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Journal of Autoimmunity
|
October 21, 2006
A genetic explanation for the rising incidence of type 1 diabetes, a polygenic disease
Z L Awdeh, Edmond J Yunis, Mark J Audeh, et al.
Arthritis and Rheumatism
|
October 1, 1990
Major histocompatibility complex genes and susceptibility to systemic lupus erythematosus
Z Fronek, L A Timmerman, C A Alper, et al.
Immunogenetics
|
January 1, 1987
Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Z Layrisse, C White, P Gunczler, et al.
Blood
|
December 1, 1989
Monoclonal and oligoclonal gammopathy after bone marrow transplantation
A J Mitus, R Stein, J M Rappeport, et al.
Neurology
|
June 1, 1987
The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree
R M Boustany, E Fleischnick, C A Alper, et al.
Blood
|
November 15, 1995
The major histocompatibility complex region marked by HSP70-1 and HSP70-2 variants is associated with clozapine-induced agranulocytosis in two different ethnic groups
D Corzo, J J Yunis, M Salazar, et al.
American Journal of Human Genetics
|
January 1, 1984
Human C4 haplotypes with duplicated C4A or C4B
D Raum, Z Awdeh, J Anderson, et al.
Tissue Antigens
|
July 16, 2003
Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks
E J Yunis, C E Larsen, M Fernandez-Viña, 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.
Human Immunology
|
January 23, 1998
Relationship between protein complotypes and DNA variant haplotypes: complotype-RFLP constellations (CRC)
S Simon, L Truedsson, D Marcus-Bagley, et al.
Page
of 31
Search research articles
Search
Showing results (251-260 of 310) with videos related to
Sort By:
Page
of 31
Journal of Autoimmunity
|
October 21, 2006
A genetic explanation for the rising incidence of type 1 diabetes, a polygenic disease
Z L Awdeh, Edmond J Yunis, Mark J Audeh, et al.
Arthritis and Rheumatism
|
October 1, 1990
Major histocompatibility complex genes and susceptibility to systemic lupus erythematosus
Z Fronek, L A Timmerman, C A Alper, et al.
Immunogenetics
|
January 1, 1987
Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Z Layrisse, C White, P Gunczler, et al.
Blood
|
December 1, 1989
Monoclonal and oligoclonal gammopathy after bone marrow transplantation
A J Mitus, R Stein, J M Rappeport, et al.
Neurology
|
June 1, 1987
The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree
R M Boustany, E Fleischnick, C A Alper, et al.
Blood
|
November 15, 1995
The major histocompatibility complex region marked by HSP70-1 and HSP70-2 variants is associated with clozapine-induced agranulocytosis in two different ethnic groups
D Corzo, J J Yunis, M Salazar, et al.
American Journal of Human Genetics
|
January 1, 1984
Human C4 haplotypes with duplicated C4A or C4B
D Raum, Z Awdeh, J Anderson, et al.
Tissue Antigens
|
July 16, 2003
Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks
E J Yunis, C E Larsen, M Fernandez-Viña, 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.
Human Immunology
|
January 23, 1998
Relationship between protein complotypes and DNA variant haplotypes: complotype-RFLP constellations (CRC)
S Simon, L Truedsson, D Marcus-Bagley, et al.
Page
of 31