Catalogo Articoli (Spogli Riviste)

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La ricerca find articoli where authors phrase all words ' Meyer, BF' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 17 riferimenti
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    1. Martignetti, JA; Al Aqeel, A; Al Sewairi, W; Boumah, CE; Kambouris, M; Al Mayouf, S; Sheth, KV; Al Eid, W; Dowling, O; Harris, J; Glucksman, MJ; Bahabri, S; Meyer, BF; Desnick, RJ
      Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome

      NATURE GENETICS
    2. Kambouris, M; Banjar, H; Moggari, I; Nazer, H; Al-Hamed, M; Meyer, BF
      Identification of novel mutations in Arabs with cystic fibrosis and their impact on the cystic fibrosis transmembrane regulator mutation detection rate in Arab populations

      EUROPEAN JOURNAL OF PEDIATRICS
    3. Vartanian, TP; Perritt, HH; Stewart, M; Blumenfield, ED; Taylor, J; Lindberg, A; Pitegoff, TM; Morgan, J; Plesser, R; Millard, C; Johnson, D; Cochetti, R; Ingis, S; Arasaratnam, N; Bruening, P; Burr, B; Cole, S; Crawford, S; Day, R; Herrman, J; Kamp, J; Kirsch, S; Maganeau, J; Michelotti, C; Sand, P; Sarna, S; Scarborough, K; Sheldon, A; Tasse, R; Westby, J; Wood, D; Blackmer, WS; Sullivan, M; Barr, L; Belanger, PG; Brill, J; Byrne, J; Cowan, S; Duncan, M; Febeo, JF; Fischer, LR; Fishman, L; Friend, A; Gilbert, F; Gizzarelli, AM; Greenwood, D; Grohowski, R; Grosso, A; Hart, S; Havercroft, JV; Hiller, J; Hornbeck, R; Ireland, O; Kirsch, S; Kohler, K; Leifer, D; Litan, R; Mabbitt, S; Maxeiner, J; Messing, J; Morton, D; Nebolsky, S; Plesser, R; Revell, M; Rohner, R; Schmid, L; Soloway, J; Sookman, B; Stanley, F; Tackaberry, P; Terribile, C; Trubow, G; Vastine, R; Walker, C; Warrington, J; Weinberg, H; Westby, J; Zahralddin, R; Ballon, I; Nuara, L; Judy, HL; Rodeman, SP; Binder, SG; Corwin, P; Duan, J; McTaggart, T; Peterson, B; Sutin, AN; Rosenbaum, JI; Goldberg, E; McGuigan, P; Quist, D; Cohen, L; Chaneles, SB; Kravitz, M; Gedid, J; Wolfe, CA; Barstow, E; Beard, B; Binder, SG; Burke, JJA; Gilbert, F; Goldberg, JM; Graves, LDW; Ling, T; Mantas, P; Messing, J; Meyer-Hauser, BF; Rustad, M; Sigel, SM; Stein, FW; Treiman, S; Tripp, M; Whalen, P; Geist, MA; Aciman, C; Bayne, C; Dumaw, K; Forzley, M; Gupta, S; Halperin, E; Hoffer, S; Hopkins, S; Mantas, P; Pamenter, D; Plotkin, MJ; Rice, DT; Balinsky, A; Romanek, B; Hand, G; Post, D; Wetzler, M; Stettner, B; Federow, H; Stephenson, HG; Hudson, R; Plotkin, MJ; Cobb, PVZ; Barden, K; Caldwell, K; Chan, A; Gutman, H; Katz, S; Lyford, C; Quirk, P; Advogados, N; Gates, A; Pamenter, D; Sun, YY; Tackaberry, P; Balinsky, A; Poidevin, B; Thomson, N; Agrawala, R; Tosi, E; Yoshimura, T; Graham, JA; Parlade, C; Harsany, A; Meyer-Hauser, B; Hor, S; Tarabal, A; Aldaz, A
      Achieving legal and business order in cyberspace: A report on global jurisdiction issues created by the Internet

      BUSINESS LAWYER
    4. Dzimiri, N; Basco, C; Moorji, A; Meyer, BF
      Angiotensin-converting enzyme polymorphism and the risk of coronary heart disease in the Saudi male population

      ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
    5. Kambouris, M; Meyer, BF
      Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3 - Reply

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Kambouris, M; Bohlega, S; Al-Tahan, A; Meyer, BF
      Localization of the gene for a novel autosomal recessive neurodegenerativeHuntington-like disorder to 4p15.3

      AMERICAN JOURNAL OF HUMAN GENETICS
    7. Banjar, H; Kambouris, M; Meyer, BF; Al-Mehaidib, A; Mogarri, I
      Geographic distribution of cystic fibrosis transmembrane regulator gene mutations in Saudi Arabia

      ANNALS OF TROPICAL PAEDIATRICS
    8. Diaz, GA; Gelb, BD; Ali, F; Sakati, N; Sanjad, S; Meyer, BF; Kambouris, M
      Sanjad-sakati and autosomal recessive Kenny-Caffey syndromes are allelic: Evidence for an ancestral founder mutation and locus refinement

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Al-Jishi, E; Meyer, BF; Rashed, MS; Al-Essa, M; Al-Hamed, MH; Sakati, N; Sanjad, S; Ozand, PT; Kambouris, M
      Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency

      CLINICAL GENETICS
    10. Dzimiri, N; Meyer, BF; Hussain, SS; Basco, C; Afrane, B; Halees, Z
      Relevance of apolipoprotein E polymorphism for coronary artery disease in the Saudi population

      ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
    11. QARI MH; KHALIL SH; KAMBOURIS M; MEYER BF
      MUTATION OF P16, P21 OR CYCLIN-DEPENDENT KINASE-4 IS RARE IN ACUTE LYMPHOBLASTIC-LEUKEMIA

      British Journal of Haematology
    12. ALJISHI E; MEYER BF; RASHED M; ALHAMED MH; SAKATI N; SANJAD S; OZAND PT; KAMBOURIS M
      MOLECULAR ANALYSES OF THE GLUTATHIONE SYNTHETASE (GSS) GENE IN PATIENTS WITH PYROGLUTAMIC ACIDURIA

      American journal of human genetics
    13. KAMBOURIS M; RAHBEENI Z; MEYER BF; ALYAMANI EA; OZAND PT; RAHSED M
      MUTATION SCREENING OF THE MCAD GENE IN PATIENTS WITH BIOCHEMICAL MEDIUM-CHAIN FATTY-ACID OXIDATION DEFECTS (MCFAOD)

      American journal of human genetics
    14. WEBB M; RAPHAEL CL; ASBAHR H; ERBER WN; MEYER BF
      THE DETECTION OF RHODAMINE-123 EFFLUX AT LOW-LEVELS OF DRUG-RESISTANCE

      British Journal of Haematology
    15. LAZZARO GE; MEYER BF; WILLIS JI; ERBER WN; HERRMANN RP; DAVIES JM
      THE SYNTHESIS OF A PEANUT AGGLUTININ-RICIN-A CHAIN CONJUGATE - POTENTIAL AS AN IN-VITRO PURGING AGENT FOR AUTOLOGOUS BONE-MARROW IN MULTIPLE-MYELOMA

      Experimental hematology
    16. MEYER BF
      THE 5 GOSPELS - THE SEARCH FOR THE AUTHENTIC WORDS OF JESUS - FUNK,RW, HOOVER,RW, JESUS-SEMINAR

      Interpretation
    17. MEYER BF
      THE HISTORICAL JESUS - THE LIFE OF A MEDITERRANEAN JEWISH PEASANT - CROSSAN,JD

      The Catholic Biblical quarterly


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/10/20 alle ore 17:49:57