Literature DB >> 4042405

Frequency of fragile X chromosome in normal females.

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.

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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


  1 in total

1.  Sequential sampling in clinical cytogenetics: a quality control viewpoint.

Authors:  M A De Arce; S P McManus
Journal:  J Med Genet       Date:  1988-09       Impact factor: 6.318

  1 in total

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