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1. Nachweis einer erfolgreichen Knochenmarkstransplantation 11 Jahre nach Übertragung

2. Lambda and (Lambda)over-bar polarization from deep in elastic muon scattering

3. Nuclear decay following deep inelastic scattering of 470GeV muons (vol 74, pg 5198, 1995)

4. Extraction of the Ratio Fn2/Fp2 from Muon-Deuteron and Muon-Proton Scattering at Small x and Q2

5. Q2 dependence of the average squared transverse energy of jets in deep-inelastic muon-nucleon scattering with comparison to perturbative QCD predictions

6. STUDY OF PARTICLE SPECTRA WITH AN OPTICALLY READOUT RICH DETECTOR IN THE NA35 EXPERIMENT

7. Gonadoblastom bei einer HY-negativen reinen XY-Gonadendysgenesie

8. MULTIPLICITY AND TRANSVERSE ENERGY FLUX IN O-16+PB AT 200 GEV PER NUCLEON

9. CHARGED-PARTICLE MULTIPLICITIES AND INELASTIC CROSS-SECTIONS IN HIGH-ENERGY NUCLEAR COLLISIONS

10. PROBING THE SPACE-TIME GEOMETRY OF ULTRA-RELATIVISTIC HEAVY-ION COLLISIONS

11. Proton and deuteron structure functions in muon scattering at 470 GeV.

12. Nuclear decay following deep inelastic scattering of 470 GeV muons.

13. Measurement of nuclear transparencies from exclusive rho 0 meson production in muon-nucleus scattering at 470 GeV.

14. Scaled energy (z) distributions of charged hadrons observed in deep-inelastic muon scattering at 490 GeV from xenon and deuterium targets.

15. Perturbative QCD effects observed in 490 GeV deep-inelastic muon scattering.

16. First measurements of jet production rates in deep-inelastic lepton-proton scattering.

17. Saturation of shadowing at very low Bjorken x.

18. Cytogenetic effects during extracorporeal photopheresis treatment of two patients with cutaneous T-cell lymphoma.

19. Cardiac defects in chromosomally abnormal human embryos of 10-14 weeks' gestation.

20. [Partial deletion of the short arm of chromosome 13 as an indication of paternity in forensic assessment].

21. [Triploidy in newborn infants].

22. [Granulocyte function defects, chromosome anomalies and blood group chimerism in 2 sisters with familial aplastic anemia (Estren-Dameshek type)].

23. Report of a deletion 11 (qter----q23.3) and short review of the literature.

24. Possible origin of a small bisatellited additional chromosome.

25. [Syndrome of blue sclerae and keratoglobus (ocular type of Ehlers-Danlos syndrome (author's transl)].

26. Cri-du-chat syndrome in a child with a 5/15 translocation and interstitial centromeric heterochromatin.

28. [Familial nystagmus and hypoplasia of the macular in reciprocal, balanced translocation 5/16].

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