1[1]Brookes A J, Lehvaslaiho H, Siegfried M, et al.. A database of SNPs and other variations in and around human genes [J]. Nucleic Acids Research, 2000,28 (1): 356-360.
2[2]Brookes AJ.The essence of SNPs[J] .Gene,1999,234(2):177-186.
3[3]Taillon-Miller P, Gu Z, Li Q, et al. Overlapping genomic sequences: a treasure trove of single-nucleotide polymorphisms [J]. Genome Res,1998,8 (7): 748-754.
4[4]Lai E. Application of SNPs technologies in medicine :lessons learned and future challenges[ J]. Genome Res, 2001,11 (6) :927-929.
5[5]Cargill M, Altershuler D, Ireland J, et al. Characterization of single nucleotide polymorphisms in coding regions of human genes [J]. Nature Geneoms, 1999,22 ( 3 ): 231-238.
6[6]Barbujani G, Magagni A, Minch E, et al. An apportionment of human DNA diversity[J]. Proc Natl Acad Sci USA, 1997,94(9):4516-4519.
7[7]Wang DG, Fan JB, Sian CJ. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome[J]. Science, 1998,280(5366): 1077-1082.
8[8]Jiang R, Duan J, Windemuth A, et al. Genome-wide evaluation of the public SNP databases[J]. Pharmacogenomics,2003,4(6) :779-789.
9[9]Stephens JC, Schneider JA, Tanguay DA, et al. Haplotype variation and linkage disequilibrium in 313 human genes [J]. Science, 2001,293(5529): 489-493.
10[10]Horikawa Y, Oda N, Cox NJ, et al. Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus[J]. Nat Genet,2000,26(2) :163-175.
5Bitoun M,Maugenre S,Jeannet PY,et al.Mutation in dynamin2 cause dominant centronuclear myopathy [J].Nat Genet, 2005,37 : 1207-1209.
6The International SNP Map Working Group.A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms[J].Nature, 2001,409 : 928-933.
