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3q26.1

A chromosome band present on 3q.
National Institutes of Health

Papers overview

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2013
2013
Even with significant advances in technology, few studies of structural variation have yet resolved to the level of the precise… Expand
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2013
2013
Colorectal cancers (CRCs) exhibit multiple genetic alterations, including allelic imbalances (copy number alterations, CNAs) at… Expand
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2013
2013
Despite the advances in diagnosis and treatment of oral squamous cell carcinoma (OSCC), mortality and morbidity rates have not… Expand
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2012
2012
Research suggests that clinical symptom dimensions may be more useful in delineating the genetics of bipolar disorder (BD) than… Expand
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Highly Cited
2011
Highly Cited
2011
Attention-deficit/hyperactivity disorder (ADHD) is a common, highly heritable neurodevelopmental syndrome characterized by… Expand
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2009
2009
The study of variation found in DNA is fundamental in human genetic studies. Single nucleotide polymorphisms (SNPs) are simple to… Expand
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2009
2009
Familial adenomatous polyposis (FAP) is an autosomal dominantly inherited form of colorectal cancer (CRC) caused by mutation in… Expand
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2004
2004
A total of 127 adult de novo acute myelocytic leukemia (AML) patients were analyzed by comparative genomic hybridization (CGH) at… Expand
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Highly Cited
2002
Highly Cited
2002
For a better understanding of genetic alterations in head and neck squamous cell carcinoma (HNSCC), we applied comparative… Expand
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Highly Cited
1998
Highly Cited
1998
We used comparative genomic hybridization (CGH) to screen for DNA copy number changes in 34 specimens from 27 cases of mantle… Expand
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