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Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.
Broughton BC, Thompson AF, Harcourt SA, Vermeulen W, Hoeijmakers JH, Botta E, Stefanini M, King MD, Weber CA, Cole J, et al. Broughton BC, et al. Among authors: cole j. Am J Hum Genet. 1995 Jan;56(1):167-74. Am J Hum Genet. 1995. PMID: 7825573 Free PMC article. Review.
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