共 9 条
[1]
Intragenic deletions in 164 boys with Duchenne muscualr dystrophy (DMD) studies with dystrophin cDNA. Upadhyaya M,Smith RA,Thomas NST,et al. Clinical Genetics . 1990
[2]
Correlation of clinical and deletion data in Duchenne and Pecker muscular dystrophy. Hodgson S,Hart K,Abbs S,et al. Journal of Medical Genetics . 1989
[3]
The molecular basis for Duchenne versus Pecker muscular dystrophy : correlation of severity with type of deletion. Koenig M,Beggs AH,Moyer M,et al. The American Journal of Human Genetics . 1989
[4]
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. Koenig M,Monaco AP,Kunkel LM,et al. Cell . 1988
[5]
Correlation of nonsense sires in the lacl gene with specific codons in the nucleotide sequence. Miller JH. Coulondre C. Farahough PJ,et al. Nature . 1978
[6]
Short, direct repeats at the breakpoints of deletions of the reti-noblastoma gene. Canning S,Dryja TP. Proceedings of the National Academy of Sciences of the United States of America . 1989
[7]
Characterization of six partial deletions in the low density-lipoprotein (LDL) receptor gene causing familial hypercholesterolemia (FH). Langlois S. Kastelein JJ. Hayden MR,et al. The American Journal of Human Genetics . 1988
[8]
242 breakpoints in the 200 kb deletion prone P20 region of the DMD gene widely spread. Blonden LA,Grootscholten PM,Den Dunnen JT. et al. Genomics . 1991
[9]
DNA sequence with the chain terminating inhibitors. Sanger F,Nicklen S,Coulson AR,et al. Proceedings of the National Academy of Sciences of the United States of America . 1977