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La ricerca find articoli where authors phrase all words ' Mimault, C' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 5 riferimenti
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    1. Cailloux, F; Gauthier-Barichard, F; Mimault, C; Isabelle, V; Courtois, V; Giraud, G; Dastugue, B; Boespflug-Tanguy, O
      Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    2. Mimault, C; Giraud, G; Courtois, V; Cailloux, F; Boire, JY; Dastugue, B; Boespflug-Tanguy, O
      Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher disease: Duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not

      AMERICAN JOURNAL OF HUMAN GENETICS
    3. MIMAULT C; COURTOIS V; GIRAUD G; BERTINI E; BAETHMANN M; FONTAN D; UZIEL G; VOIT T; BERNARD I; CAILLOUX F; BOESPFLUGTANGUY O
      DEVELOPMENTAL DEFECT OF MYELINATION RESULTING FROM PROTEOLIPID PROTEIN MUTATION IN HEREDITARY SPASTIC PARAPLEGIA OF CHILDHOOD

      Annals of neurology
    4. MIMAULT C; CAILLOUX F; GIRAUD G; DASTUGUE B; BOESPFLUGTANGUY O
      DINUCLEOTIDE REPEAT POLYMORPHISM IN THE PROTEOLIPOPROTEIN (PLP) GENE

      Human genetics
    5. BOESPFLUGTANGUY O; MIMAULT C; MELKI J; CAVAGNA A; GIRAUD G; DINH DP; DASTUGUE B; DAUTIGNY A; AICARDI J; GOUTTIERES F; BAUMANN N; BERTINI E; DAVID A; HENOCQ A; LANDRIEU P; TARDIEU M; LEBERRE C; LEMAREC B; LYON G; MAYER M; PINARD JM; PONSOT G; MATHIEU M; SAINTIVE JP; SAURA R; VALLEE L
      GENETIC HOMOGENEITY OF PELIZAEUS-MERZBACHER-DISEASE - TIGHT LINKAGE TO THE PROTEOLIPOPROTEIN LOCUS IN 16 AFFECTED FAMILIES

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/10/20 alle ore 22:57:55