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Brain & Development|December 12, 2001
Spectrum of MECP2 mutations in Rett syndromeS S Lee, M Wan, U FranckeBrain & Development|December 12, 2001
Rethinking the fate of males with mutations in the gene that causes Rett syndromeC SchanenBrain & Development|December 12, 2001
Mutation analysis of the methyl-CpG-binding protein 2 gene (MECP2) in Rett patients with preserved speechY Yamashita, I Kondo, T Fukuda, et al.Brain & Development|December 12, 2001
Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys)S G Vorsanova, Y B Yurov, V Y Ulas, et al.Brain & Development|December 12, 2001
Head growth in Rett syndromeG Hagberg, Y Stenbom, I W EngerströmBrain & Development|December 12, 2001
Development of language in Rett syndromeJ Uchino, M Suzuki, K Hoshino, et al.Brain & Development|December 12, 2001
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved regionM Vacca, F Filippini, A Budillon, et al.Brain & Development|December 12, 2001
Rett syndrome in Spain: mutation analysis and clinical correlationsE Monrós, J Armstrong, E Aibar, et al.Brain & Development|December 12, 2001
A case of effective gastrostomy for severe abdominal distention due to breathing dysfunction of Rett's syndrome: a treatment of autonomic disorderY Anzai, T OhyaBrain & Development|August 16, 2001
Galactonojirimycin derivatives restore mutant human beta-galactosidase activities expressed in fibroblasts from enzyme-deficient knockout mouseL Tominaga, Y Ogawa, M Taniguchi, et al.Pageof 482