| Literature DB >> 9050914 |
R Willemsen1, A Smits, S Mohkamsing, H van Beerendonk, A de Haan, B de Vries, A van den Ouweland, E Sistermans, H Galjaard, B A Oostra.
Abstract
To date, the identification of patients and carriers of the fragile X syndrome has been carried out by DNA analysis by means of the polymerase chain reaction and Southern blot analysis. This direct DNA analysis allows both the size of the CGG repeat and methylation status of the FMR1 gene to be determined. We have recently presented a rapid antibody test on blood smears based on the presence of FMRP, the protein product of the FMR1 gene, in lymphocytes from normal individuals and the absence of FMRP in lymphocytes from patients. Here, we have tested the diagnostic value of this new technique by studying FMRP expression in 173 blood smears from normal individuals and fragile X patients. The diagnostic power of the antibody test is "perfect" for males, whereas the results are less specific for females.Entities:
Mesh：
Substances：
Year: 1997 PMID： 9050914 DOI： 10.1007/s004390050363
Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132