All Relations between Fragile X Syndrome and fmr1
| Publication | Sentence | Publish Date | Extraction Date | Species |
|---|---|---|---|---|
| A K Gedeon, E Baker, H Robinson, M W Partington, B Gross, A Manca, B Korn, A Poustka, S Yu, G R Sutherlan. Fragile X syndrome without CCG amplification has an FMR1 deletion. Nature genetics. vol 1. issue 5. 1993-06-09. PMID:1302032. | this finding confirms that the fragile x phenotype can exist, without amplification of the ccg repeat or cytogenetic expression of the fragile x, and that fragile x syndrome is a genetically homogeneous disorder involving fmr1. | 1993-06-09 | 2023-08-11 | Not clear |
| S H Laval, H J Blair, M C Hirst, K E Davies, Y Boy. Mapping of FMR1, the gene implicated in fragile X-linked mental retardation, on the mouse X chromosome. Genomics. vol 12. issue 4. 1992-05-29. PMID:1572655. | these recombination events were used to define the position of fmr-1, the murine homologue of fmr1, which is the gene implicated in the fragile x syndrome in man, and that of dxs296h, the murine homologue of dxs296. | 1992-05-29 | 2023-08-11 | mouse |