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De novo Interstitial Triplication of MECP2 in a Girl with Neurodevelopmental Disorder and Random X Chromosome Inactivation

✍ Scribed by Mayo, S.; Monfort, S.; Roselló, M.; Orellana, C.; Oltra, S.; Armstrong, J.; Català, V.; Martínez, F.

Book ID: 119985555
Publisher: S. Karger AG
Year: 2011
Tongue: French
Weight: 726 KB
Volume: 135
Category: Article
ISSN: 1424-8581
DOI: 10.1159/000330917

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