Fragile X testing in a diagnostic cytogenetics laboratory.
- 1 July 1989
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 26 (7) , 439-442
- https://doi.org/10.1136/jmg.26.7.439
Abstract
Chromosome results obtained from 1012 patients referred with developmental delay without known cause within the three years 1985 to 1987 are reported. G banding analysis and assessment of 70 cells for fragile X gave abnormal results in 84 cases: fragile X in 31 patients and other abnormalities in 53 patients. A further 16 sibs expressing the fragile X were detected in family studies originating from the 31 index cases. This yield justifies continuation of procedures which detect both fragile X and subtle chromosomal abnormalities in these patients.This publication has 8 references indexed in Scilit:
- The frequency of the fragile X chromosome among schoolchildren in Coventry.Journal of Medical Genetics, 1986
- Preventive Screening for the Fragile X SyndromeNew England Journal of Medicine, 1986
- Normal male carriers in the fra(X) form of X‐linked mental retardation (Martin—Bell syndrome)American Journal of Medical Genetics, 1986
- Detection of the fragile X chromosome and other fragile sitesClinical Genetics, 1985
- The marker (X) syndrome: a cytogenetic and genetic analysisAnnals of Human Genetics, 1984
- Tables for the cytogenetic study of fragile X chromosomes for diagnostic purposes.1983
- DE NOVO STRUCTURAL REARRANGEMENTS: IMPLICATIONS FOR PRENATAL DIAGNOSISPublished by Elsevier ,1982
- Fragile sites on human chromosomesPathology, 1981