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Molecular screening of MECP2 gene in a cohort of Lebanese patients suspected with Rett syndrome: report on a mild case with a novel indel mutationCORBANI, S; CHOUERY, E; FAYYAD, J et al.JIDR. Journal of intellectual disability research (Print). 2012, Vol 56, pp 415-420, issn 0964-2633, 6 p., 4Article

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