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

Pubmed ID: 
17712354
Year: 
2007
Month: 
Dec
Volume: 
15
Issue: 
12
Citation: 
Hardwick SA, Reuter K, Williamson SL, Vasudevan V, Donald J, Slater K, Bennetts B, Bebbington A, Leonard H, Williams SR, Smith RL, Cloosterman D, Christodoulou J. Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband. European journal of human genetics : EJHG 15 (12) : 1218 - 29(2007) PubMed