Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan.
|
30581099 |
2019 |
Developmental delay (disorder)
|
0.100 |
GeneticVariation
|
phenotype |
BEFREE |
Using array CGH, 262 patients with deletions and 215 with duplications were identified and tested for their association with four phenotypes (developmental delay, dysmorphic features, autism group of disorders, and epilepsy/seizures).
|
30542208 |
2019 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
We identified a deleted region of 496 kb by whole genome array CGH in a patient who fulfilled criteria for 2q37 microdeletion syndrome with developmental delay, microcephaly, hypoplasia of the corpus callosum, hand wringing, toe walking, and seizures.
|
26238961 |
2015 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
A cohort of patients (n = 1590) referred for array-CGH testing of undiagnosed learning disability and developmental delay by a single NHS regional clinical genetics service (South East Thames Regional Genetics Service), were split into a before-and-after design where 742 patients had array-CGH as a second-line test (before group-comparator intervention) and 848 patients had array-CGH as a first-line test (after group-evaluated intervention).
|
25894741 |
2015 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Our results further support the notion that copy-number variants significantly contribute to the genetic etiology of DD/ID and emphasize the efficacy of the detection of novel candidate genes for neurodevelopmental disorders by whole-genome array CGH.
|
24297458 |
2014 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies.
|
25016475 |
2014 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Array CGH is a useful diagnostic tool in clinical settings in patients with developmental delay or intellectual disability combined with facial abnormalities or failure to thrive.
|
24142652 |
2013 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders.
|
22872102 |
2013 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
A parallel study of different array-CGH platforms in a set of Spanish patients with developmental delay and intellectual disability.
|
23524024 |
2013 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
|
22283495 |
2013 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
In this study, oligonucleotide-based array-CGH was used to investigate a panel of 23 patients with mental retardation and developmental delay, dysmorphic features or congenital anomalies.
|
22123463 |
2011 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Based on our experiences, array-CGH is recommended as the first-step analysis in the genetic evaluation of patients with DD and/or MCA.
|
20486943 |
2011 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Here, we describe a collaborative study reporting a new cohort of 12 index patients and 13 relatives carrying a heterozygous BP4-BP5 microdeletion out of a series of 4625 patients screened by array-CGH for DD.
|
20236110 |
2010 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Deletion (1)(p32.2-p32.3) detected by array-CGH in a patient with developmental delay/mental retardation, dysmorphic features and low cholesterol: A new microdeletion syndrome?
|
18680192 |
2008 |
Developmental delay (disorder)
|
0.100 |
GeneticVariation
|
phenotype |
BEFREE |
Using microarray CGH (aCGH) and gene expression arrays we studied a child with t(15;22)(q26.1;q11.2), developmental delay and mild dysmorphic features.
|
18203177 |
2008 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Characterization by array-CGH of an interstitial de novo tandem 6p21.2p22.1 duplication in a boy with epilepsy and developmental delay.
|
18463015 |
2008 |
Developmental delay (disorder)
|
0.100 |
GeneticVariation
|
phenotype |
BEFREE |
Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features.
|
17568414 |
2007 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
The study however further strengthens the fact that genome-wide analysis by array CGH in individuals with developmental delay and mental retardation is very useful in detecting such hidden interstitial chromosomal rearrangements.
|
17268193 |
2007 |
Developmental delay (disorder)
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
Array-CGH has become an important tool for the detection of chromosome aberrations and has the potential to identify genes involved in developmental delay and dysmorphism.
|
16141005 |
2005 |