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Dive into the research topics of 'Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband'. Together they form a unique fingerprint.- Sort by
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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*
Research output: Contribution to journal › Article › peer-review