共 50 条
- [3] Pathogenic mutations in two families with congenital cataract identified with whole-exome sequencing [J]. MOLECULAR VISION, 2013, 19 : 384 - 389
- [5] PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema [J]. The Cerebellum, 2017, 16 : 272 - 275
- [6] PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema [J]. CEREBELLUM, 2017, 16 (01): : 272 - 275
- [10] Pathway Mutations in Breast Cancer Using Whole-Exome Sequencing [J]. ONCOLOGY RESEARCH, 2020, 28 (02) : 107 - 116