The Cytogenetics Laboratory performs chromosome analysis, fluorescence in situ hybridization (FISH) and single nucleotide polymorphism (SNP) microarray testing.

This test compares the patient’s sample to a normal control sample to find very small missing or extra chromosome pieces that cannot be seen under a microscope.

Aug 15, 2020 · A DNA microarray is a tool used to determine whether the DNA from a particular individual contains a mutation in genes.

A DNA microarray (also commonly known as a DNA chip or biochip) is a collection of microscopic DNA spots attached to a solid surface. Scientists use DNA microarrays to measure the …

Quest helps you harness the power of chromosomal microarray analysis (CMA) Understanding and diagnosing the potential causes of genetic conditions is an essential first step in optimizing …

A chromosomal microarray analysis, also called microarray or array, is a type of genetic test that looks for missing or extra portions of a chromosome. We call these “deletions” or …

A microarray is a laboratory technique used in the study and analysis of biological molecules, particularly DNA and proteins, in which a probe of interest is affixed in a grid pattern to the …

We provide an evidence-based summary of clinical cytogenetic testing comparing CMA to G-banded karyotyping with respect to technical advantages and limitations, diagnostic yield for …

This test will detect chromosomal imbalances that could be associated with developmental delay/congenital anomalies. It provides detection of possible uniparental disomy of any …

SNP microarray is recommended as a first-tier genetic test for the postnatal evaluation of individuals with multiple congenital anomalies, developmental delay, intellectual disability, and …