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C A Alper

Showing results (161-170 of 207) with videos related to

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Blood|December 1, 1989
Monoclonal and oligoclonal gammopathy after bone marrow transplantationA 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 pedigreeR 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 groupsD Corzo, J J Yunis, M Salazar, et al.
American Journal of Human Genetics|January 1, 1984
Human C4 haplotypes with duplicated C4A or C4BD 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 blocksE 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 variantsP M Schneider, M C Carroll, C A Alper, et al.
The Journal of Clinical Investigation|December 1, 1991
A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes)S Simon, Z Awdeh, R D Campbell, 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.
Clinical Immunology and Immunopathology|November 1, 1977
Homozygous C3 deficiency: detection of C3 by radioimmunoassayA E Davis, J S Davis, A R Rabson, et al.
Genes and Immunity|April 11, 2001
Hepatitis B surface antigen- and tetanus toxoid-specific clonal expansion of CD4+ cells in vitro determined by TCRBV CDR3 length and nucleotide sequenceG P Uko, P A Fraser, Z L Awdeh, et al.
Pageof 21

Showing results (161-170 of 207) with videos related to

Sort By:
Pageof 21
Blood|December 1, 1989
Monoclonal and oligoclonal gammopathy after bone marrow transplantationA 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 pedigreeR 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 groupsD Corzo, J J Yunis, M Salazar, et al.
American Journal of Human Genetics|January 1, 1984
Human C4 haplotypes with duplicated C4A or C4BD 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 blocksE 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 variantsP M Schneider, M C Carroll, C A Alper, et al.
The Journal of Clinical Investigation|December 1, 1991
A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes)S Simon, Z Awdeh, R D Campbell, 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.
Clinical Immunology and Immunopathology|November 1, 1977
Homozygous C3 deficiency: detection of C3 by radioimmunoassayA E Davis, J S Davis, A R Rabson, et al.
Genes and Immunity|April 11, 2001
Hepatitis B surface antigen- and tetanus toxoid-specific clonal expansion of CD4+ cells in vitro determined by TCRBV CDR3 length and nucleotide sequenceG P Uko, P A Fraser, Z L Awdeh, et al.
Pageof 21