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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
