This is a preview of subscription content, log in via an institution to check access.
References
Arase S, Kozuka T, Tanaka K, Ikenaga M, Takebe H (1979) A sixth complementation group in xeroderma pigmentosum. Mutat Res 59:143–146
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
Fujiwara Y, Uehara Y, Ichihashi M, Yamamoto Y, Nishioka K (1985a) Assignment of 2 patients with xeroderma pigmentosum to complementation group E. Mutat Res 145:55–61
Fujiwara Y, Uehara Y, Ichihashi M, Nishioka K (1985b) Xeroderma pigmentosum complementation group F: more assignments and repair characteristics. Photochem Photobiol 41:629–634
Fujiwara Y, Ichihashi M, Uehara Y, Matsumoto A, Yamamoto Y, Kano Y, Tanakura Y (1985c) Xeroderma pigmentosum groups C and F: additional assignments and a review of the subjects in Japan. J Radiat Res (Tokyo) 26:443–449
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
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
Kawada A, Satoh Y, Fujiwara Y (1986) Xeroderma pigmentosum complementation group E: a case report. Photodermatology 3:233–238
Kondo S, Fukuro S, Mamada A, Kawada A, Satoh Y, Fujiwara Y (1988) Assignment of three patients with xeroderma pigmentosum to complementation group E and their characteristics. J Invest Dermatol 90:152–157
Kraemer KH, De Weerd-Kastelein EA, Robbins JH, Keijzer W, Barrett SF, Petinga RA, Bootsma D (1975) Five complementation groups in xeroderma pigmentosum. Mutat Res 33:327–340
Lafforet D, Dupuy J-M (1978) Photosensibilite et reparation de l'ADN. Possibilite d'une parente nosologique entre xeroderma pigmentosum et syndrome de Cockayne. Arch Fr Pediatr 35 [Suppl II]:65–74
Mamada A, Kondo S, Kawada A, Satoh Y, Fujiwara Y (1988) Delayed sensorineural deafness and skin carcinogenesis in a Japanese xeroderma pigmentosum group D patient. Photodermatology 5:83–91
Moshell AN, Ganges MB, Lutzner MA, Coon HF, Barrett SF, Dupuy J-M, Robbins JH (1983) A new patient with both xeroderma pigmentosum and Cockayne syndrome establishes the new xeroderma pigmentosum complementation group H. In: Friedberg EC, Bridges BA (eds) Cellular responses to DNA damage. Liss, New York, pp 209–213
Norris PG, Hawk JLM, Avery JA, Giannelli F (1988) Xeroderma pigmentosum complementation group F in a non-Japanese patient. J Am Acad Dermatol 18:1185–1188
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)
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
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
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
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
Mamada A, Kondo S, Kawada A, Satoh Y, Fujiwara Y (1988) Delayed sensoneural deafness and skin carcinogenesis in a Japanese xeroderma pigmentosum group D patient. Photodermatology 5:83–91
Mitchell DL (1988) The relative cytotoxicity of (6–4) photoproducts and cyclobutane dimers in mammalian cells. Photochem Photobiol 48:50–57
Moshell AN, Ganges MB, Lutzner MA, Coon HF, Barrett SF, Dupuy J-M, Robbins JH (1983) A new patient with both xeroderma pigmentosum and Cockayne syndrome establishes the new xeroderma pigmentosum complementation group H. In: Friedberg EC, Bridges BA (eds) Cellular responses to DNA damage. Liss, New York, pp 209–213
Paterson MC (1982) Accumulation of non-photoreactivable sites in DNA during incubation of UV-damaged xeroderma pigmentosum group A and group D cells. In: Natarajan AT, Obe B, Altmann H (eds) Progress in mutation research 4. Elsevier, Amsterdam, pp 183–192
Pawsey SA, Magnus IA, Ramsay CA, Benson PF, Giannelli F (1979) Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosum. Q J Med 48:179–210
Robbins JH, Kraemer KH, Latzner MA, Festoff BW, Coon HG (1974) Xeroderma pigmentosum an inherited disease with sun sensitivity, multiple cutaneous neoplasms, and abnormal repair. Ann Intern Med 80:221–248
Zelle B, Lohmann PHM (1979) Repair of UV-endonuclease-susceptible sites in the 7 complementation groups of xeroderma pigmentosum A through G. Mutat Res 62:363–368
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Robbins, J.H. No lack of complementation for unscheduled DNA synthesis between xeroderma pigmentosum complementation groups D and H. Hum Genet 84, 99–100 (1989). https://doi.org/10.1007/BF00210685
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00210685