Works matching IS 09646906 AND DT 2004 AND VI 13 AND IP suppl_1
Results: 19
Gain-of-function polymorphism in mouse and human Ltk: implications for the pathogenesis of systemic lupus erythematosus.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. 171, doi. 10.1093/hmg/ddh020
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Genetics of inflammatory bowel disease: progress and prospects.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R161
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Genetics of essential hypertension.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R169
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Alzheimer's disease: one disorder, too many genes?
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R135
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The genetics of psoriasis, psoriatic arthritis and atopic dermatitis.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R43
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The law of mass action applied to neurodegenerative disease: a hypothesis concerning the etiology and pathogenesis of complex diseases.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R123
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Quantitative genetic variation: a post-modern view.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R1
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The oligogenic properties of Bardet–Biedl syndrome.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R65
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Parkin genetics: one model for Parkinson's disease.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R127
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Asthma genetics 2003.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R83
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The genetic basis of systemic lupus erythematosus—knowledge of today and thoughts for tomorrow.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R143
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Patterns of ethnic diversity among the genes that influence AIDS.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R9
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Genetic dissection of myocilin glaucoma.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R91
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Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R57
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The complex genetic epidemiology of prostate cancer.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R103
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Genetics of familial combined hyperlipidemia and risk of coronary heart disease.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R149, doi. 10.1093/hmg/ddh069
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Type 2 diabetes mellitus: not quite exciting enough?
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R21
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Progress in defining the molecular basis of type 2 diabetes mellitus through susceptibility-gene identification.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R33
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Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R73
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