Reply to letter by J. H. Robbins
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00210686.pdf
Reference12 articles.
1. Arrand JE, Bone NM, Johnson RT (1989) Molecular cloning and characterisation of a mammalian excision repair gene which partially restores UV resistance to xeroderma complementation group D cells. Proc Natl Acad Sci USA (in press)
2. Fischer E, Thielmann HW, Neundörfer B, Rentsch FG, Edler L, Jung EG (1982) Xeroderma pigmentosum patients from Germany: clinical symptoms and DNA repair characteristics. Arch Dermatol Res 274:229?247
3. Fujiwara Y, Satoh Y (1985) Assignment of two Japanese xeroderma pigmentosum patients to complementation group D and their characteristics. Jpn J Cancer Res 76:162?166
4. Ichihashi M, Yamamura K, Hiramoto T, Fujiwara Y (1988) No apparent neurologic defect in a patient with xeroderma pigmentosum complementation group D. Arch Dermatol 124:256?260
5. Johnson RT, Elliott GC, Squires S, Joysey VC (1989) Lack of complementation between xeroderma pigmentosum complementation groups D and H. Hum Genet 81:203?210
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. The XPD complementation group;Mutation Research/DNA Repair;1992-03
2. Xeroderma pigmentosum complementation group H falls into complementation group D;Mutation Research/DNA Repair;1991-09
3. Localization of the xeroderma pigmentosum group B-correcting gene ERCC3 to human chromosome 2q21;Genomics;1991-08
4. Construction of a recombinant adenovirus containing the den V gene from bacteriophage T4 which can partially restore the DNA repair deficiency in xeroderma pigmentosum fibroblasts;Carcinogenesis;1991
5. Sturcture and expression of the humanXPBC/ERCC-3gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome;Nucleic Acids Research;1991
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