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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A wall located outside the cell membrane provides the cell support, and protection against mechanical stress or damage from osmotic rupture and lysis. The major component of the bacterial cell wall is peptidoglycan or murein. This rigid structure of peptidoglycan, specific only to prokaryotes, gives the cell shape and surrounds the cytoplasmic membrane.
Modern H. sapiens differ from the archaic form in that moderns have a high, vertical forehead, a mental eminene; and lack occipital bun. Modern homo sapiens have distinguishing features such as they have a short base, a high braincase, back of the skull is rounded and indicates a reduction in the neck muscles, face is reasonably small with a projecting nose bone among other features that makes them different from the other sapiens.
Answer: Proteins and Carbohydrates
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