Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' TROFATTER J' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 8 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. NURNBERGER JI; TROFATTER J; MAYEDA A; TARRICONE B; HOFSTETTER J; SIMON J; GRAHAME N; LAHIRI DK; BELKNAP J; HINGTGEN J
      QUANTITATIVE TRAIT LOCI FOR TRAITS RELATED TO AFFECTIVE-DISORDER IN INBRED STRAINS OF MICE

      American journal of medical genetics
    2. MURRELL J; TROFATTER J; RUTTER M; CUTONE S; STOTLER C; RUTTER J; LONG K; TURNER A; DEAVEN L; BUCKLER A; MCCORMICK MK
      A 500-KILOBASE REGION CONTAINING THE TUBEROUS SCLEROSIS LOCUS (TSC1) IN A 1.7-MEGABASE YAC AND COSMID CONTIG

      Genomics
    3. HOTAMISLIGIL GS; GIRMEN AS; FINK JS; TIVOL E; SHALISH C; TROFATTER J; BAENZIGER J; DIAMOND S; MARKHAM C; SULLIVAN J; GROWDON J; BREAKEFIELD XO
      HEREDITARY VARIATIONS IN MONOAMINE-OXIDASE AS A RISK FACTOR FOR PARKINSONS-DISEASE

      Movement disorders
    4. 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
    5. MACCOLLIN M; MOHNEY T; TROFATTER J; WERTELECKI W; RAMESH V; GUSELLA J
      DNA DIAGNOSIS OF NEUROFIBROMATOSIS .2. ALTERED CODING SEQUENCE OF THEMERLIN TUMOR-SUPPRESSOR IN AN EXTENDED PEDIGREE (VOL 270, PG 2316, 1993)

      JAMA, the journal of the American Medical Association
    6. LEBO RV; CHANCE PF; DYCK PJ; REDILAFLORES MT; LYNCH ED; GOLBUS MS; BIRD TD; KING MC; ANDERSON LA; HALL J; WIEGANT J; JIANG ZR; DAZIN PF; PUNNETT HH; SCHONBERG SA; MOORE K; SHULL MM; GENDLER S; HURKO O; LOVELACE RE; LATOV N; TROFATTER J; CONNEALLY PM
      CHROMOSOME 1 CHARCOT-MARIE-TOOTH DISEASE (CMT1B) LOCUS IN THE FC-GAMMA RECEPTOR GENE REGION (VOL 88, PG 1, 1991)

      Human genetics
    7. MACCOLLIN M; MOHNEY T; TROFATTER J; WERTELECKI W; RAMESH V; GUSELLA J
      DNA DIAGNOSIS OF NEUROFIBROMATOSIS-2 - ALTERED CODING SEQUENCE OF THEMERLIN TUMOR-SUPPRESSOR IN AN EXTENDED PEDIGREE

      JAMA, the journal of the American Medical Association
    8. MUSARELLA MA; KIRSHGESSNER C; TROFATTER J; MIYAKE Y; DEGENNARO L
      ASSIGNMENT OF THE GENE FOR INCOMPLETE CONGENITAL STATIONARY NIGHT BLINDNESS (CSNB2) TO PROXIMAL XP

      Investigative ophthalmology & visual science


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/01/21 alle ore 05:51:57