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La ricerca find articoli where authors phrase all words ' SERRE JL' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 21 riferimenti
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    1. Lia-Baldini, AS; Muller, F; Taillandier, A; Gibrat, JF; Mouchard, M; Robin, B; Simon-Bouy, B; Serre, JL; Aylsworth, AS; Bieth, E; Delanote, S; Freisinger, P; Hu, JCC; Krohn, HP; Nunes, ME; Mornet, E
      A molecular approach to dominance in hypophosphatasia

      HUMAN GENETICS
    2. Megarbane, A; Waked, N; Chouery, E; Moglabey, YB; Saliba, N; Mornet, E; Serre, JL; Slim, R
      Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers

      AMERICAN JOURNAL OF MEDICAL GENETICS
    3. Greco, L; Babron, MC; Corazza, GR; Percopo, S; Sica, R; Clot, F; Fulchignoni-Lataud, MC; Zavattari, P; Momigliano-Richiardi, P; Casari, G; Gasparini, P; Tosi, R; Mantovani, V; De Virgiliis, S; Iacono, G; D'Alfonso, A; Selinger-Leneman, H; Lemainque, A; Serre, JL; Clerget-Darpoux, F
      Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

      ANNALS OF HUMAN GENETICS
    4. Clot, F; Babron, MC; Percopo, S; Giordano, M; Bouguerra, F; Clerget-Darpoux, F; Greco, L; Serre, JL; Fulchignoni-Lataud, MC
      Study of two ectopeptidases in the susceptibility to celiac disease: Two newly identified polymorphisms of dipeptidylpeptidase IV

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    5. Zurutuza, L; Muller, F; Gibrat, JF; Taillandier, A; Simon-Buoy, B; Serre, JL; Mornet, E
      Correlations of genotype and phenotype in hypophosphatasia

      HUMAN MOLECULAR GENETICS
    6. Clot, F; Fulchignoni-Lataud, MC; Renoux, C; Percopo, S; Bouguerra, F; Babron, MC; Djilai-Saiah, I; Caillat-Zucman, S; Clerget-Darpoux, F; Greco, L; Serre, JL
      Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations

      TISSUE ANTIGENS
    7. MORNET E; TAILLANDIER A; PEYRAMAURE S; KAPER F; MULLER F; BRENNER R; BUSSIERE P; FREISINGER P; GODARD J; LEMERRER M; OURY JF; PLAUCHU H; PUDDU R; RIVAL JM; SUPERTIFURGA A; TOURAINE RL; SERRE JL; SIMONBOUY B
      IDENTIFICATION OF 15 NOVEL MUTATIONS IN THE TISSUE-NONSPECIFIC ALKALINE-PHOSPHATASE (TNSALP) GENE IN EUROPEAN PATIENTS WITH SEVERE HYPOPHOSPHATASIA

      European journal of human genetics
    8. MORNET E; TAILLANDIER A; PEYRAMAURE S; KAPER F; MULLER F; SERRE JL; SIMONBOUY B
      IDENTIFICATION OF 15 NOVEL MUTATIONS IN THE TISSUE-NONSPECIFIC ALKALINE-PHOSPHATASE GENE IN EUROPEAN PATIENTS WITH HYPOPHOSPHATASIA

      European journal of human genetics
    9. MULLER F; DOMMERGUES M; SIMONBOUY B; FEREC C; OURY JF; AUBRY MC; BESSIS R; VUILLARD E; DENAMUR E; BIENVENU T; SERRE JL
      CYSTIC-FIBROSIS SCREENING - A FETUS WITH HYPERECHOGENIC BOWEL MAY BE THE INDEX CASE

      Journal of Medical Genetics
    10. MORNET E; CHATEAU C; SIMONBOUY B; SERRE JL
      THE INTERMEDIATE ALLELES OF THE FRAGILE-X CGG REPEAT IN PATIENTS WITHMENTAL-RETARDATION

      Clinical genetics
    11. GRECO L; CORAZZA G; BABRON MC; CLOT F; FULCHIGNONILATAUD MC; PERCOPO S; ZAVATTARI P; BOUGUERRA F; DIB C; TOSI R; TRONCONE R; VENTURA A; MANTAVONI W; MAGAZZU G; GATTI R; LAZZARI R; GIUNTA A; PERRI F; IACONO G; CARDI E; DEVIRGILIIS S; CATALDO F; DEANGELIS G; MUSUMECI S; FERRARI R; BALLI F; BARDELLA MT; VOLTA U; CATASSI C; TORRE G; ELIAOU JF; SERRE JL; CLERGETDARPOUX F
      GENOME SEARCH IN CELIAC-DISEASE

      American journal of human genetics
    12. FULCHIGNONILATAUD MC; OLCHWANG S; SERRE JL
      THE FRAGILE-X CGG REPEAT SHOWS A MARKED LEVEL OF INSTABILITY IN HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER PATIENTS

      European journal of human genetics
    13. MORNET E; MULLER F; LENVOISEFURET A; DELEZOIDE AL; COL JY; SIMONBOUY B; SERRE JL
      SCREENING OF THE C677T MUTATION ON THE METHYLENETETRAHYDROFOLATE REDUCTASE GENE IN FRENCH PATIENTS WITH NEURAL-TUBE DEFECTS

      Human genetics
    14. CLERGETDARPOUX F; CLOT F; BABRON MC; MARGARITTEJEANNIN P; FULCHIGNONILATAUD MC; PERCOPO S; ZAVATTARI P; ELIAOU JF; SERRE JL; GRECO L
      HLA COMPONENT OF CELIAC-DISEASE

      American journal of human genetics
    15. BABRON MC; GRECO L; CLOT F; FULCHIGNONILATAUD MC; PERCOPO S; ZAVATTARI P; BOUGUERRA F; DIB C; ELIAOU JF; SERRE JL; CLERGETDARPOUX F
      SYSTEMATIC SEARCH OF GENETIC RISK-FACTORS IN CELIAC-DISEASE

      American journal of human genetics
    16. MORNET E; CHATEAU C; TAILLANDIER A; SIMONBOUY B; SERRE JL
      RECURRENT AND UNEXPECTED SEGREGATION OF THE FMR1 CGG REPEAT IN A FAMILY WITH FRAGILE-X SYNDROME

      Human genetics
    17. BARBAT B; BOGYO A; RAUXDEMAY MC; KUTTENN F; BOUE J; SIMONBOUY B; SERRE JL; BOUE A; MORNET E
      SCREENING OF CYP21 GENE-MUTATIONS IN 129 FRENCH PATIENTS AFFECTED BY STEROID 21-HYDROXYLASE DEFICIENCY

      Human mutation
    18. MORNET E; CHATEAU C; TAILLANDIER A; MONTAGNON M; SIMONBOUY B; SERRE JL; BOUE A
      FRAXAC2 INSTABILITY

      Nature genetics
    19. CLOT F; JAGER M; SIMONBOUY B; SERRE JL; AUPETITFAISANT B; MORNET E
      A POLYMORPHIC POLY-A SEQUENCE IN THE 5' REGION OF THE ALDOSYNTHASE (CYP11B2) GENE MAY BE USEFUL IN GENETIC DIAGNOSIS OF 11-BETA-HYDROXYLASEGENES DEFECTS

      Human genetics
    20. SERRE JL
      WHICH UPPER AGE LIMIT FOR SEMEN DONORS

      Contraception fertilite sexualite
    21. SERRE JL; FEINGOLD J
      CONDITIONS AND LIMITS OF CARRIER SCREENIN G FOR CYSTIC-FIBROSIS

      Revue d'epidemiologie et de sante publique


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/05/20 alle ore 18:28:19