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La ricerca find articoli where authors phrase all words ' OZELIUS L' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 19 riferimenti
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    1. Klein, C; Schumacher, K; Jacobs, H; Hagenah, J; Kis, B; Garrels, J; Schwinger, E; Ozelius, L; Pramstaller, P; Vieregge, P; Kramer, PL
      Association studies of Parkinson's disease and parkin polymorphisms

      ANNALS OF NEUROLOGY
    2. Niida, Y; Lawrence-Smith, N; Banwell, A; Hammer, E; Lewis, J; Beauchamp, RL; Sims, K; Ramesh, VL; Ozelius, L
      Analysis of both TCS1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosis

      HUMAN MUTATION
    3. BEAUCHAMP RL; BANWELL A; MCNAMARA P; JACOBSEN M; HIGGINS E; NORTHRUP H; SHORT P; SIMS K; OZELIUS L; RAMESH V
      EXON SCANNING OF THE ENTIRE TSC2 GENE FOR GERMLINE MUTATIONS IN 40 UNRELATED PATIENTS WITH TUBEROUS SCLEROSIS

      Human mutation
    4. KLEIN C; VIEREGGE P; HEIDE W; KEMPER B; HAGEDORNGREIWE M; HAGENAH J; VOLLMER C; BREAKEFIELD XO; KOMPF D; OZELIUS L
      EXCLUSION OF CHROMOSOME REGIONS 6P12 AND 15Q11, BUT NOT CHROMOSOME REGION 7P11, IN A GERMAN FAMILY WITH AUTOSOMAL-DOMINANT CONGENITAL NYSTAGMUS

      Genomics (San Diego, Calif.)
    5. OZELIUS L; ATTWOOD J; REBELLO M; POVEY S; BREAKEFIELD X
      USE OF MEIOTIC BREAKPOINT PANEL TO MAP MARKERS INTO THE INTERVAL BETWEEN D9S60 AND ABL

      Annals of Human Genetics
    6. MCINTOSH L; CLOUGH MV; SCHAFFER AA; PUFFENBERGER EG; HORTON VK; PETERS K; ABBOTT MH; ROIG CM; CUTONE S; OZELIUS L; KWIATKOWSKI DJ; PYERITZ RE; BROWN LJ; PAULI RM; MCCORMICK MK; FRANCOMANO CA
      FINE MAPPING OF THE NAIL-PATELLA SYNDROME LOCUS AT 9Q34

      American journal of human genetics
    7. RISCH N; DELEON D; OZELIUS L; KRAMER P; ALMASY L; SINGER B; FAHN S; BREAKEFIELD X; BRESSMAN S
      GENETIC-ANALYSIS OF IDIOPATHIC TORSION DYSTONIA IN ASHKENAZI JEWS ANDTHEIR RECENT DESCENT FROM A SMALL FOUNDER POPULATION

      Nature genetics
    8. RISCH N; DELEON D; FAHN S; BRESSMAN S; OZELIUS L; BREAKEFIELD X; KRAMER P; ALMASY L; SINGER B
      ITD IN ASHKENAZI JEWS - GENETIC DRIFT OR SELECTION - REPLY

      Nature genetics
    9. HOLMGREN G; OZELIUS L; FORSGREN L; ALMAY BGL; HOLMBERG M; KRAMER P; FAHN S; BREAKEFIELD XO
      ADULT-ONSET IDIOPATHIC TORSION DYSTONIA IS EXCLUDED FROM THE DYT1 REGION (9Q34) IN A SWEDISH FAMILY

      Journal of Neurology, Neurosurgery and Psychiatry
    10. CUTONE S; RUTTER M; OZELIUS L; MURRELL J; BUCKLER A; MCCORMICK MK
      PHYSICAL MAPPING OF HUMAN-CHROMOSOME SEGMENT 9Q34

      American journal of human genetics
    11. GASSER T; WSZOLEK ZK; TROFATTER J; OZELIUS L; UITTI RJ; LEE CS; GUSELLA J; PFEIFFER RF; CALNE DB; BREAKEFIELD XO
      GENETIC-LINKAGE STUDIES IN AUTOSOMAL-DOMINANT PARKINSONISM - EVALUATION OF 7 CANDIDATE GENES

      Annals of neurology
    12. WAHLSTROM J; OZELIUS L; KRAMER P; KYLLERMAN M; SCHUBACK D; FORSGREN L; HOLMGREN G; DRUGGE U; SANNER G; FAHN S; BREAKEFIELD XO
      THE GENE FOR FAMILIAL DYSTONIA WITH MYOCLONIC JERKS RESPONSIVE TO ALCOHOL IS NOT LOCATED ON THE DISTAL END OF 9Q

      Clinical genetics
    13. HENSKE EP; OZELIUS L; GUSELLA JF; HAINES JL; KWIATKOWSKI DJ
      A HIGH-RESOLUTION LINKAGE MAP OF HUMAN 9Q34.1

      Genomics
    14. DELEON D; KRAMER P; OZELIUS L; BREAKEFIELD X; FAHN S; BRESSMAN SB
      PHENOTYPIC-EXPRESSION OF THE DYT1 GENE - WHO IS THE CARRIER

      Annals of neurology
    15. HENSKE EP; OZELIUS L; GUSELLA JF; HAINES JL; KWIATKOWSKI DJ
      A HIGH-RESOLUTION LINKAGE MAP OF HUMAN 9Q34.1

      Cytogenetics and cell genetics
    16. OZELIUS L; KRAMER P; BRESSMAN S; HEWETT J; DELEON D; RISCH N; FAHN S; BREAKEFIELD X
      DYSTONIA GENE (DYT1) ON CHROMOSOME-9Q34 APPEARS TO BE RESPONSIBLE FORMOST EARLY-ONSET CASES

      Cytogenetics and cell genetics
    17. BRESSMAN SB; HEIMAN G; HUNT A; OZELIUS L; NYGAARD T; BRIN M; MOSKOWITZ CB; DELEON D; BURKE RE; FAHN S; RISCH N; BREAKEFIELD XO; KRAMER P
      EVIDENCE FOR GENETIC-HETEROGENEITY IN IDIOPATHIC TORSION DYSTONIA (ITD)

      Neurology
    18. OZELIUS L; BRESSMAN S; GASSER T; DELEON D; HEWETT J; HEIMAN G; HUNT A; NYGARRD T; MOSKOWITZ C; BRIN M; FAHN S; BREAKEFIELD XO; KRAMER P
      MOST EARLY-ONSET CASES OF DYSTONIA ARE CAUSED BY THE DYT1 GENE ON CHROMO-9Q34

      American journal of human genetics
    19. HENSKE EP; OZELIUS L; GUSELLA JF; HAINES JL; KWIATKOWSKI DJ
      DETAILED GENETIC AND PHYSICAL MAPPING OF THE TUBEROUS SCLEROSIS REGION OF 9Q34

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 23/01/21 alle ore 06:00:39