(Q35445817)
Statements
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Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases (English)
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Kammoun F
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de Roux N
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Boespflug-Tanguy O
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Vallée L
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Seng R
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Tardieu M
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Landrieu P
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Identifiers
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