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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
BackgroundSingle embryo transfer (SET) remains underutilized as a strategy to reduce multiple gestation risk in IVF, and its… Expand
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Highly Cited
2009
Highly Cited
2009
The description of optical fields in terms of their eigenmodes is an intuitive approach for beam characterization. However, there… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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Highly Cited
2004
Highly Cited
2004
BackgroundMicroarray-CGH experiments are used to detect and map chromosomal imbalances, by hybridizing targets of genomic DNA… Expand
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Review
1999
Review
1999
Abstract In B-cell chronic lymphocytic leukemia (B-CLL) clonal chromosome aberrations are detected in approximately 40–50% of… Expand
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Highly Cited
1996
Highly Cited
1996
Comparative genomic hybridization was used to screen the DNA extracted from histologically defined tissue sections from… Expand
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