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.

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

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 expression levels …

Understanding and diagnosing the potential causes of genetic conditions is an essential first step in optimizing an effective treatment plan. CMA is recommended for individuals thought to have a …

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 autism spectrum …

Follow-up testing for individuals with unexplained developmental delay or intellectual disability, autism spectrum disorders, or congenital anomalies with a previously normal conventional chromosome study.

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 “duplications.” In this …

Chromosomal Microarray Analysis provides comprehensive genetic testing for the most common chromosomal conditions as well as a large number of severe genetic conditions not detected by …

Chromosomal microarray (CMA) is increasingly utilized for genetic testing of individuals with unexplained developmental delay/intellectual disability (DD/ID), autism spectrum disorders (ASD), or …