Catalogo Articoli (Spogli Riviste)

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La ricerca find articoli where soggetti phrase all words 'CHROMOSOME 14Q11.2-Q13' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 10 riferimenti
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    1. Fan, XP; Dion, P; Laganiere, J; Brais, B; Rouleau, GA
      Oligomerization of polyalanine expanded PABPN1 facilitates nuclear proteinaggregation that is associated with cell death

      HUMAN MOLECULAR GENETICS
    2. Blumen, SC; Korczyn, AD; Lavoie, H; Medynski, S; Chapman, J; Asherov, A; Nisipeanu, P; Inzelberg, R; Carasso, RL; Bouchard, JP; Tome, FMS; Rouleau, GA; Brais, B
      Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene

      NEUROLOGY

    3. Short GCG expansions in the PAB II gene for oculopharyngeal muscular dystrophy and diagnostic thereof

      EXPERT OPINION ON THERAPEUTIC PATENTS
    4. Brais, B; Rouleau, GA; Bouchard, JP; Fardeau, M; Tome, FMS
      Oculopharyngeal muscular dystrophy

      SEMINARS IN NEUROLOGY
    5. Grewal, RP; Karkera, JD; Grewal, RK; Detera-Wadleigh, SD
      Mutation analysis of oculopharyngeal muscular dystrophy in Hispanic American families

      ARCHIVES OF NEUROLOGY
    6. UYAMA E; UCHINO M; CHATEAU D; TOME FMS
      AUTOSOMAL RECESSIVE OCULOPHARYNGODISTAL MYOPATHY IN LIGHT OF DISTAL MYOPATHY WITH RIMMED VACUOLES AND OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    7. GREWAL RP; CANTOR R; TURNER G; GREWAL RK; DETERAWADLEIGH SD
      GENETIC-MAPPING AND HAPLOTYPE ANALYSIS OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      NeuroReport
    8. CREEL GB; GIULIANI MJ; LACOMIS D; HOLBACH SM
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY - NON-FRENCH-CANADIAN PEDIGREES

      Muscle & nerve
    9. TONIN PN; MESMASSON AM; FUTREAL PA; MORGAN K; MAHON M; FOULKES WD; COLE DEC; PROVENCHER D; GHADIRIAN P; NAROD SA
      FOUNDER BRCA1 AND BRCA2 MUTATIONS IN FRENCH-CANADIAN BREAST AND OVARIAN-CANCER FAMILIES

      American journal of human genetics
    10. BRAIS B; BOUCHARD JP; GOSSELIN F; XIE YG; FARDEAU M; TOME FMS; ROULEAU GA
      USING THE FULL POWER OF LINKAGE ANALYSIS IN 11 FRENCH-CANADIAN FAMILIES TO FINE MAP THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY GENE

      Neuromuscular disorders


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/08/20 alle ore 09:00:47