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"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes.
Mol Cytogenet. 2012 Jan 29;5(1):9. doi: 10.1186/1755-8166-5-9.
Mol Cytogenet. 2012.
PMID: 22283845
Free PMC article.
Familial Williams-Beuren syndrome ascertained by screening rather than targeted diagnosis.
Rafati M, Seyyedaboutorabi E, Brujerdi R, Moossavi S, Ghaffari SR.
Rafati M, et al. Among authors: seyyedaboutorabi e.
Clin Dysmorphol. 2012 Jul;21(3):118-123. doi: 10.1097/MCD.0b013e3283520539.
Clin Dysmorphol. 2012.
PMID: 22473150
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