Authors:
Kraakman-van der Zwet, M
Overkamp, WJI
Jaspers, NGJ
Natarajan, AT
Lohman, PHM
Zdzienicka, MZ
Citation: M. Kraakman-van Der Zwet et al., Complementation of chromosomal aberrations in AT/NBS hybrids: inadequacy of RDS as an endpoint in complementation studies with immortal NBS cells, MUT R-DNA R, 485(3), 2001, pp. 177-185
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:
Petit-Frere, C
Capulas, E
Lowe, JE
Koulu, L
Marttila, RJ
Jaspers, NGJ
Clingen, PH
Green, MHL
Arlett, CF
Citation: C. Petit-frere et al., Ultraviolet-B-induced apoptosis and cytokine release in xeroderma pigmentosum keratinocytes, J INVES DER, 115(4), 2000, pp. 687-693
Authors:
Kraakman-van der Zwet, M
Overkamp, WJI
Friedl, AA
Klein, B
Verhaegh, GWCT
Jaspers, NGJ
Midro, AT
Eckardt-Schupp, F
Lohman, PHM
Zdzienicka, MZ
Citation: M. Kraakman-van Der Zwet et al., Immortalization and characterization of Nijmegen Breakage Syndrome fibroblasts, MUT R-DNA R, 434(1), 1999, pp. 17-27
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