Answer:
Heart valve problems
Explanation:
Marfan syndrome is a syndrome caused by a genetic defect in a gene that is important to define the structure of a protein called fibrin 1 which makes a part of connective tissue.
One of the main problems with people having this disorder is heart problems. Most of the people with Marfan syndrome have damaged aorta. Aorta plays an important role in carrying blood from the heart to other body parts. Therefore heart valve problem is the clinical finding that would be a treatment priority for this client.
Other symptoms associated with these disorders are tall aperture, long and disproportionate arm and leg, abnormal spine structure, etc.
It explodes
hope this helps lol
If one wishes to clone a gene using typical restriction endonucleases, how does the restriction endonuclease identify the appropriate cut sites in the genome using the palindromic sequence.
Restriction endonucleases are a family of enzymes usually found in bacteria that cuts DNA at a specific sequence called recognition site. There are three type of restriction endonuclease Type I, Type II, and Type III.
Each endonuclease recognizes a particular sequence called palindromic sequence which is a sequence that reads the same sequence in both the strands either reading from the 3 prime end or 5 prime end.
The endonuclease cuts the palindromic sequence in such a way that it produces sticky ends.
To learn more about restriction endonucleases here
brainly.com/question/14755040
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The first is reflection of moonlight
