Authors: MALLERY DL TANGANELLI B COLELLA S STEINGRIMSDOTTIR H VANGOOL AJ TROELSTRA C STEFANINI M LEHMANN AR

Citation: Dl. Mallery et al., MOLECULAR ANALYSIS OF MUTATIONS IN THE CSB (ERCC6) GENE IN PATIENTS WITH COCKAYNE-SYNDROME, American journal of human genetics, 62(1), 1998, pp. 77-85

Authors: MORIWAKI SI STEFANINI M LEHMANN AR HOEIJMAKERS JHJ ROBBINS JH RAPIN I BOTTA E TANGANELLI B VERMEULEN W BROUGHTON BC KRAEMER KH

Citation: Si. Moriwaki et al., DNA-REPAIR AND ULTRAVIOLET MUTAGENESIS IN CELLS FROM A NEW PATIENT WITH XERODERMA-PIGMENTOSUM GROUP-G AND COCKAYNE-SYNDROME RESEMBLE XERODERMA-PIGMENTOSUM CELLS, Journal of investigative dermatology, 107(4), 1996, pp. 647-653

Authors: STEFANINI M TANGANELLI B PANZARASA C RIBONI R BOTTA E

Citation: M. Stefanini et al., IDENTIFICATION OF MAMMALIAN MUTANTS DEFECTIVE IN NUCLEOTIDE-EXCISION REPAIR, Journal of cellular biochemistry, 1995, pp. 283-283

Authors: CARREAU M EVENO E QUILLIET X CHEVALIERLAGENTE O BENOIT A TANGANELLI B STEFANINI M VERMEULEN W HOEIJMAKERS JHJ SARASIN A MEZZINA M

Citation: M. Carreau et al., DEVELOPMENT OF A NEW EASY COMPLEMENTATION ASSAY FOR DNA-REPAIR DEFICIENT HUMAN SYNDROMES USING CLONED REPAIR GENES, Carcinogenesis, 16(5), 1995, pp. 1003-1009