Genetic screening
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Genetic screening report of a committee of the Health Council of the Netherlands. by Gezondheidsraad (Netherlands)

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Published by Gezondheidsraad in [Rijswijk] .
Written in English

Subjects:

  • Genetic disorders -- Diagnosis.,
  • Human chromosome abnormalities -- Diagnosis.,
  • Medical screening.

Book details:

Classifications
LC ClassificationsRB155.6 .G483 1994
The Physical Object
Pagination149 p.
Number of Pages149
ID Numbers
Open LibraryOL17408722M

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Genetic testing looks for specific inherited changes (variants) in a person’s genes. Genetic variants can have harmful, beneficial, neutral (no effect), or unknown or uncertain effects on the risk of developing diseases. Harmful variants in some genes are known to be associated with an increased risk of developing cancer. These inherited. NOTICE: Our Sonic Healthcare pathology laboratories are providing urgent testing supporting the government’s response to the COVID pandemic. This additional activity could cause some delays in the reporting of non-urgent genetic tests but as of yet this is not the case. There will be no change to the usual reporting times for time-critical genetic tests such as non-invasive . Doctors, scientists, genetic counselors, and computer experts are all on the team (like a group of people sitting down to read and talk about a book). To decide which variant causes the disease you are interested in, the team looks at your results (your list of variants), your symptoms, and your family history. Prenatal genetic testing is used to detect abnormalities in the genes or chromosomes of a fetus before birth. Current guidelines recommend that all pregnant women be offered maternal serum screening tests to identify pregnancies that are at increased risk for a trisomy disorder (such as Down syndrome).