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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: hoeijmakers jh. Am J Hum Genet. 1995 Jan;56(1):167-74. Am J Hum Genet. 1995. PMID: 7825573 Free PMC article. Review.
DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells.
Moriwaki S, Stefanini M, Lehmann AR, Hoeijmakers JH, Robbins JH, Rapin I, Botta E, Tanganelli B, Vermeulen W, Broughton BC, Kraemer KH. Moriwaki S, et al. Among authors: hoeijmakers jh. J Invest Dermatol. 1996 Oct;107(4):647-53. doi: 10.1111/1523-1747.ep12584287. J Invest Dermatol. 1996. PMID: 8823375 Free article.
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