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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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Библиографические подробности
Главные авторы: Froyen, Guy, Bauters, Marijke, Voet, Thierry, Marynen, Peter
Формат: Artigo
Язык:Inglês
Опубликовано: John Wiley & Sons, Ltd 2006
Предметы:
Online-ссылка: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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