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Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases |
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期刊:Journal of medical genetics 作者:Kammoun F; de Roux N; Boespflug-Tanguy O; Vallée L; Seng R; et al 出版日期:2004/06/01 |
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(2025-6-4)