(Q48546504)
Statements
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Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females. (English)
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C Philippe
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D Amsallem
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C Francannet
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L Lambert
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A Saunier
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F Verneau
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P Jonveaux
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29 June 2009
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47
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1
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59-65
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Identifiers
1 reference