Defining the common subtypes of HLA A9, A10, A28 and A19 by use of ARMS/PCR
- 1 July 1993
- journal article
- Published by Wiley in Tissue Antigens
- Vol. 42 (1) , 91-99
- https://doi.org/10.1111/j.1399-0039.1993.tb02173.x
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Tissue typing the HLA-A locus from genomic DNA by sequence-specific PCR: comparison of HLA genotype and surface expression on colorectal tumor cell lines.Proceedings of the National Academy of Sciences, 1993
- HLA-A locus alleles identified by sequence specific PCRThe Lancet, 1993
- Polymerase-chain-reaction-based analysis of polymorphism in the HLA-B geneHuman Immunology, 1992
- 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 transplantationTissue Antigens, 1992
- DNA typing for HLA class I alleles: I. Subsets of HLA-A2 and of -A28Human Immunology, 1992
- Rapid HLA‐DRB1 genotyping by nested PCR amplificationTissue Antigens, 1992
- A preliminary analysis of the 11.th International HistocompatibilitY Workshop monoclonal antibodies *Tissue Antigens, 1990
- Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)Nucleic Acids Research, 1989
- HLA-DR-DQ haplotypes defined by restriction fragment analysisHuman Immunology, 1987
- HLA Typing Using DNA ProbesBio/Technology, 1986