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15q26.1

A chromosome band present on 15q
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
In a three-stage genome-wide association study among East Asian women including 22,780 cases and 24,181 controls, we identified 3… Expand
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Highly Cited
2005
Highly Cited
2005
Congenital diaphragmatic hernia (CDH), a life-threatening anomaly, is a major cause of pediatric mortality. Although the disease… Expand
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Highly Cited
2005
Highly Cited
2005
Congenital diaphragmatic hernia (CDH) has an incidence of 1 in 3,000 births and a high mortality rate (33%-58%). Multifactorial… Expand
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Highly Cited
2004
Highly Cited
2004
ARC syndrome (OMIM 208085) is an autosomal recessive multisystem disorder characterized by neurogenic arthrogryposis multiplex… Expand
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Highly Cited
2004
Highly Cited
2004
Spondylocostal dysostosis (SCD) is a term given to a heterogeneous group of disorders characterized by abnormal vertebral… Expand
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Highly Cited
2001
Highly Cited
2001
Editor—Reports of patients with terminal de novo deletions of chromosome 15q26 are rare. Excluding cases of ring chromosome 15… Expand
Highly Cited
1999
Highly Cited
1999
BACKGROUND Elevated blood pressure is a risk factor for cardiovascular, cerebrovascular, and renal diseases. Complex mechanisms… Expand
Review
1996
Review
1996
Mutation of the Bloom's syndrome (BS) gene, BLM, results in genomic instability. As the first step toward positional cloning of… Expand
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Highly Cited
1994
Highly Cited
1994
By the principle of identity by descent, parental consanguinity in individuals with rare recessively transmitted disorders… Expand
Highly Cited
1991
Highly Cited
1991
We report on an infant with a previously undescribed chromosome 15 deletion (q26.1----qter) and compare the clinical findings… Expand