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Q: Which technique is used to collect fetal cells during pregnancy for genetic testing?
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What techniques is used to collect fetal cells during pregnancy for genetic testing?

amniocentesis


Which of the testing technique immediately follows the unit testing?

module testing


Which of the testing technique immediatle follow the unit testing?

sub system testing


What genetic material can be extracted from your body tissues and used to create a profile to identify a victim or suspect?

Any cell from your body, which have the nucleus, will do for genetic material. So you can collect the blood, which have white blood cells, will do. Biopsy from any part gives you enough cells for the genetic material, you need for genetic testing.


What is saliva sample testing?

Saliva sample testing is a technique used to collect samples of a person's saliva, or spit, to check for or monitor certain drugs, hormones (chemical messengers from one cell or group of cells to another), antibodies


How are patients prepared for genetic testing?

Most tests for genetic diseases of children and adults are done on blood. To collect the 5-10 mL of blood needed, a healthcare worker draws blood from a vein in the inner elbow region.


Where can one find more information about paternity testing?

There are many online websites to find out more information about paternity tests. Some of these websites include the American Pregnancy Association, DNA Genetic Connections, and DNA Testing.


How is genetic testing for breast cancer done?

Genetic testing for the breast cancer genes is doing via blood testing. Previous counseling is a normal requirement.


How many people use genetic testing?

30% of people or doctors use genetic testing because of the change in chromosomes


Is there genetic testing for retinoblastoma?

Yes, there is, and it is recommended if you have a family history of retinoblastoma. One lab that performs genetic testing is Retinoblastoma Solutions,


What is the role of genetic testing in spinocerebellar ataxia?

Genetic testing of at-risk family members can be performed when an affected individual has a known genetic mutation. Testing of high-risk family members without symptoms raises many issues.


How can a person be screened for a genetic disorder such as Huntingtons disease?

By genetic testing. This involves laboratory testing on a small blood sample. It will normally be accompanied by family history tracking, and a physical examination, along with counseling.