Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband

Simon A. Hardwick, Kirsten Reuter, Sarah L. Williamson, Vidya Vasudevan, Jennifer Donald, Katrina Slater, Bruce Bennetts, Ami Bebbington, Helen Leonard, Simon R. Williams, Robert L. Smith, Desiree Cloosterman, John Christodoulou*

*Corresponding author for this work

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