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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Only one parent, and the same chromosome
<span>number as the parent.</span>
The main difference between haploid cells and diploid cells is diploid cells have two complete sets of chromosomes, while haploid cells only have one complete set of chromosomes.
H. The suns energy is conducted to your skin by the glass.