Peroxisome Biogenesis Disorder, Complementation Group H

Known as: CGH 
 
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Single embryo transfer (SET) remains underutilized as a strategy to reduce multiple gestation risk in IVF, and its overall lower… (More)
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Highly Cited
2007
Highly Cited
2007
MOTIVATION Array CGH technologies enable the simultaneous measurement of DNA copy number for thousands of sites on a genome. We… (More)
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Highly Cited
2007
Highly Cited
2007
UNLABELLED CGHcall achieves high calling accuracy for array CGH data by effective use of breakpoint information from segmentation… (More)
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Highly Cited
2007
Highly Cited
2007
Autism and mental retardation (MR) are often associated, suggesting that these conditions are etiologically related. Recently… (More)
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Highly Cited
2005
Highly Cited
2005
Mental retardation (MR) occurs in 2%-3% of the general population. Conventional karyotyping has a resolution of 5-10 million… (More)
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Highly Cited
2005
Highly Cited
2005
Array CGH is a powerful technique for genomic studies of cancer. It enables one to carry out genome-wide screening for regions of… (More)
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Highly Cited
2004
Highly Cited
2004
MOTIVATION Genomic DNA regions are frequently lost or gained during tumor progression. Array Comparative Genomic Hybridization… (More)
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Highly Cited
2004
Highly Cited
2004
The underlying causes of learning disability and dysmorphic features in many patients remain unidentified despite extensive… (More)
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Highly Cited
2004
Highly Cited
2004
The development of solid tumors is associated with acquisition of complex genetic alterations, indicating that failures in the… (More)
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Highly Cited
2004
Highly Cited
2004
Microarray-CGH experiments are used to detect and map chromosomal imbalances, by hybridizing targets of genomic DNA from a test… (More)
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