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 …

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 various types of …

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, that we call “deletions” or “duplications.” These …

Aug 5, 2025 · Chromosomal microarray analysis (CMA) is a high-resolution genetic test. It detects very small missing or extra pieces of chromosomes, known as deletions or duplications.

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 comparative …

Chromosomal Microarray Analysis (CMA) is a high-resolution genetic diagnostic tool used to analyze an individual’s complete set of chromosomes. This technology detects subtle, genome …

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 other tissue sample (in …

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 …

Miller DT, et al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

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 developmental …