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A Mutation in Af4 Is Predicted to Cause Cerebellar Ataxia and Cataracts in the Robotic Mouse.
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- Journal of Neuroscience, 2003, v. 23, n. 5, p. 1631, doi. 10.1523/JNEUROSCI.23-05-01631.2003
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- Article
Characterization of Common Genetic Variants in Cathepsin K and Testing for Association With Bone Mineral Density in a Large Cohort of Perimenopausal Women From Scotland.
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- Journal of Bone & Mineral Research, 2004, v. 19, n. 1, p. 31, doi. 10.1359/jbmr.0301205
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- Article
Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland.
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- Nature Genetics, 2001, v. 28, n. 2, p. 128, doi. 10.1038/88839
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- Article
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.
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- Nature Genetics, 2000, v. 25, n. 4, p. 440, doi. 10.1038/78140
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- Article
CCR2 and coronary artery disease: a woscopssubstudy.
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- BMC Research Notes, 2010, v. 3, p. 31, doi. 10.1186/1756-0500-3-31
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- Article
Novel phenotypes identified by plasma biochemical screening in the mouse.
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- Mammalian Genome, 2002, v. 13, n. 10, p. 595, doi. 10.1007/s00335-002-2188-1
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- Article
Single nucleotide polymorphisms as tools in human genetics.
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- Human Molecular Genetics, 2000, v. 9, n. 16, doi. 10.1093/hmg/9.16.2403
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- Article
Silicon Analogues of the Nonpeptidic GnRH Antagonist AG-045572: Syntheses, Crystal Structure Analyses, and Pharmacological Characterization.
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- ChemMedChem, 2011, v. 6, n. 11, p. 2070, doi. 10.1002/cmdc.201100318
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- Article