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Xq27

A chromosome band present on Xq
National Institutes of Health

Papers overview

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Highly Cited
2006
Highly Cited
2006
A family history of disease is a strong risk factor for testicular germ cell tumour (TGCT). In order to identify the location of… Expand
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Highly Cited
2004
Highly Cited
2004
SummaryThere were 18 individuals found to have a constitutional chromosome fragility causing an increase in break frequency. For… Expand
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Highly Cited
2004
Highly Cited
2004
Background: Osteoporosis is a major public health problem, mainly quantified by low bone mineral density (BMD). The majority of… Expand
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Highly Cited
2001
Highly Cited
2001
Background: Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the X-linked methyl CpG binding protein 2… Expand
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Highly Cited
2000
Highly Cited
2000
Testicular germ-cell tumours (TGCT) affect 1 in 500 men and are the most common cancer in males aged 15–40 in Western European… Expand
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Highly Cited
1993
Highly Cited
1993
FRAXA is unique amongst fragile sites in that it is intimately involved with a specific clinical phenotype, the fragile X… Expand
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1991
1991
The development of the human gene map in the region of the fragile X mutation (FRAXA) at Xq27 has been hampered by a lack of… Expand
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Highly Cited
1987
Highly Cited
1987
A mechanism is proposed for the inheritance and expression of the fragile-X-linked syndrome of mental retardation in humans. Two… Expand
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Highly Cited
1980
Highly Cited
1980
Twenty-three families with X-linked mental retardation were examined for the presence of a fragil site on the long arm of the X… Expand
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Highly Cited
1979
Highly Cited
1979
  • G. Sutherland
  • American journal of human genetics
  • 1979
  • Corpus ID: 10749104
The expression of heritable fragile sites on human chromosomes has been shown to be dependent upon composition of the tissue… Expand
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