De novo interstitial triplication of MECP2 in a girl with neurodevelopmental disorder and random X chromosome inactivation.

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Published in Cytogenet Genome Res on September 16, 2011

Authors

S Mayo1, S Monfort, M Roselló, C Orellana, S Oltra, J Armstrong, V Català, F Martínez

Author Affiliations

1: Unidad de Genética y Diagnóstico Prenatal, Hospital Universitario La Fe, Valencia, Spain.

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