DR “low‐resolution” PCR‐SSP typing — a correction and an up‐date

Tissue Antigens

Volumn 41, Issue 1, 1993, Pages 55-56

[No Author Info available]

Author keywords

[No Author keywords available]

Indexed keywords

HLA DR ANTIGEN; PRIMER DNA;

ALLELE; DNA SEQUENCE; ERROR; GENE AMPLIFICATION; HLA TYPING; HUMAN; LETTER; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ALLELES; HISTOCOMPATIBILITY ANTIGENS CLASS II; HISTOCOMPATIBILITY TESTING; HLA-DR ANTIGENS; HUMAN; NUCLEIC ACID HYBRIDIZATION; POLYMERASE CHAIN REACTION;

EID: 0027502359     PISSN: 00012815     EISSN: 13990039     Source Type: Journal    
DOI: 10.1111/j.1399-0039.1993.tb01979.x     Document Type: Letter

References (7)

1. HLA‐DR typing by PCR amplification with sequence‐specific primers (PCR‐SSP) in 2 hours: An alternative to serological DR typing in clinical practice including donor‐recipient matching in cadaveric transplantation
2. Nomenclature for factors of the HLA system, 1992
3. HLA Class II nucleotide sequences, 1992
4. HLA‐DR and ‐DQ gene polymorphism in West Africans is twice as extensive as in North European Caucasians: Evolutionary implications
5. Molecular characterization of a recombinant HLA‐DR1/DR2 haplotype
6. HLA‐DRB1*01 subtyping by allele‐specific PCR amplification: A sensitive, specific and rapid technique
7. Identification of the HLADRB1*04, ‐DRB1*07 and ‐DRB1*09 alleles by PCR amplification with sequence‐specific primers (PCR‐SSP) in 2 hours