1. Xeroderma pigmentosum: an inherited disease with sun sensitivity, multiple cutaneous neoplasms and abnormal DNA repair;Robbins, J.H.; Kraemer, K.H.; Lutzner, M.A.; Festoff, B.W.; Coon, H.G.;Ann Intern Med,1974
2. Xeroderma pigmentosum - Cockayne syndrome complex in two patients: absence of skin tumors despite severe deficiency of DNA excision repair..7 Anm;Scott, R.J.; Itin, P.; Kleijer, W.J.; Kolb, K.; Arlett, C.F.; Mueller, H.J.;Acad Dermatol,1993
3. Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3. Am.7 Hunm Genet;Vermeulen, W.; Scott, R.J.; Rodgers, S.,1994
4. Xeroderma pigmentosum complementation group H falls into complementation group D;Vermeulen, W.; Stefanini, M.; Giliani, S.; Hoeijmakers, J.H.J.; Bootsma, D.;Mutat Res,1991
5. Molecular and cellular analysis of the DNA repair defect in a patient with xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome;Broughton, B.C.; Thompson, A.F.; Harcourt, S.A.;Am _7 Humn Genet,1995