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pro vyhledávání: '"B, Olaisen"'
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Akademický článek
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Publikováno v:
Clinical Genetics. 16:297-300
A study of the family of a patient who had an SLE-like syndrome and an extremely low serum C4 revealed an inheritance of C4 types and HLA region markers which indicated that the patient had 60--70% of "normal" C4 level prior to the onset of disease.
Autor:
S C Rall, Jr, K H Weisgraber, R W Mahley, C Ehnholm, O Schamaun, B Olaisen, J P Blomhoff, P Teisberg
Publikováno v:
Journal of Lipid Research, Vol 27, Iss 4, Pp 436-441 (1988)
An apolipoprotein (apo) A-I variant, previously described in two Norwegian families (Schamaun et al. 1983. Hum. Genet. 64: 380-383), represents a mutation in apoA-I in which a single amino acid substitution of lysine for glutamic acid has taken place
Externí odkaz:
https://doaj.org/article/ddb0da5146c84575a04b9408a135404e
Autor:
C vanderHagen, L. Vanmaldergem, Tobias Gedde-Dahl, B Olaisen, P. Hilbert, B. Mevåg, M Stenersen, O. Trygstad, Jocelyne Magré, J. Weissenbach, J Copeau, C Desbois-Mouthon, S. Fauré, Corinne Vigouroux
Publikováno v:
Scopus-Elsevier
Five of the six families with the Berardinelli-Seip syndrome in Norway cluster in six adjacent rural municipalities of south-western Norway. The six patients from this area were born between 1951 and 1973, none between 1974 and 1995. The absence of n
Publikováno v:
Reproduction. 99:421-425
The concentrations of lead in blood and the concentrations of lead, cadmium and zinc in tissues were determined in various reproductive organs, liver and kidney removed at necropsy from 41 men who had died suddenly. None of the reproductive organs sp
Autor:
W, Bär, B, Brinkmann, B, Budowle, A, Carracedo, P, Gill, M, Holland, P J, Lincoln, W, Mayr, N, Morling, B, Olaisen, P M, Schneider, G, Tully, M, Wilson
Publikováno v:
Vox sanguinis. 79(2)
Autor:
B, Olaisen, W, Bär, B, Brinkmann, B, Budowle, A, Carracedo, P, Gill, P, Lincoln, W R, Mayr, S, Rand
Publikováno v:
Vox sanguinis. 74(1)
The DNA commission of the International Society for Forensic Haemogenetics (ISFH) has over the years published a series of documents providing guidelines and recommendations concerning the application of DNA polymorphisms to problems of identificatio
Autor:
B, Olaisen
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 117(8)
Publikováno v:
International journal of legal medicine. 110(4)