alexa MECP2 Duplication Syndrome.


Journal of Clinical & Medical Genomics

Author(s): Van Esch H

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Abstract Since the initial report that clearly established a causal role between duplication of the MECP2 gene and a severe syndromic form of intellectual disability, many new patients have been identified and reported, and the etiology in already published families solved. This has led to the establishment of a clinically recognizable disorder. Here, we review the clinical data of 129 reported and nonreported male patients with MECP2 duplication syndrome.
This article was published in Mol Syndromol and referenced in Journal of Clinical & Medical Genomics

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