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:
DNA replication
Explanation:
Synthesis is the stage characterized by DNA replication. It is after the G1 phase
2 4 and 6 i took the course and that's right
Answer:
The mRNA molecule will be synthesized running in the 5' to 3' direction.
Explanation:
From the DNA sequence:
5'-ATCGTACCGTTA-3'
3'-TAGCATGGCAAT-5'
mRNA sequence is
5'-AUCGUACCGUUA-3'
Amino acid sequence will thus be:
Ileu-val-pro-leu.
