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European Journal of Pediatrics
|
December 1, 1989
Possible association of sudden infant death with partial complement C4 deficiency revealed by post-mortem DNA typing of HLA class II and III genes
P M Schneider, C Wendler, T Riepert, et al.
Immunogenetics
|
January 1, 1988
Antigenic determinants expressed by human C4 allotypes; a study of 325 families provides evidence for the structural antigenic model
C M Giles, B Uring-Lambert, J Goetz, et al.
Physical Review Letters
|
November 24, 2011
Metastability in spin-polarized Fermi gases
Y A Liao, M Revelle, T Paprotta, et al.
Human Genetics
|
July 12, 1978
Evidence for subtypic determinants in the HLA-DW3 cluster
D Niese, H Grosse-Wilde, B Dupont, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
May 15, 1997
The human complement C9 gene: identification of two mutations causing deficiency and revision of the gene structure
K Witzel-Schlömp, P J Späth, M J Hobart, et al.
Complement and Inflammation
|
January 1, 1990
C4 nomenclature statement (1990)
G Mauff, C A Alper, R Dawkins, et al.
Annals of the Rheumatic Diseases
|
March 13, 1998
No primary association between LMP2 polymorphisms and extraspinal manifestations in spondyloarthropathies
T Höhler, T Schäper, P M Schneider, et al.
The Journal of Clinical Investigation
|
September 1, 1986
Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants
P M Schneider, M C Carroll, C A Alper, et al.
Immunogenetics
|
June 20, 1998
Heterogeneity in the genetic basis of human complement C9 deficiency
K Witzel-Schlömp, M J Hobart, B A Fernie, et al.
Transplantation Proceedings
|
March 1, 1977
B-cell-specific alloantigens in recombinant families
E D Albert, S Scholz, B Kuntz, et al.
Page
of 17
Search research articles
Search
Showing results (141-150 of 162) with videos related to
Sort By:
Page
of 17
European Journal of Pediatrics
|
December 1, 1989
Possible association of sudden infant death with partial complement C4 deficiency revealed by post-mortem DNA typing of HLA class II and III genes
P M Schneider, C Wendler, T Riepert, et al.
Immunogenetics
|
January 1, 1988
Antigenic determinants expressed by human C4 allotypes; a study of 325 families provides evidence for the structural antigenic model
C M Giles, B Uring-Lambert, J Goetz, et al.
Physical Review Letters
|
November 24, 2011
Metastability in spin-polarized Fermi gases
Y A Liao, M Revelle, T Paprotta, et al.
Human Genetics
|
July 12, 1978
Evidence for subtypic determinants in the HLA-DW3 cluster
D Niese, H Grosse-Wilde, B Dupont, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
May 15, 1997
The human complement C9 gene: identification of two mutations causing deficiency and revision of the gene structure
K Witzel-Schlömp, P J Späth, M J Hobart, et al.
Complement and Inflammation
|
January 1, 1990
C4 nomenclature statement (1990)
G Mauff, C A Alper, R Dawkins, et al.
Annals of the Rheumatic Diseases
|
March 13, 1998
No primary association between LMP2 polymorphisms and extraspinal manifestations in spondyloarthropathies
T Höhler, T Schäper, P M Schneider, et al.
The Journal of Clinical Investigation
|
September 1, 1986
Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants
P M Schneider, M C Carroll, C A Alper, et al.
Immunogenetics
|
June 20, 1998
Heterogeneity in the genetic basis of human complement C9 deficiency
K Witzel-Schlömp, M J Hobart, B A Fernie, et al.
Transplantation Proceedings
|
March 1, 1977
B-cell-specific alloantigens in recombinant families
E D Albert, S Scholz, B Kuntz, et al.
Page
of 17