Xq27

A chromosome band present on Xq
National Institutes of Health

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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… (More)
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2005
2005
Genetic linkage studies indicate that germline variations in a gene or genes on chromosome Xq27-28 are implicated in prostate… (More)
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2003
2003
Linkage studies have implicated a prostate cancer susceptibility locus at Xq27-28 (termed HPCX), estimated to be responsible for… (More)
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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… (More)
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2001
2001
OBJECTIVES A recent linkage analysis of 360 families at high risk for prostate cancer identified the q27-28 region on chromosome… (More)
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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… (More)
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1999
1999
Human Xq27 contains candidate regions for several disorders, yet is predicted to be a gene-poor cytogenetic band. We have… (More)
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1997
1997
Clinical reexamination and DNA linkage analysis were carried out in an X-linked progressive cone dystrophy (XLPCD) family… (More)
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1987
1987
Sister chromatid exchange (SCE) was evaluated in peripheral blood lymphocytes cultured from normal subjects, fragile X carrier… (More)
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Highly Cited
1979
Highly Cited
1979
The expression of heritable fragile sites on human chromosomes has been shown to be dependent upon composition of the tissue… (More)
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