Author(s): Letourneau A, Antonarakis SE
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Abstract Down syndrome caused by trisomy 21 is a collection of phenotypes with variable expressivity and penetrance. The significant advances in exploring the human genome now provide the tools to better understand the contribution of trisomy 21 in the different manifestations of Down syndrome, and the functional links between the genome variability and the phenotypic variability. Copyright © 2012 Elsevier B.V. All rights reserved.
This article was published in Prog Brain Res
and referenced in Journal of Down Syndrome & Chromosome Abnormalities