3Fortina P, Cheng J, Shoffner M A, et al. Diagnosis of Duchenne/ Becker muscular dystrophy and quantitative identification of carrier status by use of entangled solution capillary electrophoresis [J]. Clin Chem, 1997, 43(5) :745-751.
4Lee S H, Kwak I P, Cha K E, et al. Preimplantation diagnosis of non-deletion Duchenne muscular dystrophy (DMD) by linkage polymerase chain reaction analysis [J]. Mol Hum Reprod, 1998, 4 (4) : 345-349.
5Xiao Y, Jiang X, Wang R. Screening for DMD/BMD deletion carriers by fluorescence in situ hybridization [J]. Genet Test, 2003, 7(3) : 195-201.
6Mallikarjuna Rao G N, Hussain T, Geetha Devi N, et al. Dystrophin gene deletions in South Indian Duchenne muscular dystrophy patients[J]. Indian J Med Sci, 2003, 57( 1 ) : 1-6.
7Beggs A H, Koenig M, Boyce F M, et aL Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction [J]. Hum Genet, 1990, 86( 1 ):45-48.
8Blonden L A, den Dunnen J T, van Paassen H M, et al. High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization [J]. Nucleic Acids Res, 1989, 17(14):5611- 5621.
9Kim U K, Chae J J, Lee S H, et al. Molecular diagnosis of Duchenne/Becker muscular dystrophy by polymerase chain reaction and microsatellite analysis [J ]. Mol Cells, 2002, 13 (3) : 385-388.