| Literature DB >> 4042405 |
D Abuelo, K Castree, S Pueschel, T Padre-Mendoza, K Zolnierz.
Abstract
Because of the ambiguities in diagnosing carriers of the fragile X syndrome, we studied thirty-six normal females to determine whether the fragile site at Xq27 can be seen in noncarrier females and at what frequency. A fragile site at Xq27 was identified in one out of thirty-six females, occurring at a frequency of 0.5% in her peripheral lymphocytes. We conclude that the fragile Xq27 site occurs only rarely in noncarrier females and that each laboratory should determine its own baseline frequencies of fragile X in order to most accurately distinguish between normal and carrier women.Entities:
Mesh:
Year: 1985 PMID: 4042405 DOI: 10.1111/j.1399-0004.1985.tb00366.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438