Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP suppl_2
Results: 22
Mitochondrial DNA polymerase-γ and human disease.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R244, doi. 10.1093/hmg/ddl233
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- Article
The genetic architecture of normal variation in human pigmentation: an evolutionary perspective and model.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R176, doi. 10.1093/hmg/ddl217
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- Article
Planar cell polarity, ciliogenesis and neural tube defects.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R227, doi. 10.1093/hmg/ddl216
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- Article
Genetics of obesity and the prediction of risk for health.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R124, doi. 10.1093/hmg/ddl215
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- Article
Molecular bases of progeroid syndromes.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R151, doi. 10.1093/hmg/ddl214
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- Article
Epigenetics of autism spectrum disorders.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R138, doi. 10.1093/hmg/ddl213
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- Article
Molecular components of the mammalian circadian clock.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R271, doi. 10.1093/hmg/ddl207
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- Article
Usher syndrome: molecular links of pathogenesis, proteins and pathways.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R262, doi. 10.1093/hmg/ddl205
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- Article
Recent advances in the genetics of amyotrophic lateral sclerosis and frontotemporal dementia: common pathways in neurodegenerative disease.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R182, doi. 10.1093/hmg/ddl202
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- Article
How lifetimes shape epigenotype within and across generations.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R131, doi. 10.1093/hmg/ddl200
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- Article
Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R220, doi. 10.1093/hmg/ddl197
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- Article
The many facets of the Wilms' tumour gene, WT1.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R196, doi. 10.1093/hmg/ddl196
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- Article
Towards understanding CRUMBS function in retinal dystrophies.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R235, doi. 10.1093/hmg/ddl195
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- Article
Type-2 diabetes: a cocktail of genetic discovery.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R202, doi. 10.1093/hmg/ddl191
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- Article
Untangling the tau gene association with neurodegenerative disorders.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R188, doi. 10.1093/hmg/ddl190
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- Article
The genetics of mental retardation.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R110, doi. 10.1093/hmg/ddl189
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- Article
Genetic susceptibility to myocardial infarction and coronary artery disease.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R117, doi. 10.1093/hmg/ddl183
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- Article
RNA-dominant diseases.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R162, doi. 10.1093/hmg/ddl181
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- Article
Challenges and opportunities in dystrophin-deficient cardiomyopathy gene therapy.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R253, doi. 10.1093/hmg/ddl180
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- Article
New techniques to understand chromosome dosage: mouse models of aneuploidy.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R103, doi. 10.1093/hmg/ddl179
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- Article
Signaling pathways in self-renewing hematopoietic and leukemic stem cells: do all stem cells need a niche?
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R210, doi. 10.1093/hmg/ddl175
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- Article
Signatures of adaptive evolution within human non-coding sequence.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R170, doi. 10.1093/hmg/ddl182
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- Article