Intragenic deletions in 21 duchenne muscular dystrophy (DMD)/becker muscular dystrophy (BMD) families studied with the dystrophin DNA: location of breakpoints on hindill and bill exon-containing fragment maps, meiotic and mitotic origin of the mutations
T. Darras, Basil et al., Intragenic deletions in 21 duchenne muscular dystrophy (DMD)/becker muscular dystrophy (BMD) families studied with the dystrophin DNA: location of breakpoints on hindill and bill exon-containing fragment maps, meiotic and mitotic origin of the mutations, American journal of human genetics , 43-II(5), 1988, pp. 620-629