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Arlett, C.F.
( C.F. Arlett)
2 Most Recent Publications
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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.
(Article)
Broughton, B.C. Thompson, A.F. Arlett, C.F. Lehmann, A.R. Harcourt, S.A. Vermeulen, W. Hoeijmakers, J.H.J. Botta, E. Stefanini, M. King, M.D. Weber, C.A. Cole, J. |
1995-01-01
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Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.
(Article)
Vermeulen, W. Scott, R.J. Potger, S. Müller, H.J. Cole, J. Arlett, C.F. Kleijer, W.J. Bootsma, D. Hoeijmakers, J.H.J. Weeda, G. |
1994-01-01
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