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- 缺失型Midkinetruncated midkine (tMK)
- 缺失型α-地中海貧血deletional α -thalassemia
- QM-PCR證實(shí)7名缺失型患者中6名母親是與缺失型患者相同的攜帶者(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
- 戶(hù)型house type
- 筆型pen type
- 目的 對比分析缺失型杜氏肌營(yíng)養不良癥 (Duchenne muscular dystrophy,DMD)缺失熱區第 46號和 51號外顯子缺失后形成的連接片段的斷裂點(diǎn)的分子結構特點(diǎn) ,以研究 DMD基因外顯子的缺失機理。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.
- 選型lectotype
- 整型integer
- 房型house type
- 運動(dòng)型motile
- 小型汽車(chē)roadlouse
- 基因型genotype
- 表型phenotype
- 壓型profiling
- 構型configuration
- 經(jīng)濟型economical
- 外型尺寸external dimension
