Fragile X syndrome: recognition in young childrenSIMKO, A; HORNSTEIN, L; SOUKUP, S et al.Pediatrics (Evanston). 1989, Vol 83, Num 4, pp 547-552, issn 0031-4005, 6 p.Article

The role of recombination in the evolvement of the fragile X mutationSCHAAP, T.Human genetics. 1989, Vol 82, Num 1, pp 79-81, issn 0340-6717, 3 p.Article

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

Invited editorial : the fragile X : progress toward solving the puzzleTED BROWN, W.American journal of human genetics. 1990, Vol 47, Num 2, pp 175-180, issn 0002-9297, 6 p.Article

Recombination and the fragile XSUTHERS, G. K; SUTHERLAND, G. R.Human genetics. 1990, Vol 85, Num 1, pp 141-142, issn 0340-6717, 2 p.Article

Fragile X syndrome : Symposium : Neurology-IIPHILLIPS, J. P; WILSON, G. A.Indian journal of pediatrics. 1998, Vol 65, Num 2, pp 181-191, issn 0019-5456Article

Management of chronic painHELME, R. D; KATZ, B.Medical journal of Australia. 1993, Vol 158, Num 7, pp 478-481, issn 0025-729XArticle

Fragile X syndrome : the most common cause of familial intellectual handicapSUTHERLAND, G. R; MULLEY, J. C; RICHARDS, R. I et al.Medical journal of Australia. 1993, Vol 158, Num 7, pp 482-485, issn 0025-729XArticle

Periventricular heterotopia in fragile X syndromeMORO, F; PISANO, T; GUERRINI, R et al.Neurology. 2006, Vol 67, Num 4, pp 713-715, issn 0028-3878, 3 p.Article

FMRP (Fragile X Mental Retardation Protein) interacting proteins : From a complex to a pathwayCASTETS, Made; MANDEL, Jean-Louis; BARDONI, Barbara et al.The molecular basis of fragile X syndrome. 2005, pp 117-127, isbn 81-7736-257-7, 1Vol, 11 p.Book Chapter

The means shape the ends : The localization and function of FMRPANTAR, Laura N; BASSELL, Gary J.The molecular basis of fragile X syndrome. 2005, pp 171-199, isbn 81-7736-257-7, 1Vol, 29 p.Book Chapter

Fragile x syndrome phenotype with normal FMR1 gene studiesCLARKE, Nigel F; MOWAT, David; KOOY, R. Frank et al.American journal of medical genetics. 2004, Vol 129A, Num 3, pp 326-328, issn 0148-7299, 3 p.Article

Expansion to full mutation of a FMR1 intermediate allele over two generationsTERRACCIANO, Alessandra; POMPONI, Maria Grazia; MARINO, Grazia Maria et al.European journal of human genetics. 2004, Vol 12, Num 4, pp 333-336, issn 1018-4813, 4 p.Article

Understanding fragile X syndrome: insights from animal modelsBAKKER, C. E; OOSTRA, B. A.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 111-123, issn 1424-8581, 13 p.Article

An atypical case of fragile X syndrome caused by a deletion that includes the FMRI geneQUAN, F; ZONANA, J; GUNTER, K et al.American journal of human genetics. 1995, Vol 56, Num 5, pp 1042-1051, issn 0002-9297Article

L'autisme et les enfants porteurs d'un X fragile = Autism and the fragile X syndromeSIBERTIN BLANC, D; D'ANGELO, N; LECAVELIER DES ETANGS, N et al.Annales de pédiatrie (Paris). 1993, Vol 40, Num 9, pp 565-572, issn 0066-2097Article

Prenatal diagnosis of fragile X syndromeHIRST, M; KNIGHT, S; XIAO-HUA DING et al.Lancet (British edition). 1991, Vol 338, Num 8772, pp 956-958, issn 0140-6736Article

Ocular anomalies in fragile X syndromeMAINO, D. M; SCHLANGE, D; MAINO, J. H et al.Journal of the American Optometric Association. 1990, Vol 61, Num 4, pp 316-323, issn 0003-0244, 8 p.Article

Fragile X premutation with atypical symptoms at onsetCELLINI, Elena; FORLEO, Paolo; GINESTRONI, Andrea et al.Archives of neurology (Chicago). 2006, Vol 63, Num 8, pp 1135-1138, issn 0003-9942, 4 p.Article

Syndrome de l'X fragile : comment en faire un diagnostic précoce? = X fragile syndrome; how to make a precocious diagnosticGERARD-BLANLUET, Marion.La Revue du praticien (Paris). 2005, Vol 55, Num 1, pp 7-12, issn 0035-2640, 6 p.Article

Fragile X syndrome : An epigenetic diseaseSTOYANOVA, Violeta; HOOGEVEEN, André T.The molecular basis of fragile X syndrome. 2005, pp 1-16, isbn 81-7736-257-7, 1Vol, 16 p.Book Chapter

U rich RNA binding sites of the fragile X mental retardation proteinTOTH, M.The molecular basis of fragile X syndrome. 2005, pp 43-50, isbn 81-7736-257-7, 1Vol, 8 p.Book Chapter

When Fragile X meets Rho GTPase signalling : Novel insights from fly CYFIPSCHENCK, Annette; GIANGRANDE, Angela.The molecular basis of fragile X syndrome. 2005, pp 81-116, isbn 81-7736-257-7, 1Vol, 36 p.Book Chapter

The fragile X premutation presenting as postprandial hypotensionPUGLIESE, P; ANNESI, G; QUATTRONE, A et al.Neurology. 2004, Vol 63, Num 11, pp 2188-2189, issn 0028-3878, 2 p.Article

Of mice and the fragile X syndromeKOOY, R. Frank.Trends in genetics (Regular ed.). 2003, Vol 19, Num 3, pp 148-154, issn 0168-9525, 7 p.Article