| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Hirst MC | |
| P2860 | cites work | Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox | Q28235115 |
| Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome | Q33676149 | ||
| Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate | Q36756225 | ||
| Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus | Q37600444 | ||
| Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation | Q39111532 | ||
| Length of uninterrupted CGG repeats determines instability in the FMR1 gene | Q39111985 | ||
| Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I. | Q41516217 | ||
| Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington disease. | Q45288509 | ||
| A novel repeat structure at the myotonic dystrophy locus in a 37 repeat allele with unexpectedly high stability | Q46343295 | ||
| Apparent regression of the CGG repeat in FMR1 to an allele of normal size | Q47366806 | ||
| Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population. | Q52024857 | ||
| Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles. | Q52025538 | ||
| Frequency and stability of the fragile X premutation. | Q52028259 | ||
| CAG repeat length variation in sperm from a patient with Kennedy's disease | Q72253594 | ||
| Precursor arrays for triplet repeat expansion at the fragile X locus | Q72449243 | ||
| Haplotype analysis at the FRAXA locus in the Japanese population | Q72761290 | ||
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 761-763 | |
| P577 | publication date | 1995-10-01 | |
| P1433 | published in | Journal of Medical Genetics | Q14640281 |
| P1476 | title | FMR1 triplet arrays: paying the price for perfection | |
| P478 | volume | 32 |
| Q34665039 | Cloned human FMR1 trinucleotide repeats exhibit a length- and orientation-dependent instability suggestive of in vivo lagging strand secondary structure |
| Q24793185 | Fragile X (CGG)n repeats induce a transcriptional repression in cis upon a linked promoter: evidence for a chromatin mediated effect |
| Q41579814 | Screening for fragile X syndrome: information needs for health planners |
| Q71578932 | Significance of linkage disequilibrium between the fragile X locus and its flanking markers |
| Q74809876 | The fragile X syndrome |
| Q73013123 | X-linked mental retardation |
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