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Results: 1-4 |
Results: 4

Authors: Vermeulen, W Rademakers, S Jaspers, NGJ Appeldoorn, E Raams, A Klein, B Kleijer, WJ Hansen, LK Hoeijmakers, JHJ
Citation: W. Vermeulen et al., A temperature-sensitive disorder in basal transcription and DNA repair in humans, NAT GENET, 27(3), 2001, pp. 299-303

Authors: Zafeiriou, DI Thorel, F Andreou, A Kleijer, WJ Raams, A Garritsen, VH Gombakis, N Jaspers, NGJ Clarkson, SG
Citation: Di. Zafeiriou et al., Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy, PEDIAT RES, 49(3), 2001, pp. 407-412

Authors: Graham, JM Anyane-Yeboa, K Raams, A Appeldoorn, E Kleijer, WJ Garritsen, VH Busch, D Edersheim, TG Jaspers, NGJ
Citation: Jm. Graham et al., Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy, AM J HU GEN, 69(2), 2001, pp. 291-300

Authors: Stewart, GS Maser, RS Stankovic, T Bressan, DA Kaplan, MI Jaspers, NGJ Raams, A Byrd, PJ Petrini, JHJ Taylor, AMR
Citation: Gs. Stewart et al., The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder, CELL, 99(6), 1999, pp. 577-587
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