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  1. 1
    Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes

    Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes von Carreau, Madeleine, Eveno, Eric, Quilliet, Xavier, Chevalier-Lagente, Odile, Benoit, Annie, Tanganelli, Bianca, Stefanini, Miria, Vermeulen, Wim, Hoeijmakers, Jan H.J., Sarasin, Alian, Mezzina, Mauro

    Veröffentlicht in Carcinogenesis (New York)

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  2. 2
    Molecular Analysis of Mutations in the CSB(ERCC6) Gene in Patients with Cockayne Syndrome

    Molecular Analysis of Mutations in the CSB(ERCC6) Gene in Patients with Cockayne Syndrome von Mallery, Donna L., Tanganelli, Bianca, Colella, Stefano, Steingrimsdottir, Herdis, van Gool, Alain J., Troelstra, Christine, Stefanini, Miria, Lehmann, Alan R.


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  3. 3
    DNA Repair and Ultraviolet Mutagenesis in Cells From a New Patient With Xeroderma Pigmentosum Group G and Cockayne Syndrome Resemble Xeroderma Pigmentosum Cells

    DNA Repair and Ultraviolet Mutagenesis in Cells From a New Patient With Xeroderma Pigmentosum Group G and Cockayne Syndrome Resemble Xeroderma Pigmentosum Cells von Moriwaki, Shin-Ichi, Stafanim, Miria, Lehmann, Alan R., Hoeijmakers, Jan H.J., Robbins, Jay H., Rapin, Isablle, Botta, Elena, Tanganelli, Bianca, Vermeulen, Wim, Broughton, Benard C., Kraemer, Kenneth H.


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