doi. 10.1007/s00335-001-2108-9
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Characterization of a putative murine mitochondrial transporter homology of hMRS3/4.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 20, doi. 10.1007/s00335-001-2094-y
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Multiple blood pressure QTL on rat Chromosome 2 defined by congenic Dahl rats.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 41, doi. 10.1007/s00335-001-2114-y
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CAN—a pan-carnivore SINE family.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 50, doi. 10.1007/s00335-001-2111-1
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Mapping of an immotile short tail sperm defect in the Finnish Yorkshire on porcine Chromosome 16.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 45, doi. 10.1007/s00335-001-2104-0
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High-resolution mapping of the Gli3 mutation Extra-toes<sup>J</sup> reveals a 51.5-kb deletion.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 58, doi. 10.1007/s00335-001-2115-X
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Insertional mutation of the Attractin gene in the black tremor hamster.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 36, doi. 10.1007/s00335-001-2116-9
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Inheritance patterns of maternal alleles in imprinted regions of the mouse genome at different stages of development.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 24, doi. 10.1007/s00335-001-2095-x
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Genetic, physical, and comparative map of the subtelomeric region of mouse Chromosome 4.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 5, doi. 10.1007/s0033501-2109-8
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A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 30, doi. 10.1007/s00335-001-3038-2
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The origins of mouse genetics: beyond the Bussey Institution.II. Defining the problem of mouse supply: the 1928 National Research Council Committee on Experimental Plants and Animals.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 2, doi. 10.1007/s00335-001-4008-4
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