The fragile X: a scanning electron microscope study.
| dc.contributor.author | Harrison, Christine J | |
| dc.contributor.author | Jack, E M | |
| dc.contributor.author | Allen, Terence D | |
| dc.contributor.author | Harris, R | |
| dc.date.accessioned | 2015-01-02T16:09:55Z | |
| dc.date.available | 2015-01-02T16:09:55Z | |
| dc.date.issued | 1983-08 | |
| dc.identifier.citation | The fragile X: a scanning electron microscope study. 1983, 20 (4):280-5 J Med Genet | en |
| dc.identifier.issn | 0022-2593 | |
| dc.identifier.pmid | 6684694 | |
| dc.identifier.uri | http://hdl.handle.net/10541/337763 | |
| dc.description.abstract | Scanning electron microscopy (SEM) has been used to study the fragile X chromosome. The fragile site appears as an isochromatid gap in the majority of cases, confirming light microscope (LM) observations. SEM has allowed a more precise location of the fragile site to the Xq27 . 3 region. | |
| dc.language.iso | en | en |
| dc.rights | Archived with thanks to Journal of medical genetics | en |
| dc.subject.mesh | Chromosome Mapping | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Fragile X Syndrome | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Lymphocytes | |
| dc.subject.mesh | Male | |
| dc.subject.mesh | Microscopy, Electron, Scanning | |
| dc.subject.mesh | Sex Chromosome Aberrations | |
| dc.subject.mesh | X Chromosome | |
| dc.title | The fragile X: a scanning electron microscope study. | en |
| dc.type | Article | en |
| dc.contributor.department | Department of Cell Biology, Paterson Laboratories, Christie Hospital and Holt Radium Institute, Manchester M20 9BX | en |
| dc.identifier.journal | Journal of Medical Genetics | en |
| html.description.abstract | Scanning electron microscopy (SEM) has been used to study the fragile X chromosome. The fragile site appears as an isochromatid gap in the majority of cases, confirming light microscope (LM) observations. SEM has allowed a more precise location of the fragile site to the Xq27 . 3 region. |