"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes

BACKGROUND: Interstitial Microdeletion and Microduplication syndromes have been proposed as a significant cause of sporadic intellectual disability (ID) but the role of such aberrations in familial ID has not yet been investigated. As the balanced chromosomal abnormalities commonly lead to the recur...

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Hoofdauteurs: Rafati, Maryam, Seyyedaboutorabi, Elaheh, Ghadirzadeh, Mohammad R, Heshmati, Yaser, Adibi, Homeira, Keihanidoust, Zarrintaj, Eshraghian, Mohammad R, Javadi, Gholam Reza, Dastan, Jila, Mosavi-Jarrahi, Alireza, Hoseini, Azadeh, Purhoseini, Marzieh, Ghaffari, Saeed R
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2012
Onderwerpen:
Research
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3284449/
https://ncbi.nlm.nih.gov/pubmed/22283845
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-5-9
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