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Les syndromes d'instabilité chromosomique = Chromosomal instability syndromesGERMAIN, D; BERNHEIM, A.La Semaine des hôpitaux de Paris. 1983, Vol 59, Num 44, pp 3065-3079, issn 0037-1777Article

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

Chromosome fragility in Alzheimer's diseaseSMITH, A; BROE, G. A; WILLIAMSON, M et al.Clinical genetics. 1984, Vol 25, Num 5, pp 416-421, issn 0009-9163Article

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

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

Increased chromosomal instability in lymphocytes from elderly humansDUTKOWSKI, R. T; LESH, R; STAIANO-COICO, L et al.Mutation research. 1985, Vol 149, Num 3, pp 505-512, issn 0027-5107Article

Diagnosis of the fragile X syndrome (Martin-Bell syndrome): clinical findings in 27 males with the fragile site at Xq28NIELSEN, K. B.Journal of mental deficiency research. 1983, Vol 27, Num 3, pp 211-226, issn 0022-264XArticle

Folic acid metabolism in a patient with fragile XBRONDUM NIELSEN, K; TOMMERUP, N; FRIIS, B et al.Clinical genetics. 1983, Vol 24, Num 3, pp 153-155, issn 0009-9163Article

On the nature of folic-acid-sensitive fragile sites in human chromosomes: an hypothesisKRUMDIECK, C. L; HOWARD-PEEBLES, P. N.American journal of medical genetics. 1983, Vol 16, Num 1, pp 23-28, issn 0148-7299Article

Tables for the cytogenetic study of fragile X chromosomes for diagnostic purposesDE ARCE, M. A.Clinical genetics. 1983, Vol 24, Num 5, pp 320-323, issn 0009-9163Article

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

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

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