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Authors: OTRIN VR KURAOKA I NARDO T MCLENIGAN M EKER APM STEFANINI M LEVINE AS WOOD RD
Citation: Vr. Otrin et al., RELATIONSHIP OF THE XERODERMA-PIGMENTOSUM GROUP-E DNA-REPAIR DEFECT TO THE CHROMATIN AND DNA-BINDING PROTEINS UV-DDB AND REPLICATION PROTEIN-A, Molecular and cellular biology, 18(6), 1998, pp. 3182-3190

Authors: BOTTA E NARDO T BROUGHTON BC MARINONI S LEHMANN AR STEFANINI M
Citation: E. Botta et al., ANALYSIS OF MUTATIONS IN THE XPD GENE IN ITALIAN PATIENTS WITH TRICHOTHIODYSTROPHY - SITE OF MUTATION CORRELATES WITH REPAIR DEFICIENCY, BUT GENE DOSAGE APPEARS TO DETERMINE CLINICAL SEVERITY, American journal of human genetics, 63(4), 1998, pp. 1036-1048

Authors: MONDELLO C RIBONI R NARDO T NUZZO F
Citation: C. Mondello et al., GROWTH-CHARACTERISTICS, KARYOTYPE CHANGES AND TELOMERE LENGTH VARIATIONS DURING IN-VITRO AGING OF HUMAN FIBROBLAST CLONES, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 371-371

Authors: RIBONI R CASATI A NARDO T ZACCARO E FERRETTI L NUZZO F MONDELLO C
Citation: R. Riboni et al., TELOMERIC FUSIONS IN CULTURED HUMAN FIBROBLASTS AS A SOURCE OF GENOMIC INSTABILITY, Cancer genetics and cytogenetics, 95(2), 1997, pp. 130-136

Authors: TUPLER R MARSEGLIA GL STEFANINI M PROSPERI E CHESSA L NARDO T MARCHI A MARASCHIO P
Citation: R. Tupler et al., A VARIANT OF THE NIJMEGEN BREAKAGE SYNDROME WITH UNUSUAL CYTOGENETIC FEATURES AND INTERMEDIATE CELLULAR RADIOSENSITIVITY, Journal of Medical Genetics, 34(3), 1997, pp. 196-202

Authors: MONDELLO C RIBONI R CASATI A NARDO T NUZZO F
Citation: C. Mondello et al., CHROMOSOMAL INSTABILITY AND TELOMERE LENGTH VARIATIONS DURING THE LIFE-SPAN OF HUMAN FIBROBLAST CLONES, Experimental cell research, 236(2), 1997, pp. 385-396

Authors: STEFANINI M FAWCETT H BOTTA E NARDO T LEHMANN AR
Citation: M. Stefanini et al., GENETIC-ANALYSIS OF 22 PATIENTS WITH COCKAYNE-SYNDROME, Human genetics, 97(4), 1996, pp. 418-423

Authors: MONDELLO C NARDO T GILIANI S ARRAND JE WEBER CA LEHMANN AR NUZZO F STEFANINI M
Citation: C. Mondello et al., MOLECULAR ANALYSIS OF THE XP-D GENE IN ITALIAN FAMILIES WITH PATIENTSAFFECTED BY TRICHOTHIODYSTROPHY AND XERODERMA-PIGMENTOSUM GROUP-D, MUTATION RESEARCH, 314(2), 1994, pp. 159-165

Authors: STEFANINI M LAGOMARSINI P GILIANI S NARDO T BOTTA E PESERICO A KLEIJER WJ LEHMANN AR SARASIN A
Citation: M. Stefanini et al., GENETIC-HETEROGENEITY OF THE EXCISION REPAIR DEFECT ASSOCIATED WITH TRICHOTHIODYSTROPHY, Carcinogenesis, 14(6), 1993, pp. 1101-1105

Authors: STEFANINI M VERMEULEN W WEEDA G GILIANI S NARDO T MEZZINA M SARASIN A HARPER JI ARLETT CF HOEIJMAKERS JHJ LEHMANN AR
Citation: M. Stefanini et al., A NEW NUCLEOTIDE-EXCISION-REPAIR GENE ASSOCIATED WITH THE DISORDER TRICHOTHIODYSTROPHY, American journal of human genetics, 53(4), 1993, pp. 817-821
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