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

Your health care provider has ordered a genetic test called a microarray (MY-cro-a-ray) analysis. The test is also known as chromosomal microarray, whole genome microarray, array …

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 …

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

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 …

Based on current published guidelines, exome or genome sequencing can now be considered as first-tier tests for patients with unexplained epilepsy, developmental delay, intellectual …

IN SUMMARY Chromosome microarray (CMA) testing is a detailed genetic test that can look for extra or missing pieces of genetic material or DNA The test can be done on a blood, saliva or …

Aug 15, 2020 · Researchers have already discovered over 800 different mutations in BRCA1 alone.The DNA microarray is a tool used to determine whether the DNA from a particular …

A chromosome microarray (CMA; also known as a chromosomal microarray or molecular karyotype) is a powerful diagnostic tool that is used to identify genetic causes of illness and …

Chromosomal microarray (CMA) is a high-resolution method for detecting copy number changes (gains or losses) across the entire genome in a single assay and is sometimes called a …