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Peroxisome Biogenesis Disorder, Complementation Group H

Known as: CGH 
National Institutes of Health

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Broader (1)

Peroxisomal Disorders

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2013
Highly Cited
2013
Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing
In clinical diagnostics, both array comparative genomic hybridization (array CGH) and single nucleotide polymorphism (SNP… 
Highly Cited
2009
Highly Cited
2009
Complete modal decomposition for optical fibers using CGH-based correlation filters.
The description of optical fields in terms of their eigenmodes is an intuitive approach for beam characterization. However, there… 
Highly Cited
2009
Highly Cited
2009
SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis
Objective:  We aimed to determine the type, frequency, and size of microchromosomal copy number variations (CNVs) affecting the… 
Review
2008
Review
2008
CGHcall: Calling aberrations for array CGH tumor profiles.
1 Overview CGHcall allows users to make an objective and e ective classi cation of their aCGH data into copy number states (loss… 
Highly Cited
2008
Highly Cited
2008
Mathematical modeling of triangle-mesh-modeled three-dimensional surface objects for digital holography.
We develop a mathematical model of triangle-mesh-modeled three-dimensional (3D) surface objects for digital holography. The… 
Highly Cited
2007
Highly Cited
2007
Resolving the resolution of array CGH.
Highly Cited
2006
Highly Cited
2006
Single-cell chromosomal imbalances detection by array CGH
Genomic imbalances are a major cause of constitutional and acquired disorders. Therefore, aneuploidy screening has become the… 
Highly Cited
2005
Highly Cited
2005
Genome‐wide array‐based comparative genomic hybridization of natural killer cell lymphoma/leukemia: Different genomic alteration patterns of aggressive NK‐cell leukemia and extranodal Nk/T‐cell…
Natural killer (NK) cell lymphomas/leukemias are highly aggressive lymphoid malignancies, but little is known about their genomic… 
Highly Cited
2002
Highly Cited
2002
Genomic gains and losses are similar in genetic and histologic subsets of rhabdomyosarcoma, whereas amplification predominates in embryonal with anaplasia and alveolar subtypes
In this investigation, we selected PAX3/FKHR and PAX7/FKHR fusion transcript–positive and –negative alveolar rhabdomyosarcomas… 
Highly Cited
1972
Highly Cited
1972
Using computer generated holograms to test aspheric wavefronts.
The use of computer generated holograms for the testing of aspheric wavefronts is described. An analysis of the errors produced… 
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