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  • Articles: DFG German National Licenses  (2)
  • 1995-1999  (2)
  • Prader-Willi syndrome  (1)
  • Spin arrangements in magnetically ordered materials (including neutron and spin-polarized electron studies, synchrotron-source X-ray scattering, etc.)  (1)
Source
  • Articles: DFG German National Licenses  (2)
Material
Years
  • 1995-1999  (2)
Year
Keywords
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Il nuovo cimento della Società Italiana di Fisica 18 (1996), S. 263-268 
    ISSN: 0392-6737
    Keywords: Spin arrangements in magnetically ordered materials (including neutron and spin-polarized electron studies, synchrotron-source X-ray scattering, etc.) ; Critical-point effects, specific heats short-range order ; Antiferromagnetics ; Conference proceedings
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Summary Mössbauer measurements have been made on two kinds of spin-glass (SG) systems: one is the magnetically non-diluted mixed compound Fe0.5Mn0.5TiO3 with the SG-freezing temperatureT SG=21.5K, and the other is the diluted one Fe0.2Mg0.8TiO3 withT SG=6K. We have shown that the temperature variation of the Mössbauer spectrum of Fe0.2Mg0.8TiO3 above and around itsT SG is essentially different from that of Fe0.5Mn0.5TiO3: the former is typical of a cluster-glass and the latter of an ordinary spin-glass. The present work has clearly demonstrated that the Mössbauer spectroscopy is the most useful and unique technique to distinguish a cluster-glass from an ordinary spin-glass.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of human genetics 44 (1999), S. 412-413 
    ISSN: 1435-232X
    Keywords: Key words XYY syndrome ; Prader-Willi syndrome ; Uniparental maternal disomy ; Non-disjunction of chromosome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract We report a 26-month-old boy with XYY syndrome, with the complication of Prader-Willi syndrome (PWS) due to uniparental maternal disomy of chromosome 15. To our knowledge, this is the first case of XYY syndrome and PWS. Clinical findings were fully compatible with the diagnostic criteria for PWS. Molecular analysis revealed a maternal heterodisomy of chromosome 15, indicating that non-disjunction of chromosome 15 had occurred at maternal meiosis I, and that the non-disjunction of chromosome Y and of chromosome 15 had occurred independently.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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