Xeroderma pigmentosum-Cockayne syndrome complex in two patients: Absence of slun tumors despite severe deficiency of DNA excision repair
- 1 November 1993
- journal article
- case report
- Published by Elsevier in Journal of the American Academy of Dermatology
- Vol. 29 (5), 883-889
- https://doi.org/10.1016/0190-9622(93)70263-s
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Cockayne syndrome: Review of 140 casesAmerican Journal of Medical Genetics, 1992
- Xeroderma pigmentosum complementation group H falls into complementation group DMutation Research/DNA Repair, 1991
- NEUROLOGICAL DISEASE IN XERODERMA PIGMENTOSUM: DOCUMENTATION OF A LATE ONSET TYPE OF THE JUVENILE ONSET FORMBrain, 1991
- Immune Function, Mutant Frequency, and Cancer Risk in the DNA Repair Defective Genodermatoses Xeroderma Pigmentosum, Cockayne's Syndrome, and TrichothiodystrophyJournal of Investigative Dermatology, 1990
- Xeroderma PigmentosumArchives of Dermatology, 1987
- Cockayne SyndromeJournal of Neuropathology and Experimental Neurology, 1985
- The Cockayne syndrome—An inherited multisystem disorder with cutaneous photosensitivity and defective repair of DNA Comparison with xeroderma pigmentosumThe American Journal of Dermatopathology, 1985
- Three complementation groups in Cockayne syndromeMutation Research, 1982
- Xeroderma pigmentosum patients from Germany: Clinical symptoms and DNA repair characteristicsArchives of Dermatological Research, 1982
- Cockayne syndromeNeurology, 1980