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G and P tying of group A porcine rotaviruses (PoRV) from field fecal samples were performed using reversetranscriptase polymerization chain reaction (RT-PCR) and restriction fragment length polymorphism (RFLP) analysis. After amplifying full length VP7 and partial length VP4 genes, restriction endonucleases were used to digest and analyze the cutting pattern of the gene products. After analysis of digests with restriction endonucleases, seven and six RFLP types were observed for VP7 and VP4,doi:10.4167/jbv.2006.36.4.255 fatcat:zidpvrpz6vhgzn3d5imdh6npqq