1Ochman H, Gerber A S, Hartl D L. Genetic applications of an inverse polymerase chain reaction. Genetics, 1988, 120:621～623
2Arveiler B, Porteous D J. Amplification of end fragments of YAC recombinants by inverse polymerase chain reaction. Technique,1991, 3:24～28
3Akiyama K, Watanabe H, Tsukada S, et al. A novel method for constructing gene-targeting vectors. Nucleic Acids Res, 2000, 28:e77
4Shyamala V, Ames G F-L. Genomic walking by single-specificprimer polymerase chain reaction: SSP-PCR. Gene, 1989, 84:1～8
5Warshawsky D, Miller L. A rapid genomic walking technique based on ligation-mediated PCR and magnetic separation technology. Biotechniques, 1994, 16:792～798
6Moynihan T P, Markham A F, Robinson P A. Genomic analysis of human multigene families using chromosome-specific Vectorette PCR. Nucleic Acids Res, 1996, 24:4094～4095
7Sterky F, Holmberg A, Alexandersson G, et al. Direct sequencing of bacterial artificial chromosomes (BACs) and prokaryotic genomes by biotin-capture PCR. J Biotechnol, 1998, 60:119～129
8Kilstrup M, Kristiansen K N. Rapid genome walking: A simplified oligo-cassette mediated polymerase chain reaction using a single genome-specific primer. Nucleic Acids Res, 2000, 28:e55
9Yan Y X, An C C, Li L, et al. T-linker-specific ligation PCR (T-linker PCR): An advanced PCR technique for chromosome walking or for isolation of tagged DNA ends. Nucleic Acids Res,2003, 31: e68
10Parker J D, Rabinovitch P S, Burmer G C. Targeted gene walking polymerase chain reaction. Nucleic Acids Res, 1991, 19:3056～3060
