xeroderma pigmentosum

1. 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。
2. 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。
3. A Case of Xeroderma Pigmentosum Q& A on Sex
   着色性干皮病1例
4. 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
5. Xeroderma pigmentosum: immunological studies in the patients
   着色性干皮病患者的免疫学研究
6. 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。
7. 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。
8. 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
9. 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）。
10. 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
11. 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。
12. 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
13. 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
14. Xeroderma pigmentosum-A Report of Three Cases from Two Families
    着色性干皮病：二家系三例报告
15. Clinical Analysis of 39 Cases with Xeroderma Pigmentosum
    着色性干皮病39例临床分析

noun

1. a rare genetic condition characterized by an eruption of exposed skin occurring in childhood and photosensitivity with severe sunburn