Works matching IS 09646906 AND DT 2005 AND VI 14 AND IP suppl_2
Results: 17
Susceptibility genes for complex epilepsy.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R243, doi. 10.1093/hmg/ddi355
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- Article
Interactome: gateway into systems biology.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R171, doi. 10.1093/hmg/ddi335
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- Article
Synapse proteomics of multiprotein complexes: en route from genes to nervous system diseases.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R225, doi. 10.1093/hmg/ddi330
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- Article
Gearing up for genome-wide gene-association studies.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R157, doi. 10.1093/hmg/ddi273
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- Article
Insights into X-linked retinitis pigmentosa type 3, allied diseases and underlying pathomechanisms.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R259, doi. 10.1093/hmg/ddi272
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- Article
Camels and zebrafish, viruses and cancer: a microRNA update.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R183, doi. 10.1093/hmg/ddi271
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- Article
Emerging functions of mammalian mitochondrial fusion and fission.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R283, doi. 10.1093/hmg/ddi270
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- Article
Small molecule intervention in microtubule-associated human disease.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R291, doi. 10.1093/hmg/ddi269
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- Article
Identification of disease genes by whole genome CGH arrays.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R215, doi. 10.1093/hmg/ddi268
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- Article
Genetical genomics: combining genetics with gene expression analysis.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R163, doi. 10.1093/hmg/ddi267
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- Article
The first molecular details of ALT in human tumor cells.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R191, doi. 10.1093/hmg/ddi266
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- Article
Mechanisms of common fragile site instability.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R197, doi. 10.1093/hmg/ddi265
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- Article
Genetic basis of Joubert syndrome and related disorders of cerebellar development.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R235, doi. 10.1093/hmg/ddi264
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- Article
The genetics of attention deficit hyperactivity disorder.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R275, doi. 10.1093/hmg/ddi263
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- Article
The genetics of Fraser syndrome and the blebs mouse mutants.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R269, doi. 10.1093/hmg/ddi262
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- Article
Pharmacogenetics/genomics and personalized medicine.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R207
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- Article
Tuberous sclerosis: a GAP at the crossroads of multiple signaling pathways.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R251, doi. 10.1093/hmg/ddi260
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- Article