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X-linked mental retardation and epigenetics
The search for the genetic defects in constitutional diseases has so far been restricted to direct methods for the identification of genetic mutations in the patients’ genome. Traditional methods such as karyotyping, FISH, mutation screening, positional cloning and CGH, have been complemented with n...
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| Main Authors: | , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
John Wiley & Sons, Ltd
2006
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3933076/ https://ncbi.nlm.nih.gov/pubmed/17125586 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1582-4934.2006.tb00526.x |
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