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Folic acid sensitive fragile sites are not limited to the human karyotype. Demonstration of nonrandom gaps and breaks in the Persian vole Ellobius lutescens Th. inducible by methotrexate, fluorodeoxyuridine, and aphidicolinDJALALI, M; BARBI, G; STEINBACH, P et al.Human genetics. 1985, Vol 70, Num 2, pp 183-185, issn 0340-6717Article

Rare fragile sitesSUTHERLAND, G. R.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 77-84, issn 1424-8581, 8 p.Article

Common fragile sitesARIT, M. F; CASPER, A. M; GLOVER, T. W et al.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 92-100, issn 1424-8581, 9 p.Article

Effect of folic acid treatment in the fragile X syndromeGUSTAVSON, K.-H; DAHLBOM, K; FLOOD, A et al.Clinical genetics. 1985, Vol 27, Num 5, pp 463-467, issn 0009-9163Article

Of fragile sites and cancer chromosome breakpointsHECHT, F; SANDBERG, A. A.Cancer genetics and cytogenetics. 1988, Vol 31, Num 1, pp 1-3, issn 0165-4608Article

Nature of distamycin A-inducible fragile sitesHORI, T; TAKAHASHI, E; MURATA, M et al.Cancer genetics and cytogenetics. 1988, Vol 34, Num 2, pp 189-194, issn 0165-4608Article

Forgotten fragile sites and related phenomenaSUTHERLAND, G. R; BAKER, E.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 89-91, issn 1424-8581, 3 p.Article

Segregation analysis with uncertain ascertainment: application to Fanconi anemiaROGATKO, A; AUERBACH, A. D.American journal of human genetics. 1988, Vol 42, Num 6, pp 889-897, issn 0002-9297Article

Reversing the Effects of Fragile X SyndromeOGREN, Marilee P; LOMBROSO, Paul J.Journal of the American Academy of Child and Adolescent Psychiatry. 2008, Vol 47, Num 8, pp 863-867, issn 0890-8567, 5 p.Article

How common are common fragile sites in humans: interindividual variation in the distribution of aphidicolin-induced fragile sitesDENISON, S. R; SIMPER, R. K; GREENBAUM, I. F et al.Cytogenetic and genome research. 2003, Vol 101, Num 1, pp 8-16, issn 1424-8581, 9 p.Article

The rare human fragile site 16BFELBOR, U; FEICHTINGER, W; SCHMID, M et al.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 85-88, issn 1424-8581, 4 p.Article

Genetic instability as the primary cause of human agingSTREHLER, B. L.Experimental gerontology. 1986, Vol 21, Num 4-5, pp 283-319, issn 0531-5565Article

The fragile-X premutation: A maturing perspectiveHAGERMAN, Paul J; HAGERMAN, Randi J.American journal of human genetics. 2004, Vol 74, Num 5, pp 805-816, issn 0002-9297, 12 p.Article

Variability in expression of common fragile sites : in search of a new criterionJORDAN, D. K; BURNS, T. L; DIVELBISS, J. E et al.Human genetics. 1990, Vol 85, Num 5, pp 462-466, issn 0340-6717, 5 p.Article

Chromosomal fragile sites and cancer-specific breakpoints ― A moderating viewpointLE BEAU, M. M.Cancer genetics and cytogenetics. 1988, Vol 31, Num 1, pp 55-61, issn 0165-4608Article

Frequency of tri- and multiradial configurations in fragile X chromosomesSUBRT, I; STIRSKA, K.Human genetics. 1988, Vol 78, Num 2, pp 196-197, issn 0340-6717Article

Etude de la fragilité chromosomique chez des malades atteints de maladies viralesXIAO BAI; ZHOU XIANTING; WANG ANQI et al.Yíchuán xuébào. 1986, Vol 13, Num 3, pp 232-237, issn 0379-4172Article

Refractive errors in the fragile-X syndromeFLOOD, A; SANNER, G.Acta paediatrica scandinavica. 1985, Vol 74, Num 6, issn 0001-656X, 974Article

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

The distribution of MspI-induced breaks in human lymphocyte chromosomes and its relationship to common fragile sitesPORFIRIO, B; TEDESCHI, B; VERNOLE, P et al.Mutation research. 1989, Vol 213, Num 2, pp 117-124, issn 0027-5107Article

Genetic mapping of DNA segments relative to the locus for the fragile-X-syndrome at Xq 27.3MULLIGAN, L. M; PHILLIPS, M. A; FORSTER-GIBSON, C. J et al.American journal of human genetics. 1985, Vol 37, Num 3, pp 463-472, issn 0002-9297Article

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

Enhanced sensitivity of lymphoblastoid cells from individuals carrying the mutation for the fragile X syndrome to the clastogenic effects of FUdRDUNCAN, A. M. V.Mutation research. 1986, Vol 173, Num 3, pp 201-205, issn 0027-5107Article

Folic acid blinded trial in identical twins with fragile X-syndromeROSENBLATT, D. S; DUSCHENES, E. A; HELLSTROM, F. V et al.American journal of human genetics. 1985, Vol 37, Num 3, pp 543-552, issn 0002-9297Article

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