着色性干皮病

着色性干皮病：二家系三例报告

Xeroderma pigmentosum - A Report of Three Cases from Two Families

着色性干皮病39例临床分析

Clinical Analysis of 39 Cases with Xeroderma Pigmentosum

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

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

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

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

一是着色性干皮病（XP），另一是Cockayne综合征（CS）。

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

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。

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 .

目的建立中国人着色性干皮病（xerodermapigmentosum，XP）患者成纤维细胞株，分析其遗传互补组及分布。

Objective To establish skin fibroblast cell strains derived from Chinese xeroderma pigmentosum ( XP ) patients and to analyze the genetic complementation group and distribution .

XPF轻微突变导致致癌倾向综合征着色性干皮病。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum .

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。

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 .

中国人着色性干皮病遗传互补组分析

Genetic complementation group analysis of xeroderma pigmentosum patients in China

着色性干皮病患者的免疫学研究

Xeroderma pigmentosum : immunological studies in the patients

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

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

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。

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 .