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La ricerca find articoli where authors phrase all words ' DELEUZE JF' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 18 riferimenti
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    1. Emsley, RA; Niehaus, DJH; Mbanga, NI; Oosthuizen, PP; Stein, DJ; Maritz, JS; Pimstone, SN; Hayden, MR; Laurent, C; Deleuze, JF; Mallet, J
      The factor structure for positive and negative symptoms in South African Xhosa patients with schizophrenia

      SCHIZOPHRENIA RESEARCH
    2. Mujaheed, M; Corbex, M; Lichtenberg, P; Levinson, DF; Deleuze, JF; Mallet, J; Ebstein, RP
      Evidence for linkage by transmission disequilibrium test analysis of a chromosome 22 microsatellite marker D22S278 and bipolar disorder in a Palestinian Arab population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    3. Levinson, DF; Holmans, P; Straub, RE; Owen, MJ; Wildenauer, DB; Gejman, PV; Pulver, AE; Laurent, C; Kendler, KS; Walsh, D; Norton, N; Williams, NM; Schwab, SG; Lerer, B; Mowry, BJ; Sanders, AR; Antonarakis, SE; Blouin, JL; DeLeuze, JF; Mallet, J
      Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophrenia linkage collaborative group III

      AMERICAN JOURNAL OF HUMAN GENETICS
    4. Rust, S; Rosier, M; Funke, H; Real, J; Amoura, Z; Piette, JC; Deleuze, JF; Brewer, HB; Duverger, N; Denefle, P; Assmann, G
      Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

      NATURE GENETICS
    5. Bonnet-Brilhault, F; Laurent, C; Campion, D; Thibaut, F; Lafargue, C; Charbonnier, F; Deleuze, JF; Menard, JF; Jay, M; Petit, M; Frebourg, T; Mallet, J
      No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    6. TRIOCHE P; LABRUNE P; ODIEVRE M; HEDCHOUEL M; DELEUZE JF
      NOVEL MUTATION (G188R) IN THE G6PASE GENE OF A PATIENT WITH GLYCOGEN-STORAGE-DISEASE TYPE 1A

      Human mutation
    7. DEVREE JML; JACQUEMIN E; STURM E; CRESTEIL D; BOSMA PJ; ATEN J; DELEUZE JF; DESROCHERS M; BURDELSKI M; BERNARD O; ELFERINK RPJO; HADCHOUEL M
      MUTATIONS IN THE MDR3 GENE CAUSE PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS

      Proceedings of the National Academy of Sciences of the United Statesof America
    8. COSTA C; COSTA JM; DELEUZE JF; LEGRAND A; HADCHOUEL M; BAUSSAN C
      SIMPLE, RAPID NONRADIOACTIVE METHOD TO DETECT THE 3 MOST PREVALENT HEREDITARY FRUCTOSE INTOLERANCE MUTATIONS

      Clinical chemistry
    9. JACQUEMIN E; DEVREE JML; STURM E; CRESTEIL D; BOSMA PJ; ATEN J; DELEUZE JF; DESROCHERS M; BURDELSKI M; BERNARD O; HADCHOUEL M; ELFERINK RPJO
      MUTATIONS IN THE MDR3 GENE ARE RESPONSIBLE FOR A SUBTYPE OF PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS (PFIC)

      Hepatology
    10. DELEUZE JF; HADCHOUEL M
      DERMATOLOGICAL SYMPTOMS OF ALAGILLES SYND ROME - RESPONSE

      Gastroenterologie clinique et biologique
    11. DELEUZE JF; JACQUEMIN E; DUBUISSON C; CRESTEIL D; DUMONT M; ERLINGER S; BERNARD O; HADCHOUEL M
      DEFECT OF MULTIDRUG-RESISTANCE-3 GENE-EXPRESSION IN A SUBTYPE OF PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS

      Hepatology
    12. POLLET N; DHORNEPOLLET S; DELEUZE JF; BOCCACCIO C; DRIANCOURT C; RAYNAUD N; LEPASLIER D; HADCHOUEL M; MEUNIERROTIVAL M
      CONSTRUCTION OF A 3.7-MB PHYSICAL MAP WITHIN HUMAN-CHROMOSOME 20P12 ORDERING 18 MARKERS IN THE ALAGILLE SYNDROME LOCUS

      Genomics
    13. DELEUZE JF; DHORNEPOLLET S; POLLET N; MEUNIERROTIVAL M; HADCHOUEL M
      ALAGILLE-SYNDROME IN 1995 - CLINICAL AND GENETIC DATA

      Gastroenterologie clinique et biologique
    14. DELEUZE JF; DHORNE S; HAZAN J; BORGHI E; RAYNAUD N; POLLET N; MEUNIERROTIVAL M; DESCHATRETTE J; ALAGILLE D; HADCHOUEL M
      DELETED CHROMOSOME-20 FROM A PATIENT WITH ALAGILLE-SYNDROME ISOLATED IN A CELL HYBRID THROUGH LEUCINE TRANSPORT SELECTION - STUDY OF 3 CANDIDATE GENES

      Mammalian genome
    15. DELEUZE JF; DHORNE S; HAZAN J; BORGHI E; RAYNAUD N; POLLET N; MEUNIERROTIVAL M; DESCHATRETTE J; ALAGILLE D; HADCHOUEL M
      DELETED CHROMOSOME-20 FROM A PATIENT WITH ALAGILLE-SYNDROME ISOLATED IN A CELL HYBRID THROUGH LEUCINE TRANSPORT SELECTION - STUDY OF 3 CANDIDATE GENES

      Mammalian genome
    16. SMITH CL; KEITH T; HANSMANN I; WEISSENBACH J; ASIMAKOPOULOS FA; BOWDEN DW; DELEUZE JF; DUTTON ER; FASMAN KH; GREEN T; HADCHOUEL M; HAZAN J; HILGARTNER S; KINGSBURY DK; LODER B; MALAFOSSE A; MEUNIERROTIVAL M; PEARSON PL; SIRACUSA LD; STEINLEIN O; WHITE N; WILLIAMSON CM
      REPORT OF THE FIRST ERNATIONAL-WORKSHOP-ON-HUMAN-CHROMOSOME-20-MAPPING 1993 HELD ON SEPTEMBER 6-8, 1993 AT GIF-SUR-YVETTE, FRANCE

      Cytogenetics and cell genetics
    17. DHORNEPOLLET S; DELEUZE JF; HADCHOUEL M; BONAITIPELLIE C
      SEGREGATION ANALYSIS OF ALAGILLE SYNDROME

      Journal of Medical Genetics
    18. PEUDENIER S; DELEUZE JF; PHAMDINH D; LACROIX C; BOULLOCHE J; LANDRIEU P
      INFANTILE NEUROPATHY WITH UNSTABLE MYELIN - STUDY OF THE PO PROTEIN

      Journal of neurology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 02/06/20 alle ore 20:55:07