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Get the free Cytogenomic SNP Microarray, FetalTest Fact Sheet

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Clinical Questionnaire for Reveal SNP Microarray Prenatal & POC LCA Use Only. Please place accessioning sticker here. This form should be completed when Reveal SNP Microarray Prenatal or POC is ordered.
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How to fill out cytogenomic snp microarray fetaltest

01
Ensure you have the appropriate consent and authorization for testing.
02
Collect a sample of the fetal DNA from the amniotic fluid or placental tissue.
03
Submit the sample to a laboratory that specializes in cytogenomic SNP microarray analysis.
04
The laboratory will process the sample and analyze the DNA for any chromosomal abnormalities or genetic variations.
05
Review the results with a genetic counselor or healthcare provider to discuss any findings and implications.

Who needs cytogenomic snp microarray fetaltest?

01
Cytogenomic SNP microarray fetal testing is typically recommended for pregnant women who are at increased risk for chromosomal abnormalities in the fetus.
02
This includes women who have had abnormal ultrasound findings, a family history of genetic disorders, advanced maternal age, or a previous pregnancy with a chromosomal abnormality.
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Cytogenomic SNP microarray fetaltest is a test that analyzes the genome of a fetus to identify any chromosomal abnormalities.
Cytogenomic SNP microarray fetaltest is usually recommended for pregnant women who are at high risk of having a baby with genetic disorders.
Cytogenomic SNP microarray fetaltest is typically performed by collecting a sample of the fetus's DNA, usually through a blood test or amniocentesis.
The purpose of cytogenomic SNP microarray fetaltest is to detect any genetic abnormalities in the fetus that could impact its health or development.
The cytogenomic SNP microarray fetaltest report typically includes information on any chromosomal abnormalities found in the fetus's genome.
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