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Frequency of fragile X chromosome in normal females
Author(s) -
Abuelo Dunne,
Castree Katherine,
Pueschel Siegfried,
PadreMendoza Teresita,
Zolnierz Kathy
Publication year - 1985
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1985.tb00366.x
Subject(s) - chromosomal fragile site , fragile x syndrome , x chromosome , fragile x , biology , genetics , chromosome , gene
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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