2) autosomal dominant retinitis pigmentosa
常染色体显性遗传视网膜色素变性
1.
Objective To detect mutation in the rhodopsin gene ( RHO ) in a Chinese family with autosomal dominant retinitis pigmentosa (ADRP).
目的 确定常染色体显性遗传视网膜色素变性家系的致病基因及其突变位点,并研究其临床表型。
4) retinitis pigmentosa
视网膜色素变性
1.
Investigation on genetic linkage analysis of a family with X-linked retinitis pigmentosa;
一个疑似X连锁型视网膜色素变性家系的遗传连锁分析的研究
2.
Progress in the research of mutation of IMPDH1 gene and retinitis pigmentosa;
IMPDH1基因突变与视网膜色素变性的研究进展
3.
Mutations of the IMPDH1 gene in patients correlated with autosomal dominant retinitis pigmentosa family;
视网膜色素变性一家系与IMPDH1基因突变相关
5) pigmentary degeneration of retina
视网膜色素变性
1.
Clinic Study on Electric Acupuncture Function of Treating Pigmentary Degeneration of Retina;
电针治疗视网膜色素变性的临床研究
2.
OBJECTIVE:To investigate curative effect of combined therapy of chinese and western medicine treating primary pigmentary degeneration of retina.
目的 :探讨中西医结合治疗视网膜色素变性的临床疗效。
6) hereditary retinal degeneration
遗传性视网膜变性
1.
In order to investigate photoreceptor (PRC) apoptosis and gene regulation in hereditary retinal degeneration of Royal College of Surgeon (RCS) rats, the retinal sections of RCS and SD rats at different ages were examined by TUNEL and Fas protein immunohistochemical method.
为了探讨遗传性视网膜变性时感光细胞凋亡及其基因调控机制 ,本研究对出生后 9、15、2 0、2 5、3 0、3 5、40、60 d的 RCS大鼠及同龄 SD大鼠各 4只的视网膜进行了 TU NEL 凋亡检测及 Fas蛋白免疫组织化学反应。
补充资料：视网膜色素变性肥胖多指综合征
视网膜色素变性肥胖多指综合征
病名。即劳-穆-比综合征，详见该条。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条