The fragile site on chromosome 3SMEETS, D. F. C. M; SCHERES, J. M. J. C; HUSTINX, T. W. J et al.Human genetics. 1984, Vol 67, Num 3, issn 0340-6717, 351Article

A new heritable fragile site on human chromosome 3MARKKANEN, A; KNUUTILA, S; DE LA CHAPELLE, A et al.Hereditas (Landskrona). 1983, Vol 99, Num 2, issn 0018-0661, 317Article

Dermatoglyphic findings in patients with fragile X-chromosomeHIRTH, L; SINGH, S; SCHILLING, S et al.Clinical genetics. 1985, Vol 27, Num 2, pp 118-121, issn 0009-9163Article

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

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

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

Hypersensitivity of xeroderma pigmentosum cells to dietary carcinogensPROTIC-S-ABLJIC, M; WHYTE, D. B; KRAEMER, K. H et al.Mutation research. 1985, Vol 145, Num 1-2, pp 89-94, issn 0027-5107Article

Idoxuridine induction of micronuclei containing the long or short arms of human chromosome 9TOMMERUP, N.Cytogenetics and cell genetics. 1984, Vol 38, Num 2, pp 92-98, issn 0301-0171Article

Expression of the fragile site Xq27 in fibroblasts. II: Evidence for negative and positive clones from heterozygous female and possible relationship between frequency and phenotypeSTEINBACH, P; BARBI, G; BAUR, S et al.Human genetics. 1983, Vol 64, Num 3, pp 279-282, issn 0340-6717Article

A search for linkage in families with fragile sitesMULLEY, J. C; NICHOLLS, C; SUTHERLAND, G. R et al.Human genetics. 1983, Vol 65, Num 1, pp 79-81, issn 0340-6717Article

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

A new familial «fragile site» on chromosome 16 (q23-24). Cytogenetic and clinical considerationsSHABTAI, F; KLAR, D; NISSIMOV, R et al.Human genetics. 1983, Vol 64, Num 3, pp 273-276, issn 0340-6717Article

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

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

Chromosome instability is associated with hypodiploid clones in myelodysplastic syndromesKNUUTILA, S; TEERENHOVI, L; BROGSTROM, G. H et al.Hereditas (Landskrona). 1984, Vol 101, Num 1, pp 19-30, issn 0018-0661Article

Additional evidence for fragile X activity in heterozygous carriersUCHIDA, I. A; FREEMAN, V. C. P; JAMRO, H et al.American journal of human genetics. 1983, Vol 35, Num 5, pp 861-868, issn 0002-9297Article

Congenital ocular motor apraxiaNEETENS, A; RUBBENS, M. C.Bulletin de la Société belge d'ophtalmologie. 1983, Vol 203, pp 71-74, issn 0081-0746Article