2003, 20(7):13-14.
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2003, 20(7):14-15.
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2003, 20(7):16-18.
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2003, 20(7):19-19.
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2003, 20(7):20-21.
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沈海娥 , 郭福生 , 龚振华 , 孙淑芳 , 裘孝良 , 郝勤宗
2003, 20(7):21-23.
摘要:Two pairs of primers were synthesized based on Sgene nucleotide sequences of transmissible qastroenteritis virus and porcine respiratory coronavirus.PCR was developed to amplify specifi squences,using TGEV and PRCV cell cultures as template.The amplified segment of TGEV gene was886bp and that of PRCV gene was214bp.Results showed that the n=pcr was rapid,specific and sensitive in detecting the clinical samples.
2003, 20(7):33-33.
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2003, 20(7):36-36.
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2003, 20(7):38-40.
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2003, 20(7):41-42.
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2003, 20(7):43-44.
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2003, 20(7):44-46.
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