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La ricerca find articoli where authors phrase all words 'Hand, CK' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 8 riferimenti
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    1. Hand, CK; Khoris, J; Salachas, F; Gros-Louis, F; Lopes, AAS; Mayeux-Portas, V; Brown, RH; Meininger, V; Camu, W; Rouleau, GA
      A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Hadano, S; Hand, CK; Osuga, H; Yanagisawa, Y; Otomo, A; Devon, RS; Miyamoto, N; Showguchi-Miyata, J; Okada, Y; Singaraja, R; Figlewicz, DA; Kwiatkowski, T; Hosler, BA; Sagie, T; Skaug, J; Nasir, J; Brown, RH; Scherer, SW; Rouleau, GA; Hayden, MR; Ikeda, JE
      A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 (vol 29, pg 166, 2001)

      NATURE GENETICS
    3. Hadano, S; Hand, CK; Osuga, H; Yanagisawa, Y; Otomo, A; Devon, RS; Miyamoto, N; Showguchi-Miyata, J; Okada, Y; Singaraja, R; Figlewicz, DA; Kwiatkowski, T; Hosler, BA; Sagie, T; Skaug, J; Nasir, J; Brown, RH; Scherer, SW; Rouleau, GA; Hayden, MR; Ikeda, JE
      A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

      NATURE GENETICS
    4. Hand, CK; Mayeux-Portas, V; Khoris, J; Briolotti, V; Clavelou, P; Camu, W; Rouleau, GA
      Compound heterozygosity and variable penetrance in SOD1 amyotrophic lateral sclerosis pedigrees - Reply

      ANNALS OF NEUROLOGY
    5. Hand, CK; Mayeux-Portas, V; Khoris, J; Briolotti, V; Clavelou, P; Camu, W; Rouleau, GA
      Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family

      ANNALS OF NEUROLOGY
    6. Dupre, N; Cossette, L; Hand, CK; Bouchard, JP; Rouleau, GA; Puymirat, J
      A founder mutation in French-Canadian families with X-linked hereditary neuropathy

      CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
    7. Hand, CK; Harmon, DL; Kennedy, SM; FitzSimon, JS; Collum, LMT; Parfrey, NA
      Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping

      GENOMICS
    8. Callaghan, M; Hand, CK; Kennedy, SM; FitzSimon, JS; Collum, LMT; Parfrey, NA
      Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct

      BRITISH JOURNAL OF OPHTHALMOLOGY


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/10/19 alle ore 05:05:18