Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1979.tb00982.x/fullpdf
Reference23 articles.
1. A sixth complementation group in xeroderma pigmentosum;Arase;Mut. Res.,1979
2. Different inherited levels of DNA repair replication in xeroderma pigmentosum cell strains after exposure to ultraviolet irradiation;Bootsma;Mut. Res.,1970
3. Ultraviolet-stimulated thymidine incorporation in xeroderma pigmentosum lymphocytes;Burk;J. Lab. clin. Med.,1971
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4. The Comet Assay as a Repair Test for Prenatal Diagnosis of Xeroderma Pigmentosum and Trichothiodystrophy;Journal of Investigative Dermatology;1997-02
5. Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy: sun sensitivity, DNA repair defects and skin cancer;Genetic Predisposition to Cancer;1996
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