Significados de genomic hybridization en inglés

In this report, we apply array-based comparative genomic hybridization on 11 LPL samples.

Comparative genomic hybridization evaluation of the sample revealed a normal profile.

Chromosomal imbalances were detected from average comparative genomic hybridization profiles for each entity.

Results: No segregating rare copy number variants were detected by array comparative genomic hybridization.

Purpose: Array comparative genomic hybridization is available for the evaluation of autism spectrum disorders.

The patient's oligonucleotide array-comparative genomic hybridization profile revealed no abnormality.

A recent comparative genomic hybridization analysis revealed frequent losses of chromosome 4 in breast carcinomas.

One patient had had an abnormal karyotype; none had prior array comparative genomic hybridization testing.

We describe 2 reports of array comparative genomic hybridization analysis of de novo congenital melanoma.

Twenty-five primary carcinomas were analyzed by comparative genomic hybridization.

The yield of array comparative genomic hybridization in the adult autism spectrum disorder population is unknown.

Microarray-based comparative genomic hybridization analysis of S. Derby and S. Enteritidis revealed more than 350 genetic differences.

With microarray competitive genomic hybridization, genomewide chromosomal copy number changes can be studied with high resolution and sensitivity.

Experimental design: Using array comparative genomic hybridization, we evaluated the copy number aberrations of genes regulating thymus development.

Array comparative genomic hybridization detects segmental DNA copy number alterations in tumor DNA relative to a normal control.

The remaining two variants were identified by array-comparative genomic hybridization and consisted of a partial deletion of FBXO11.