Amniocentesis is a freshly established test for identifying fetal duchenne's muscular dystrophy.
<h3>What is tested for during an amniocentesis?</h3>
Amniocentesis is a test that may be recommended to you during pregnancy to determine whether your unborn child has a chromosomal or genetic disorder like Down syndrome, Edwards syndrome, or Patau's syndrome.
<h3>What exactly does an amniocentesis entail?</h3>
A little sample of amniotic fluid is removed during an amniocentesis operation for testing. This is the fluid that a pregnant woman's fetus is enclosed in. The amniotic fluid shields the fetus from harm and is transparent and pale yellow in color. provides infection protection.
<h3>What takes place after a positive amniocentesis test?</h3>
If the test yields a positive result, the fetus may have the genetic disorder. To confirm this, more testing are sometimes required.
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<u>brainly.com/question/17392704</u>
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Answer:
A. Stores DNA
Explanation:
The nucleus of the cell holds the genetic information of a cell, which is known as DNA. The nucleus is also known as the control center of the cell because it dictates the type of proteins that will be made. These proteins are used for the cellular processes that determines its function.
Characteristic of many trans-membrane proteins is the presence of tyrosines and tryptophans at the aqueous interface .These amino acids serve as interfacial anchors that can interact simultaneously with the membrane hydrophobic interior and the aqueous exterior.
Yes
Enhancing safety
Reducing error
Enhancing comfort
Increasing productivity
Answer:
provide structure and support for cells. On a larger scale, they also allow the body to move. These proteins bind and carry atoms and small molecules within cells and throughout the body.
