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Showing results (141-150 of 146) with videos related to

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Radiation Protection Dosimetry|May 16, 2006
Pitfalls and modelling inconsistencies in computational radiation dosimetry: lessons learnt from the QUADOS intercomparison. Part I: Neutrons and uncertaintiesB R L Siebert, R J Tanner, J-L Chartier, et al.
Radiation Protection Dosimetry|December 31, 2005
QUADOS intercomparison: a summary of photon and charged particle problemsG Gualdrini, S Agosteo, S Ménard, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1979
A twin methodology for the study of genetic and environmental control of variation in human smoking behaviorD W Crumpacker, R Cederlöf, L Friberg, et al.
Human Molecular Genetics|September 25, 1997
A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22G J Feldman, D E Ward, E Lajeunie-Renier, et al.
Radiation Protection Dosimetry|September 11, 2008
Analysis of the CONRAD computational problems expressing only stochastic uncertainties: neutrons and protonsG Gualdrini, R J Tanner, S Agosteo, et al.
Nature Genetics|December 1, 1995
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2N H Robin, G J Feldman, A L Aronson, et al.
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Showing results (141-150 of 146) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 146 results.
Radiation Protection Dosimetry|May 16, 2006
Pitfalls and modelling inconsistencies in computational radiation dosimetry: lessons learnt from the QUADOS intercomparison. Part I: Neutrons and uncertaintiesB R L Siebert, R J Tanner, J-L Chartier, et al.
Radiation Protection Dosimetry|December 31, 2005
QUADOS intercomparison: a summary of photon and charged particle problemsG Gualdrini, S Agosteo, S Ménard, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1979
A twin methodology for the study of genetic and environmental control of variation in human smoking behaviorD W Crumpacker, R Cederlöf, L Friberg, et al.
Human Molecular Genetics|September 25, 1997
A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22G J Feldman, D E Ward, E Lajeunie-Renier, et al.
Radiation Protection Dosimetry|September 11, 2008
Analysis of the CONRAD computational problems expressing only stochastic uncertainties: neutrons and protonsG Gualdrini, R J Tanner, S Agosteo, et al.
Nature Genetics|December 1, 1995
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2N H Robin, G J Feldman, A L Aronson, et al.
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