Xq27.3

A chromosome band present on Xq.
National Institutes of Health

Topic mentions per year

Topic mentions per year

1985-2017
0102019852017

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Highly Cited
2010
Highly Cited
2010
BACKGROUND With the advent of second-generation sequencing, the expression of gene transcripts can be digitally measured with… (More)
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Highly Cited
1998
Highly Cited
1998
Fragile X syndrome is the most frequent cause of heritable mental retardation. Most patients have a mutation in the 5… (More)
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Highly Cited
1995
Highly Cited
1995
Fragile X mental retardation syndrome, the most common cause of hereditary mental retardation, is directly associated with the… (More)
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Highly Cited
1993
Highly Cited
1993
The vast majority of patients with fragile X syndrome show a folate–sensitive fragile site at Xq27.3 (FRAXA) at the cytogenetic… (More)
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Highly Cited
1991
Highly Cited
1991
Fragile X syndrome is the most frequent form of inherited mental retardation and is associated with a fragile site at Xq27.3. We… (More)
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Highly Cited
1991
Highly Cited
1991
Fragile X [fraX] syndrome is a common hereditary disorder associated with a fragile site marker at Xq27.3 which clinically… (More)
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Highly Cited
1991
Highly Cited
1991
BACKGROUND The fragile X syndrome, the most common form of inherited mental retardation, is caused by mutations that increase the… (More)
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1991
1991
We have used recombinant clones derived from microdissection of the fragile X region to characterize breakpoints around the… (More)
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1987
1987
We report the identification of a new RFLP detected by the DNA probe MN12, which is linked to both the fragile site on the X… (More)
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1985
1985
We have tested linkage between the locus for the fragile-X [fra(X)] syndrome at Xq27.3 and five polymorphic restriction sites… (More)
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