A study identifies motor delay and hypotonia as key predictors of genetic diagnoses, aiding clinicians in neurodevelopmental ...

Expert Rev Mol Diagn. 2013;13(6):601-611. In other situations, normal microarray analysis in the presence of an abnormal karyotype, such as marker chromosomes, is reassuring, as it indicates that ...

The sequencing of the human genome afforded the development of chromosomal microarrays that ... In addition, SNPs may be used in microarray construction that not only detect copy number variations ...

CNV and SV with phenotypic heterogeneity and incomplete penetrance were more likely to cause fetal isolated VSD than chromosomal aberration. Clinicians should be aware of the benefits and implications ...

Program for Cancer and Cell Biology, Department of Human Anatomy, Histology and Embryology, School of Basic Medical Sciences; Peking University International Cancer Institute; and State Key Laboratory ...

The Thermo Scientific KingFisher PlasmidPro Maxi Processor (PlasmidPro) has been introduced by Thermo Fisher Scientific Inc. as the only fully automated maxi-scale plasmid DNA (pDNA) purification ...

Approximately 2.4% to 24.4% of total cfDNA in maternal blood is placental (1 Trusted Source Noninvasive prenatal test for fetal chromosomal ... Traditional microarray- and targeted ...

A microarray is a set of samples, for example DNA, RNA or proteins, arranged on a solid substrate or chip, such as a glass slide or silicon film, that is used in high throughput experiments.

The use of genome wide single nucleotide polymorphism (SNP) arrays for high resolution molecular cytogenetic analysis using a combination of quantitative and genotype analysis is well established.