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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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Bibliographic Details
Main Authors: Froyen, Guy, Bauters, Marijke, Voet, Thierry, Marynen, Peter
Format: Artigo
Language:Inglês
Published: John Wiley & Sons, Ltd 2006
Subjects:
Online Access: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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