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- 家族性C5补体无能症 Lenier syndrome
- 肥胖性生殖无能症 dystrophia adiposogenitalis
- 目的探讨慢性肺源性心脏病患者血清补体C1q、C5、C9水平的变化及临床意义。 Objective To study the change and the clinical significance of complement C1q and C5 and C9 on serum in the chronic cor pulmonale patients.
- 家族性高胆固醇血症患者低密度脂蛋白受体基因新突变一例 Identification of one novel mutation of the low density lipoprotein receptor gene in Chinese patients with familial hypercholesterolemia
- 青岛地区新生儿脐血胆固醇测定早期筛查家族性高胆固醇血症 Early screening familial hypercholesterolemia through infant umbilical blood cholesterol testing
- 人血浆补体C_9的纯化 Purification of the Ninth Component of Human Complement (C9)
- 家族性高胆固醇血症家系低密度脂蛋白受体基因剪接突变的研究 Identification of a novel splice mutation of low density lipoprotein receptor gene in a Chinese family with familial hypercholesterolemia
- 特发性低补体血症 essential hypocomplcmeatemia
- "别继续以这种节奏节生活:你会得神经衰弱症的。" "Don't carry on living this pace: You'll wind up with a nervous breakdown"
- 适体 fit
- 次Schur补 Sub-Schur complement
- 亲和配体 affinity ligand
- 肥胖性生殖无能综合征 dysdrophia adiposogenitalis
- 肥粒体 [机] ferrite
- 白便症 white feces syndrome
- 原孢子体 protosporophore
- 原子性 atomicity
- 主智能体 main agent
- 原卟啉症 protoporphyria
- 性价比高 high performance cost ratio; highly cost effective
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