"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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Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2012
Schlagworte:
Research
Online Zugang: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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