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Get the free Prenatal genetic carrier testing using triple disease screening

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PRENATAL TESTING REQUISITIONSPECIMENS: 1428 Madison Ave., Rm AB225, New York, NY 10029 MAIL: One Gustav L. Levy Place, Box 1497, New York, NY 100296574 Phone: 8002986470 / Fax: 2122410139 Tax ID#
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How to fill out prenatal genetic carrier testing

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How to fill out prenatal genetic carrier testing

01
Schedule an appointment with a healthcare provider who specializes in prenatal genetic testing
02
Discuss the benefits and risks of the test with your provider
03
Provide a blood sample for testing
04
Wait for the results and follow up with your provider for further guidance

Who needs prenatal genetic carrier testing?

01
Individuals with a family history of genetic disorders
02
Couples who are planning to have children and want to assess their risk of passing on genetic conditions
03
Women who are over the age of 35 or have had previous pregnancies with genetic abnormalities
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Prenatal genetic carrier testing is a screening test that can identify genetic mutations that may be passed on to a child.
Pregnant individuals or couples planning to have children may choose to undergo prenatal genetic carrier testing.
Prenatal genetic carrier testing is typically done through a blood or saliva sample, which is then sent to a laboratory for analysis.
The purpose of prenatal genetic carrier testing is to assess the risk of a child inheriting certain genetic disorders.
The test results indicating whether the individual carries any specific genetic mutations that could be passed on to the child.
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