您要查找的是不是:
- xeroderma pigmentosum, xeroderma pigmentosa 着色性干皮病, DNA修复酶缺乏病
- xeroderma pigmentosa 着色性干皮病
- xeroderma pigmentosa syndrome 着色性干皮综合征
- Ik denk het wordt geroepen retinitis pigmentosa. 我闻悉它某处。我接受提名为adminship 。
- Retinitis pigmentosa, or R.P, is a form of retinal degeneration. 视网膜炎或R.;P是视网膜变性的一种。
- Xeroderma pigmentosum is an autosomal recessive disease. 着色性干皮病是一种常染色体的退行性疾病。
- Urticaria pigmentosa with neutrophil infiltration was diagnosed. 诊断为伴中性粒细胞浸润的色素性荨麻疹。
- Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum. XPF轻微突变导致致癌倾向综合征着色性干皮病。
- The trio, who had lost almost all of their vision due to retinitis pigmentosa (RP). 他们由于患有色素性视网膜炎(rp)而几乎丧失了所有的视力。
- Objective To obtain more quantitative descriptive data of Chinese patients with xeroderma pigmentosum (XP). 目的获取我国着色性干皮病(XP)患者更多的临床定量描述数据。方法回顾分析了我国39例XP患者的临床资料。
- The trio,who had lost almost all of their vision due to retinitis pigmentosa (RP). 他们由于患有色素性视网膜炎(RP)而几乎丧失了所有的视力。
- Abstract: Objective To obtain more quantitative descriptive data of Chinese patients with xeroderma pigmentosum (XP). [摘 要] 目的 获取我国着色性干皮病(XP)患者更多的临床定量描述数据。
- Objective: To study the effects of rhodopsin (RHO) gene in autosomal dominant retinitis pigmentosa (adRP). 摘要目的:探讨视紫红质基因在视网膜色素变性疾病中的作用。
- Retinitis pigmentosa is one hereditary disease that cause blind eyes and have relatively high incidence of disease. 视网膜色素变性是一种遗传性致盲性眼病,发病率较高,危害性较大。
- Objective To observe the effect of pigmentosa retinae treated by Chinese herb medicine point injection. 目的观察中药配合穴位注射治疗视网膜色素变性的临床疗效。
- Takebe H , nishigroi C, Satoh Y. Genetics and skin cancer of xeroderma pigmentosum In Japan. Jpn J Canver Res, 1987, 78:1135. 章扬培韩文智.;着色性干皮病细胞研究新进展[J]
- It changed the codon CGA for Arginine to a terminator codon TGA and causes retinitis pigmentosa in the two families. 它使该基因编码精氨酸的遗传密码CGA变为终止密码TGA,引起发病。
- The retinitis pigmentosa(RP)is an hereditary disease which causes visual deficiency leading to blindness. 视网膜色素变性是一种具有遗传性的致盲性眼病。
- The mouse bid handles , finds out a pigmentosa about of each the central Shaanxi plain and color. 虽然又简单又无聊,你想过关,还真不容易。
- Methods 60 patients with pigmentosa retinae(spleen and kidney deficiency)were randomly divided into two groups. 方法将60例脾肾阳虚型视网膜色素变性患者随机分为2组。