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*FMU3264×PEDIATRIC POPULATION CHROMOSOMAL SNP MICROARRAY TEST Page 1 of 2 INFORMATION AND CONSENT FORM IS SINGLE NUCLEOTIDE POLYMORPHISM (SNP) CHROMOSOMAL MICROARRAY (CMA) PERFORMED? Each segment

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How to fill out chromosomal microarray is a

01

Obtain a sample of DNA from the individual being tested

02

Amplify the DNA to increase the amount available for analysis

03

Label the DNA with different colors to distinguish between the individual's chromosomes

04

Hybridize the labeled DNA to a chip or slide containing known genetic sequences

05

Use a scanner to detect the amount of labeled DNA bound to each genetic sequence

06

Analyze the data to identify any deletions, duplications, or other chromosomal abnormalities

Who needs chromosomal microarray is a?

01

Individuals with unexplained developmental delays or intellectual disabilities

02

Individuals with multiple congenital anomalies

03

Individuals with autism spectrum disorder

04

Individuals with a family history of chromosomal abnormalities

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What is chromosomal microarray is a?

Chromosomal microarray is a genetic test that detects tiny missing or extra pieces of chromosomes.

Who is required to file chromosomal microarray is a?

Medical professionals who suspect a genetic disorder may recommend chromosomal microarray testing for their patients.

How to fill out chromosomal microarray is a?

Chromosomal microarray testing requires a blood sample or other tissue sample from the patient, which is then analyzed for any chromosomal abnormalities.

What is the purpose of chromosomal microarray is a?

The purpose of chromosomal microarray is to identify genetic disorders, developmental delays, and other medical conditions caused by chromosomal abnormalities.

What information must be reported on chromosomal microarray is a?

The testing report must include details of any genetic abnormalities found, as well as recommendations for further evaluation or treatment.

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