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Lack of FMR3 expression in a male with non-syndromic mental retardation and a microdeletion immediately distal to FRAXE CCG repeatSANTOS-REBOUCAS, Cintia Barros; ABDALLA, Claudia Bueno; FULLSTON, Tod et al.Neuroscience letters. 2006, Vol 397, Num 3, pp 245-248, issn 0304-3940, 4 p.Article

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Population cytogenetics of folate-sensitive fragile sites. II: Autosomal rare fragile sitesKAHKONEN, M; TENGSTROM, C; ALITALO, T et al.Human genetics. 1989, Vol 82, Num 1, pp 3-8, issn 0340-6717, 6 p.Article

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

Chromosomal studies on sphaerodactyl lizards of genera Gonatodes and Coleodactylus (Squamata, Gekkonidae) using differential staining and fragile sites analysesDOS SANTOS, R. M. L; BERTOLOTTO, C. E. V; PELLEGRINO, K. C. M et al.Cytogenetic and genome research. 2003, Vol 103, Num 1-2, pp 128-134, issn 1424-8581, 7 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

Impaired replication dynamics at the FRA3B common fragile sitePALAKODETI, Aparna; LUCAS, Isabelle; YANWEN JIANG et al.Human molecular genetics (Print). 2010, Vol 19, Num 1, pp 99-110, issn 0964-6906, 12 p.Article

Common fragile sites: mechanisms of instability revisitedDEBATISSE, Michelle; LE TALLEC, Benoît; LETESSIER, Anne et al.Trends in genetics (Regular ed.). 2012, Vol 28, Num 1, pp 22-32, issn 0168-9525, 11 p.Article

SMC1 involvement in fragile site expressionMUSIO, Antonio; MONTAGNA, Cristina; RIED, Thomas et al.Human molecular genetics (Print). 2005, Vol 14, Num 4, pp 525-533, issn 0964-6906, 9 p.Article

Evidence of chromosomal fragile sites in schizophrenic patientsGAROFALO, G; RAGUSA, R. M; ARGIOLAS, A et al.Annales de génétique (Paris). 1993, Vol 36, Num 2, pp 132-135, issn 0003-3995Article

The most common fragile site in man is 3p14SMEETS, D. F. C. M; SCHERES, J. M. J. C; HUSTINX, T. W. J et al.Human genetics. 1986, Vol 72, Num 3, pp 215-220, issn 0340-6717Article

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Rare and polymorphic fragile sites and cancerHECHT, F.Cancer genetics and cytogenetics. 1988, Vol 34, Num 2, pp 195-199, issn 0165-4608Article

Population cytogenetics of rare fragile sites in JapanTAKAHASHI, E; HORI, T; MURATA, M et al.Human genetics. 1988, Vol 78, Num 2, pp 121-126, issn 0340-6717Article

Expression of fragile sites in childhood acute lymphoblastic leukemia patients and normal controlsNAGESH RAO, P; HEEREMA, N. A; PALMER, C. G et al.Human genetics. 1988, Vol 79, Num 4, pp 329-334, issn 0340-6717Article

Fragile site induction by aphidicolin may be increased in parents of neuroblastoma patientsVERNOLE, P; TEDESCHI, B; NICOLETTI, B et al.Cancer genetics and cytogenetics. 1990, Vol 50, Num 1, pp 35-44, issn 0165-4608, 10 p.Article

Arabinofuranosyl nucleosides induce common fragile sitesLEONARD, J. C; LEONARD, R. C; THOMPSON, K. H et al.Human genetics. 1988, Vol 79, Num 2, pp 157-162, issn 0340-6717Article

Cloning of genetically tagged chromosome break sequences reveals new fragile sites at 6p21 and 13q22FECHTER, Anne; BUETTEL, Isabel; KUEHNEL, Elisabeth et al.International journal of cancer. 2007, Vol 120, Num 11, pp 2359-2367, issn 0020-7136, 9 p.Article

RORA, a large common fragile site gene, is involved in cellular stress responseZHU, Y; MCAVOY, S; KUHN, R et al.Oncogene (Basingstoke). 2006, Vol 25, Num 20, pp 2901-2908, issn 0950-9232, 8 p.Article

DNA copy number amplification profiling of human neoplasmsMYLLYKANGAS, S; HIMBERG, J; BÖHLING, T et al.Oncogene (Basingstoke). 2006, Vol 25, Num 55, pp 7324-7332, issn 0950-9232, 9 p.Article