Array-Based Comparative Genome Hybridization in Clinical Genetics
- 1 September 2006
- journal article
- case report
- Published by Springer Nature in Pediatric Research
- Vol. 60 (3) , 353-358
- https://doi.org/10.1203/01.pdr.0000233012.00447.68
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH)Journal of Medical Genetics, 2005
- X chromosome array-CGH for the identification of novel X-linked mental retardation genesEuropean Journal of Medical Genetics, 2005
- Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresJournal of Medical Genetics, 2004
- Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal AbnormalitiesAmerican Journal of Human Genetics, 2003
- Does chromosome 22 have anything to do with sex determination: Further studies on a 46,XX,22q11.2 del maleAmerican Journal of Medical Genetics Part A, 2003
- Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletionsHuman Molecular Genetics, 2003
- Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detectionJournal of Molecular Medicine, 2003
- A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsHuman Molecular Genetics, 2002
- High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarraysNature Genetics, 1998
- Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalancesGenes, Chromosomes and Cancer, 1997