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La ricerca find articoli where authors phrase all words ' NORBY S' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 21 riferimenti
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    1. Saillard, J; Magalhaes, PJ; Schwartz, M; Rosenberg, T; Norby, S
      Mitochondrial DNA variant 11719G is a marker for the mtDNA haplogroup cluster HV

      HUMAN BIOLOGY
    2. Rosser, ZH; Zerjal, T; Hurles, ME; Adojaan, M; Alavantic, D; Amorim, A; Amos, W; Armenteros, M; Arroyo, E; Barbujani, G; Beckman, G; Beckman, L; Bertranpetit, J; Bosch, E; Bradley, DG; Brede, G; Cooper, G; Corte-Real, HBSM; de Knijff, P; Decorte, R; Dubrova, YE; Evgrafov, O; Gilissen, A; Glisic, S; Golge, M; Hill, EW; Jeziorowska, A; Kalaydjieva, L; Kayser, M; Kivisild, T; Kravchenko, SA; Krumina, A; Kucinskas, V; Lavinha, J; Livshits, LA; Malaspina, P; Maria, S; McElreavey, K; Meitinger, TA; Mikelsaar, AV; Mitchell, RJ; Nafa, K; Nicholson, J; Norby, S; Pandya, A; Parik, J; Patsalis, PC; Pereira, L; Peterlin, B; Pielberg, G; Prata, ML; Previdere, C; Roewer, L; Rootsi, S; Rubinsztein, DC; Saillard, J; Santos, FR; Stefanescu, G; Sykes, BC; Tolun, A; Villems, R; Tyler-Smith, C; Jobling, MA
      Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language

      AMERICAN JOURNAL OF HUMAN GENETICS
    3. Richards, M; Macaulay, V; Hickey, E; Vega, E; Sykes, B; Guida, V; Rengo, C; Sellitto, D; Cruciani, F; Kivisild, T; Villems, R; Thomas, M; Rychkov, S; Rychkov, O; Rychkov, Y; Golge, M; Dimitrov, D; Hill, E; Bradley, D; Romano, V; Cali, F; Vona, G; Demaine, A; Papiha, S; Triantaphyllidis, C; Stefanescu, G; Hatina, J; Belledi, M; Di Rienzo, A; Novelletto, A; Oppenheim, A; Norby, S; Al-Zaheri, N; Santachiara-Benerecetti, S; Scozzari, R; Torroni, A; Bandelt, HJ
      Tracing European founder lineages in the near eastern mtDNA pool

      AMERICAN JOURNAL OF HUMAN GENETICS
    4. Saillard, J; Forster, P; Lynnerup, N; Bandelt, HJ; Norby, S
      mtDNA variation among Greenland Eskimos: The edge of the Beringian expansion

      AMERICAN JOURNAL OF HUMAN GENETICS
    5. Torroni, A; Richards, M; Macaulay, V; Forster, P; Villems, R; Norby, S; Savontaus, ML; Huoponen, K; Scozzari, R; Bandelt, HJ
      mtDNA haplogroups and frequency patterns in Europe

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. VISSING J; SALAMON MB; ARLIENSOBORG P; NORBY S; MANTA P; DIMAURO S; SCHMALBRUCH H
      A NEW MITOCHONDRIAL TRNA(MET) GENE MUTATION IN A PATIENT WITH DYSTROPHIC MUSCLE AND EXERCISE INTOLERANCE

      Neurology
    7. MACKEY D; OOSTRA RJ; ROSENBERG T; NIKOSKELAINEN E; POULTON J; BARRATT T; BOLHUIS P; NORBY S; SAVONTAUS ML; CHAN C; HOWELL N
      REPLY TO HOFMANN ET-AL

      American journal of human genetics
    8. SCHWARTZ M; SORENSEN N; HANSEN FJ; HERTZ JM; NORBY S; TRANEBJAERG L; SKOVBY F
      QUANTIFICATION, BY SOLID-PHASE MINISEQUENCING, OF THE TELOMERIC AND CENTROMERIC COPIES OF THE SURVIVAL MOTOR-NEURON GENE IN FAMILIES WITH SPINAL MUSCULAR-ATROPHY

      Human molecular genetics
    9. VELDHUISEN B; SARIS JJ; DEHAIJ S; HAYASHI T; REYNOLDS DM; MOCHIZUKI T; ELLES R; FOSSDAL R; BOGDANOVA N; VANDIJK MA; COTO E; RAVINE D; NORBY S; VERELLENDUMOULIN C; BREUNING MH; SOMLO S; PETERS DJM
      A SPECTRUM OF MUTATIONS IN THE 2ND GENE FOR AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (PKD2)

      American journal of human genetics
    10. RUSSELL MB; DIAMANT M; NORBY S
      GENETIC-HETEROGENEITY OF MIGRAINE WITH AND WITHOUT AURA IN DANES CANNOT BE EXPLAINED BY MUTATION IN MTDNA NUCLEOTIDE PAIR-11084

      Acta neurologica Scandinavica
    11. MAGALHAES PJ; SJO O; NORBY S
      OCULAR MYOPATHY AND MITOCHONDRIAL-DNA DELETION - A PRESENTATION OF 7 NEWLY IDENTIFIED DANISH PATIENTS

      Acta ophthalmologica Scandinavica
    12. MACKEY DA; OOSTRA RJ; ROSENBERG T; NIKOSKELAINEN E; BRONTESTEWART J; POULTON J; HARDING AE; GOVAN G; BOLHUIS PA; NORBY S; BLEEKERWAGEMAKERS EM; SAVONTAUS ML; CHAN C; HOWELL N
      PRIMARY PATHOGENIC MTDNA MUTATIONS IN MULTIGENERATION PEDIGREES WITH LEBER HEREDITARY OPTIC NEUROPATHY

      American journal of human genetics
    13. BLACK GCM; CRAIG IW; OOSTRA RJ; NORBY S; ROSENBERG T; MORTEN K; LABORDE A; POULTON J
      LEBER HEREDITARY OPTIC NEUROPATHY - IMPLICATIONS OF THE SEX-RATIO FORLINKAGE STUDIES IN FAMILIES WITH THE 3460 ND1 MUTATION

      Eye
    14. OLSEN NK; HANSEN AW; NORBY S; EDAL AL; JORGENSEN JR; ROSENBERG T
      LEBERS HEREDITARY OPTIC NEUROPATHY ASSOCIATED WITH A DISORDER INDISTINGUISHABLE FROM MULTIPLE-SCLEROSIS IN A MALE HARBORING THE MITOCHONDRIAL-DNA 11778-MUTATION

      Acta neurologica Scandinavica
    15. NORBY S
      OPTING FOR SILENCE

      Nature
    16. NORBY S
      GENETIC DYET

      Nature
    17. NORBY S; LESTIENNE P; NELSON I; NIELSEN IM; SCHMALBRUCH H; SJO O; WARBURG M
      JUVENILE KEARNS-SAYRE SYNDROME INITIALLY MISDIAGNOSED AS A PSYCHOSOMATIC DISORDER

      Journal of Medical Genetics
    18. LEROY D; NORBY S
      A NEW HUMAN MESSENGER TRANSFER DNA POLYMORPHISM - TRANSFER RNA(GLN) 4336 (T-]C)/

      Clinical genetics
    19. PETERS DJM; SPRUIT L; SARIS JJ; RAVINE D; SANDKUIJL LA; FOSSDAL R; BOERSMA J; VANEIJK R; NORBY S; CONSTANTINOUDELTAS CD; PIERIDES A; BRISSENDEN JE; FRANTS RR; VANOMMEN GJB; BREUNING MH
      CHROMOSOME 4 LOCALIZATION OF A 2ND GENE FOR AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE

      Nature genetics
    20. NORBY S
      SCREENING FOR THE 2 MOST FREQUENT MUTATIONS IN LEBER HEREDITARY OPTICNEUROPATHY BY DUPLEX PCR BASED ON ALLELE-SPECIFIC AMPLIFICATION

      Human mutation
    21. NORBY S
      MUTATION-SPECIFIC PCR - A RAPID AND INEXPENSIVE DIAGNOSTIC METHOD, ASEXEMPLIFIED BY MITOCHONDRIAL-DNA ANALYSIS IN LEBERS HEREDITARY OPTIC NEUROPATHY

      DNA and cell biology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/02/20 alle ore 05:21:34