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Träfflista för sökning "WFRF:(Chapman M. J.) srt2:(1995-1999)"

Sökning: WFRF:(Chapman M. J.) > (1995-1999)

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1.
  • Gale, S. J., et al. (författare)
  • Band termination spectroscopy in 157Er
  • 1995
  • Ingår i: Journal of Physics G: Nuclear and Particle Physics. - 0954-3899. ; 21:2, s. 193-213
  • Tidskriftsartikel (refereegranskat)abstract
    • The level scheme of 157Er has been extended from a spin region where the nucleus behaves as a prolate rotor to a region where the spin is produced by the alignment of all or most of the available valence nucleons along the symmetry axis of a weakly deformed oblate shape. The level scheme was established at high spin using up to four-fold gamma -ray coincidences detected in the Eurogam spectrometer following the reaction 114Cd( 48Ca,5n)157Er at a bombarding energy of 210 MeV. Particularly favoured states have been established at IK=69/2+, 81/2+, 71/2+, 77/2-, 87-/2 and 89-/2. Specific single-particle configurations are assigned to these special states by comparison with cranked Nilsson-Strutinsky calculations. These states are related to structures observed in the neighbouring nuclei 158Er and 157Ho. These data provide the spectrum of single-particle states for the lowest lying valence orbitals above the 146Gd closed core.
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2.
  • Rees, D C, et al. (författare)
  • Born to clot : the European burden.
  • 1999
  • Ingår i: British Journal of Haematology. - 0007-1048 .- 1365-2141. ; 105:2, s. 564-6
  • Tidskriftsartikel (refereegranskat)abstract
    • Venous thrombosis is a common problem, predominantly afflicting people of European origin. This European predisposition has been explained to some extent by the recent characterization of factor V Leiden, and the G20210A prothrombin variant. Although it is clear that factor V Leiden is largely confined to Europeans, the world distribution of the prothrombin variant is not known. We have analysed samples from 22 different non-European countries and shown that this prothrombin variant is very rare outside Europe: one case occurring in India. The reason for the confined distribution of these two mutations is unclear.
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