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Array-Based Comparative Genomic Hybridization

Known as: Array Based Comparative Genomic Hybridization, Array Comparative Genomic Hybridization 
 
National Institutes of Health

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Highly Cited
2015
Highly Cited
2015
Purpose: Although novel agents targeting the androgen–androgen receptor (AR) axis have altered the treatment paradigm of… Expand
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Review
2009
Review
2009
Copy number variation (CNV) is a source of genetic diversity in humans. Numerous CNVs are being identified with various genome… Expand
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Highly Cited
2009
Highly Cited
2009
Background Deregulation of EGFR signaling is common in non-small cell lung cancers (NSCLC) and this finding led to the… Expand
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Highly Cited
2009
Highly Cited
2009
To evaluate the use of array comparative genomic hybridization (aCGH) for prenatal diagnosis, including assessment of variants of… Expand
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Highly Cited
2008
Highly Cited
2008
Autism is a childhood neurodevelopmental disorder with a strong genetic component, yet the identification of autism… Expand
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Highly Cited
2008
Highly Cited
2008
BACKGROUND One genetic mechanism known to be associated with autism spectrum disorders (ASD) is chromosomal abnormalities. The… Expand
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Highly Cited
2008
Highly Cited
2008
BackgroundDNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative… Expand
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Review
2008
Review
2008
Array comparative genomic hybridization (aCGH) is a technique enabling high-resolution, genome-wide screening of segmental… Expand
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Highly Cited
2007
Highly Cited
2007
Cervical cancer (CC) cells exhibit complex karyotypic alterations, which is consistent with deregulation of numerous critical… Expand
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Highly Cited
2006
Highly Cited
2006
To identify genetic events underlying the genesis and progression of multiple myeloma (MM), we conducted a high-resolution… Expand
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