Fragile X syndrome without CCG amplification has an FMR1 deletion
- 1 August 1992
- journal article
- case report
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 1 (5), 341-344
- https://doi.org/10.1038/ng0892-341
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- The common fragile site in band q27 of the human X chromosome is not coincident with the fragile XClinical Genetics, 2008
- Nomenclature guidelines for X‐linked mental retardationAmerican Journal of Medical Genetics, 1992
- Do sequences in Xq27.3 play a role in X inactivation?American Journal of Medical Genetics, 1992
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.Journal of Medical Genetics, 1991
- A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X‐linked mental retardationClinical Genetics, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeCell, 1991
- Genetic mapping of new RFLPs at Xq27–q28Genomics, 1991
- Genomic Organization of Human Centromeric Alpha Satellite DNA: Characterization of a Chromosome 17 Alpha Satellite SequenceDNA, 1987
- Clinical and cytogenetic aspects of X‐chromosome deletionsClinical Genetics, 1982