| Nr. | Year OPEN | Title | users say | rate good | rate bad | no link | Citation |
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Fragile X syndromeAutismPervasive developmental disorderFragile X associated tremor ataxia syndromeFMR1Ovary (Insufficiency premature)Friedreich ataxiaMyotonic dystrophyTrinucleotide repeatFRAXE mental retardationFRA12A mental retardationTrinucleotide deletion| 1 | 2008 | Fragile X syndrome in Korea: a case series and a review of the literature. | 
| + | - | nl | J Korean Med Sci 23(3):470-6 (2008) |
| 2 | 1994 | Fragile X syndrome. |
| + | - | nl | Can Fam Physician 40(-):290-5 (1994) |
| 3 | 2009 | Systematic review of pharmacological treatments in fragile X syndrome. |
| + | - | nl | BMC Neurol 9(-):53 (2009) |
| 4 | 2003 | Screening for fragile X syndrome: a literature review and modelling study. |
| + | - | nl | Health Technol Assess 7(16):1-106 (2003) |
| 5 | 2004 | The fragile-X premutation: a maturing perspective. |
| + | - | nl | Am J Hum Genet 74(5):805-16 (2004) |
| 6 | 1989 | Fragile X mental retardation. |
| + | - | nl | Arch Dis Child 64(9):1223-4 (1989) |
| 7 | 2000 | Dendritic spine structural anomalies in fragile-X mental retardation syndrome. |
| + | - | nl | Cereb Cortex 10(10):1038-44 (2000) |
| 8 | 2008 | Fragile X syndrome. |
| + | - | nl | Eur J Hum Genet 16(6):666-72 (2008) |
| 9 | 2000 | Understanding the molecular basis of fragile X syndrome. |
| + | - | nl | Hum Mol Genet 9(6):901-8 (2000) |
| 10 | 1998 | The fragile X syndrome. |
| + | - | nl | J Med Genet 35(7):579-89 (1998) |
| 11 | 1993 | Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation. |
| + | - | nl | J Med Genet 30(5):410-3 (1993) |
| 12 | 1991 | Molecular genetics of fragile X: a cytogenetics viewpoint. Report of the Fifth International Symposium on X Linked Mental Retardation, Strasbourg, France, 12 to 16 August 1991 (organiser Dr J-L Mandel). |
| + | - | nl | J Med Genet 28(12):814-7 (1991) |
| 13 | 1991 | Cloning of the gene for the fragile X syndrome: implications for the clinical geneticist. |
| + | - | nl | J Med Genet 28(12):811-3 (1991) |
| 14 | 1991 | The fragile X syndrome. |
| + | - | nl | J Med Genet 28(12):809-10 (1991) |
| 15 | 1989 | Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys. |
| + | - | nl | J Med Genet 26(7):443-6 (1989) |
| 16 | 1984 | The fragile X syndrome: the patients and their chromosomes. |
| + | - | nl | J Med Genet 21(2):84-91 (1984) |
| 17 | 2006 | Local protein synthesis and spine morphogenesis: Fragile X syndrome and beyond. |
| + | - | nl | J Neurosci 26(27):7151-5 (2006) |
| 18 | 2009 | Advances in the treatment of fragile X syndrome. |
| + | - | nl | Pediatrics 123(1):378-90 (2009) |
| 19 | 1997 | Fragile X syndrome. Molecular and clinical insights and treatment issues. |
| + | - | nl | West J Med 166(2):129-37 (1997) |
| 20 | 1999 | Fragile X syndrome (review). |
| + | - | nl | Int J Mol Med 3(6):639-45 (1999) |
| 21 | 2009 | Fragile X: a family of disorders. |
| + | - | nl | Adv Pediatr 56(-):165-86 (2009) |
| 22 | 2007 | A genetic etiology of pervasive developmental disorder guides treatment. |
| + | - | nl | Am J Psychiatry 164(4):575-80 (2007) |
| 23 | 2009 | FMR1: a gene with three faces. |
| + | - | nl | Biochim Biophys Acta 1790(6):467-77 (2009) |
| 24 | 2004 | Molecular diagnosis and genetic counseling for fragile X mental retardation. |
| + | - | nl | Neurol India 52(1):36-42 (2004) |
| 25 | 2009 | Chromatin remodeling in the noncoding repeat expansion diseases. |
| + | - | nl | J Biol Chem 284(12):7413-7 (2009) |
| 26 | 2009 | Mutation spectra in fragile X syndrome induced by deletions of CGG*CCG repeats. |
| + | - | nl | J Biol Chem 284(12):7407-11 (2009) |
| 27 | 2010 | Involvement and therapeutic potential of the GABAergic system in the fragile X syndrome. |
| + | - | nl | ScientificWorldJournal 10(-):2198-206 (2010) |
