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FRAXD gene

Known as: FRAXD, fragile site, aphidicolin type, common, fra(X)(q27.2) D 
National Institutes of Health

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Related topics

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FRA10A gene

Papers overview

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1992
1992
Experience with direct molecular diagnosis of fragile X.
The utility of the pfxa3 probe for direct molecular diagnosis of the fragile X (FRAXA) has been established. This probe detects… 
1992
1992
Frequency of the common fragile site at Xq27.2 under conditions of thymidylate stress: implications for cytogenetic diagnosis of the fragile-X syndrome.
The distal long arm of the X chromosome contains at least 2 fragile sites, the well known rare site at Xq27.3 (FRAXA), associated… 
1992
1992
Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome.
Cell cultures from 760 whole blood, amniotic fluid, chorionic villus sample, and peripheral umbilical blood sample specimens were… 
1990
1990
Location of FRAXD in Xq27.2. Fragile sites on the X chromosome.
1988
1988
A common fragile site at Xq27: theoretical and practical implications.
The fragile site at Xq27 (FRAXA) is associated with a common form of X-linked mental retardation (Martin-Bell syndrome). It is… 
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