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Perturbed replication induced genome wide or at common fragile sites is differently managed in the absence of WRNMURFUNI, Ivana; DE SANTIS, Anita; FEDERICO, Maurizio et al.Carcinogenesis (New York. Print). 2012, Vol 33, Num 9, pp 1655-1663, issn 0143-3334, 9 p.Article

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Le syndrome de Werner = Werner's syndromeRUTO, F; LABEILLE, B; GONTIER, M. F et al.Les Nouvelles dermatologiques. 1992, Vol 11, Num 5, pp 288-289, issn 0752-5370Conference Paper

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Fragile X SyndromeWALLACE HAYES, Eriel; MATALON, Reuben.Pediatrics (Evanston). 2009, Vol 124, Num 2, pp 790-792, issn 0031-4005, 3 p.Article

Fragile sites and human diseaseDEBACKER, Kim; KOOY, R. Frank.Human molecular genetics (Print). 2007, Vol 16, issn 0964-6906, R150-R158, NS2Article

Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported onesMRASEK, Kristin; SCHODER, Christiane; TEICHMANN, Anne-Christin et al.International journal of oncology. 2010, Vol 36, Num 4, pp 929-940, issn 1019-6439, 12 p.Article

Fragile X premutation with atypical symptoms at onsetCELLINI, Elena; FORLEO, Paolo; GINESTRONI, Andrea et al.Archives of neurology (Chicago). 2006, Vol 63, Num 8, pp 1135-1138, issn 0003-9942, 4 p.Article

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Fragile X syndrome : An epigenetic diseaseSTOYANOVA, Violeta; HOOGEVEEN, André T.The molecular basis of fragile X syndrome. 2005, pp 1-16, isbn 81-7736-257-7, 1Vol, 16 p.Book Chapter

U rich RNA binding sites of the fragile X mental retardation proteinTOTH, M.The molecular basis of fragile X syndrome. 2005, pp 43-50, isbn 81-7736-257-7, 1Vol, 8 p.Book Chapter

When Fragile X meets Rho GTPase signalling : Novel insights from fly CYFIPSCHENCK, Annette; GIANGRANDE, Angela.The molecular basis of fragile X syndrome. 2005, pp 81-116, isbn 81-7736-257-7, 1Vol, 36 p.Book Chapter