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- 缺失型Midkinetruncated midkine (tMK)
- 缺失型α-地中海贫血deletional α -thalassemia
- QM-PCR证实7名缺失型患者中6名母亲是与缺失型患者相同的携带者(86.7%).The same deletions were readily demonstrated by QM -PCR in 6 of 7 mothers(86. 7%25) and one possible carrier was excluded.
- 型的thysanuriform
- Midkine基因Midkine
- 外型exterior
- 户型house type
- 笔型pen type
- 目的 对比分析缺失型杜氏肌营养不良症 (Duchenne muscular dystrophy,DMD)缺失热区第 46号和 51号外显子缺失后形成的连接片段的断裂点的分子结构特点 ,以研究 DMD基因外显子的缺失机理。Objective To study the exons deletion mechanisms for dystrophin gen e, the molecular characters of breakpoints of junction fragments for deletion-t y pe Duchenne muscular dystrophy (DMD) patients with 46 and 51 exons deletion were compared and analyzed.
- 选型lectotype
- 整型integer
- 房型house type
- 运动型motile
- 小型汽车roadlouse
- 基因型genotype
- 表型phenotype
- 压型profiling
- 构型configuration
- 经济型economical
- 外型尺寸external dimension
