Back to Search
Start Over
Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplification
- Source :
- Journal of Medical Genetics. September, 2001, Vol. 38 Issue 9, 624
- Publication Year :
- 2001
-
Abstract
- EDITOR--Fragile X syndrome is the most common chromosomal cause of inherited mental retardation. At the chromosome level, this syndrome is characterised by the presence of a fragile site at Xq27.3. [...]
- Subjects :
- Fragile X syndrome -- Research
Genetic disorders -- Research
Health
Subjects
Details
- Language :
- English
- ISSN :
- 00222593
- Volume :
- 38
- Issue :
- 9
- Database :
- Gale General OneFile
- Journal :
- Journal of Medical Genetics
- Publication Type :
- Periodical
- Accession number :
- edsgcl.78839852