Intellectual disability/developmental delay (ID/DD) is a significant problem in child health affecting 2 to 3% of the population worldwide. While the underlying aetiology of ID/DD in a large proportion (about 50%) of these patients is unknown, 15 to 20% of the internationally reported cases detected using microarray technologies are due to copy number variants (CNVs), whereas only 3 to 5% of ID/DD can be identified with conventional cytogenetics. The Affymetrix® Cytoscan™ High Density (HD) Array (Affymetrix, Santa Clara, CA) containing over 2.4 million markers for copy number (CN) was used to detect genome-wide high resolution CN and single nucleotide polymorphisms (SNPs) in a cohort of 27 carefully selected patient samples. The patient sel...
Whilst the majority of inherited diseases have been found to be caused by single base substitutions,...
Array comparative genomic hybridization (array CGH) is now widely adopted as a first-tier clinical ...
International audienceBackground: Chromosomal microarray analysis (CMA) is currently the most widely...
PubMed ID: 25059023New array technologies have facilitated the analysis of submicroscopic chromosoma...
Purpose: Copy number variants have emerged as a major cause of human disease such as autism and inte...
Microarray genome analysis is realising its promise for improving detection of genetic abnormalities...
Chromosomal Microarray Analysis (CMA) is currently considered to be the first-tier clinical test for...
Genomic microarray analysis is rapidly replacing conventional chromosome analysis by molecular karyo...
Trabalho final de mestrado integrado em Medicina, área de Pediatria, apresentado á Faculdade de Medi...
Background: Array-comparative genomic hybridization (array-CGH) is a widely used technique to detect...
Background: Genomic deletions and duplications are important in the pathogenesis of...
Contains fulltext : 80578.pdf (publisher's version ) (Closed access)Microarray-bas...
Copy number variations (CNVs) in the human genome are inherent in both evolutionary progression as w...
Genomic microarrays have been implemented in the diagnosis of patients with unexplained mental retar...
Constitutional chromosomal imbalance has been recognized, for a long time, as an important cause of ...
Whilst the majority of inherited diseases have been found to be caused by single base substitutions,...
Array comparative genomic hybridization (array CGH) is now widely adopted as a first-tier clinical ...
International audienceBackground: Chromosomal microarray analysis (CMA) is currently the most widely...
PubMed ID: 25059023New array technologies have facilitated the analysis of submicroscopic chromosoma...
Purpose: Copy number variants have emerged as a major cause of human disease such as autism and inte...
Microarray genome analysis is realising its promise for improving detection of genetic abnormalities...
Chromosomal Microarray Analysis (CMA) is currently considered to be the first-tier clinical test for...
Genomic microarray analysis is rapidly replacing conventional chromosome analysis by molecular karyo...
Trabalho final de mestrado integrado em Medicina, área de Pediatria, apresentado á Faculdade de Medi...
Background: Array-comparative genomic hybridization (array-CGH) is a widely used technique to detect...
Background: Genomic deletions and duplications are important in the pathogenesis of...
Contains fulltext : 80578.pdf (publisher's version ) (Closed access)Microarray-bas...
Copy number variations (CNVs) in the human genome are inherent in both evolutionary progression as w...
Genomic microarrays have been implemented in the diagnosis of patients with unexplained mental retar...
Constitutional chromosomal imbalance has been recognized, for a long time, as an important cause of ...
Whilst the majority of inherited diseases have been found to be caused by single base substitutions,...
Array comparative genomic hybridization (array CGH) is now widely adopted as a first-tier clinical ...
International audienceBackground: Chromosomal microarray analysis (CMA) is currently the most widely...