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