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Conclusion: Model choice is a critical yet neglected issue in genetical genomics studies.
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Hyperpepsinogenemia I is a reliable subclinical marker of the genetical predisposition to suffer duodenal ulcer.
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This rapid progress has been made possible by the generation of a genetical and physical map of the human genome.
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In tertiary ophthalmic practice in India, there is an emerging trend towards the application of genetical knowledge in clinical practice.
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We propose in this article several methods for testing genetical isochronism or detecting significant genetical heterochronism in this type of sample.
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Genetical tests detect CTG repeat expansion of the involved gene.
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He was the guest of the Trinity College Genetical Society.
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Background: Genetical genomics is a very powerful tool to elucidate the basis of complex traits and disease susceptibility.
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Genetical genomics studies have mainly focused on cell lines, blood cells or adipose tissues, from human clinical samples or mice inbred lines.