The occurrence of translocation (15;17) in acute promyelocytic leukemia: An update
- 作者M. De Braekeleer
- 卷第23卷
- 期第3期
- 文件大小125.12KB
- 发表时间1986
- DOI10.1016/0165-4608(86)90190-1
- 页码275-277
Case 5-2006Cabot, Richard C.; Harris, Nancy Lee; Shepard, Jo-Anne O.; Ebeling, Sally H.; Peters, Christine C.; Walton, David S.; Mukai, Shizuo; Grabowski, Eric F.; Munzenrider, John E.; Dryja, Thaddeus P. · New England Journal of Medicine · 2006
Linkage of Genes for Human Esterase D and Hereditary RetinoblastomaMukai, Shizuo; Rapaport, Joyce M.; Shields, Jerry A.; Augsburger, James J.; Dryja, Thaddeus P. · American Journal of Ophthalmology · 1984
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosaKajiwara, Kazuto; Hahn, Lauri B.; Mukai, Shizuo; Travis, Gabriel H.; Berson, Eliot L.; Dryja, Thaddeus P. · 1991
Transgenic mice with a rhodopsin mutation (Pro23His): A mouse model of autosomal dominant retinitis pigmentosaOlsson, Jane E.; Gordon, Jon W.; Pawlyk, Basil S.; Roof, Dorothy; Hayes, Annmarie; Molday, Robert S.; Mukai, Shizuo; Cowley, Glenn S.; Berson, Eliot L.; Dryja, Thaddeus P. · 1992