"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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書誌詳細
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2012
主題:
Research
オンライン･アクセス: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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