Authors: Busch, DB Ziffer, DW Coleman, D Wills, L McDonough, HG Jones, NJ

Citation: Db. Busch et al., Phenotype of FAECB (Facility for Automated Experiments in Cell Biology) Chinese hamster ovary mutants with minimal UV-sensitivity, MUT R-DNA R, 487(1-2), 2001, pp. 31-39

Authors: Gozukara, EM Khan, SG Metin, A Emmert, S Busch, DB Shahlavi, T Coleman, DM Miller, M Chinsomboon, N Stefanini, M Kraemer, KH

Citation: Em. Gozukara et al., A stop codon in xeroderma pigmentosum group C families in Turkey and Italy: Molecular genetic evidence for a common ancestor, J INVES DER, 117(2), 2001, pp. 197-204

Authors: Slor, H Batko, S Khan, SG Sobe, T Emmert, S Khadavi, A Frumkin, A Busch, DB Albert, RB Kraemer, KH

Citation: H. Slor et al., Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: Sun protection prolongs life, J INVES DER, 115(6), 2000, pp. 974-980

Authors: Meira, LB Graham, JM Greenberg, CR Busch, DB Doughty, ATB Ziffer, DW Coleman, DM Savre-Train, I Friedberg, EC

Citation: Lb. Meira et al., Manitoba aboriginal kindred with original cerebro-oculo-facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene, AM J HU GEN, 66(4), 2000, pp. 1221-1228

Authors: Cleaver, JE Afzal, V Feeney, L McDowell, M Sadinski, W Volpe, JPG Busch, DB Coleman, DM Ziffer, DW Yu, YJ Nagasawa, H Little, JB

Citation: Je. Cleaver et al., Increased ultraviolet sensitivity and chromosomal instability related to p53 function in the xeroderma pigmentosum variant, CANCER RES, 59(5), 1999, pp. 1102-1108