kw.\*:("Chromosome fragility")
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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
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
Fragile sites on human chromosomes: description and clinical significanceMICHELS, V. V.Mayo Clinic proceedings. 1985, Vol 60, Num 10, pp 690-696, issn 0025-6196Article
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
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
The inducible fragile site on chromosome 3BERNAR, J; FUNDERBURK, S. J; SPARKES, R. S et al.Human genetics. 1984, Vol 66, Num 4, issn 0340-6717, 373Article