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La ricerca find articoli where soggetti phrase all words 'MECP2 gene' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 11 riferimenti
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    1. Vourc'h, P; Bienvenu, T; Beldjord, C; Chelly, J; Barthelemy, C; Muh, JP; Andres, C
      No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients

      EUROPEAN JOURNAL OF HUMAN GENETICS
    2. Girard, M; Couvert, P; Carrie, A; Tardieu, M; Chelly, J; Beldjord, C; Bienvenu, T
      Parental origin of de novo MECP2 mutations in Rett syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    3. Colantuoni, C; Jeon, OH; Hyder, K; Chenchik, A; Khimani, AH; Narayanan, V; Hoffman, EP; Kaufmann, WE; Naidu, S; Pevsner, J
      Gene expression profiling in postmortem Rett syndrome brain: Differential gene expression and patient classification

      NEUROBIOLOGY OF DISEASE
    4. Couvert, P; Bienvenu, T; Aquaviva, C; Poirier, K; Moraine, C; Gendrot, C; Verloes, A; Andres, C; Le Fevre, AC; Souville, I; Steffann, J; des Portes, V; Ropers, HH; Yntema, HG; Fryns, JP; Briault, S; Chelly, J; Cherif, B
      MECP2 is highly mutated in X-linked mental retardation

      HUMAN MOLECULAR GENETICS
    5. Kerr, AM
      Recent developments in Rett syndrome research

      CURRENT OPINION IN PSYCHIATRY
    6. Xiang, F; Stenbom, Y; Anvret, M; Hagberg, B
      Closely related Swedish Rett syndrome females - None with MECP2 mutation revealed

      NEUROPEDIATRICS
    7. Zappella, M; Meloni, I; Longo, I; Hayek, G; Renieri, A
      Preserved speech variants of the Rett syndrome: Molecular and clinical analysis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. Imessaoudene, B; Bonnefont, JP; Royer, G; Cormier-Daire, V; Lyonnet, S; Lyon, G; Munnich, A; Amiel, J
      MECP2 mutation in non-fatal, non-progressive encephalopathy in a male

      JOURNAL OF MEDICAL GENETICS
    9. Lebo, RV; Ikuta, T; Milunsky, JM; Milunsky, A
      Rett syndrome from quintuple and triple deletions within the MECP2 deletion hotspot region

      CLINICAL GENETICS
    10. Amano, K; Nomura, Y; Segawa, M; Yamakawa, K
      Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome

      JOURNAL OF HUMAN GENETICS
    11. Orrico, A; Lam, CW; Galli, L; Dotti, MT; Hayek, G; Tong, SF; Poon, PMK; Zappella, M; Federico, A; Sorrentino, V
      MECP2 mutation in male patients with non-specific X-linked mental retardation

      FEBS LETTERS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/02/20 alle ore 15:17:42