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。

BACKGROUND & OBJECTIVE : Xeroderma pigmentosum group C ( XPC ) gene is involved in nucleotide excision repair ( NER ) .

背景与目的： XPC基因参与核苷酸切除修复，该基因存在单核苷酸多态性（SNP）位点，并 可能 通过SNP位点碱基的 改变影响其修复能力 及 疾病易感性。

Study of AND Repair Enzyme System I. Ultraviolet-Induced H-TdR Unscheduled Incorporations Xeroderma Pigmentosum Lymphocytes

DNA修复酶系统的研究&Ⅰ.紫外线诱发~3H-TdR在 着色 性 干皮病淋巴细胞中的非合成期掺入

Xeroderma pigmentosum - A Report of Three Cases from Two Families

着色 性 干皮病：二家系三例报告

I can think of a bunch of ailments ; undevelope ¬ d limbs immune systems gone Xeroderma Pigmentosa ( allergy to light ) .

我可以联想到一连串的疾病： 四肢瘫痪，免疫系统消失等。

DNA-based prenatal diagnosis in a Chinese family with xeroderma pigmentosum group A

1个有 遗传 性 A群 着色 性 干皮病的中国家庭的基于DNA的产前诊断

Xeroderma pigmentosum : immunological studies in the patients

着色 性 干皮病患者的免疫学研究

The results showed that the most common was verruca senilis ( 37.96 % ) followed by angioma senilis leukoderma guttata alopecia xeroderma and longitudinal crest of nails .

其次是点状血管瘤， 点状白斑，脱发，皮肤干燥及指甲纵嵴。

Establishment of the fibroblast cell line in the xeroderma pigmentosum patient and a study of its biological characteristics

着色性 干皮病皮肤成纤维细胞系 （ XP4SH）的建立及其生物学特性

Clinical Analysis of 39 Cases with Xeroderma Pigmentosum

着色 性 干皮病39例临床分析

One is Xeroderma Pigmentosum ( XP ) and the other is the Cockayne Syndrome ( OS ) .

一是 着色 性 干皮病（XP），另一是Cockayne综合征（CS）。

Objective To study the association between polymorphism of DNA repair gene xeroderma pigmentosum G ( XPG ) Asp1104His and the risks of developing laryngeal and hypopharyngeal carcinomas .

目的研究DNA修复基因 着色 性 干皮病G组基因（XPG）Asp1104His多态性与喉癌和喉咽癌风险的相关性。

Association between Genetic Polymorphism in Xeroderma Pigmentosum G Gene and Risks of Laryngeal and Hypopharyngeal Carcinomas

着色 性 干皮病G组基因多态性与喉癌和喉咽癌风险的相关性

Fourty fiue cases with xeroderma pigmentosum in 27 families reported by literatures in China from 1955 to 1985 . The age of patients at onset of the disease range from 3 months to 20 years .

本文分析了国内1955～1986年文献报道的27个家族45例 着色 性 干皮病。

Genetic complementation group analysis of xeroderma pigmentosum patients in China

中国 人 着色 性 干皮病遗传互补组分析

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。

Clinical data of 13 cases of xeroderma pigmentosum ( XP ) in 6 families collected in Ningxia region from 1984 to 1992 are presented . Among them 4 patients from 2 families were followed up for 8 years .

报告了1984～1992年宁夏地区6家系13例 着色 性 干皮病（XP）患者的临床及两家系4例患者长达8年的随访情况。

A Case of Xeroderma Pigmentosum Q & A on Sex

着色 性 干皮病1例