1Mostacciub MI ,et al. Pupulation data on benign and severe forms of x-1 inked muscular dystropy[J]. Hum Genet, 1987,75:217 - 220.
2Chamberlain J S ,Gibbs R A, Ranier J E ,et al. Multiplex PCR for the diagnosis of Ducheme muscular dystrophy. In Innis MA,Gelfand DH,Sninsky JJ and White TJ. PCR Protocol:A Guide to Methods and Applications[M]. Academic Press, New York : 1990. 272 - 281.
3Beggs A H, Koenig M, Boyce FM, et al. Detection of 98% of DMD/BMD gene deletion bypolymerase chain reaction[J]. Hun Genet,1990,86:45 - 48.
4Lee SH, Kwak IP, Cha KE, et al. Preimplantation diagnosis of nondeletion Duchenne muscular dystrophy ( DMD ) by linkage polymerase chain reaction analysis[J]. Mol Hum Reprod, 1998,4 ( 4 ) : 345 -349.
9Hussey ND, Donggui H, Froiland DA, et al. Analysis of five Duchenne muscular dystmphy exons and gender determination using conventional duplex polymerase chain reaction on single cells[J]. Mol Hum Repmd, 1999,5(11):1089 - 1094.
10Pierre F Ray, Michel Vekemans and Arnold Munnich. Single cell multiplex PCR amplification of five dystrophin gene exon combined with gender determination[J]. Molecular Human Reproduction ,2001,7(5):489-494.
5Thornhill AR, McGrath JA,Eady RA, et al. A comparison of different lysis buffers to assess allele dropout from single cells for preimplantation genetic diagnosis [J]. Prenat Diagn,2001,21(6) :490 - 497.
6Rechitsky S, Strom C, Verlinsky O, et al. Allele dropout in polar bodies and blastomeres [ J ]. J Assist Reprod Genet, 1998,15 (5) :253 - 257.
6Mostacciub MI, Lombardi A,Cambissa V,et al. Population data on benign and severe forms of x-linked muscular dystrophy [ J]. Hum Genet, 1987,75:217 - 220.