Explanation:
Option 1.
4y=12
Dividing 4 both sides
y=3
Division property should be used.
Option 2.
Cross multiplying each other,
y=12(4)
y=48
Option 3.
2(4y)=12
Opening bracktet in LHS
8y=12
Dividing both sides by 8 i.e.
Division property is used.
Option 4.
y+4=12
Subtracting both sides by 4 i.e.
Y+4-4=12-4
y=8
Subtraction property is used.
<em><u>It means that in option (4) Soo-Jung used the subtraction property of equality to solve an equation for y.</u></em>
Metal -a solid material that is hard, shiny, malleable, fusible, and ductile, with electrical and thermal conductivity.\
nonmetal an element or substance that is not a metal.
Answer:
Thymidine dimers is likely to be repair as soon as it is originated but if left unrepaired then it causes frame shift mutations.
Explanation:
In case of Bacterium if UV irradiation induces covalent linkage of two thymidine present adjacently to each other or on a single strand to make thymidine dimers.
These either excised via DNA repair enzyme like Endonuclease V and the proof reading activity of DNA polymerase I enzyme help in incorporation of nucleotide by taking the unmutated original strand as a template.
These dimers if not excised before second round of replication than the sequence of newly synthesized strand will be altered. As DNA polymerase III enzyme read thymidine dimers as single thymidine nucleotide and incorporate only 1 adenine in the newly synthesizing complementary strand which results in frame shift mutations
It is the mutation in which reading frame of codons is shifted or altered due to deletion or addition of a single nucleotide.
Answer:
CPT® Index - 96040
icd-10-cm code - Q99.2
Explanation:
Here in this case the diagnosis came out with fragility in X chromosome. This is some thing related with medical genetics. Hence, the CPT® Index for this scenario would be 96040. As per the American Medical Association, CPT® Index 96040 cover cases that fall into the category of “Medical Genetics and Genetic Counseling Services” which also involves counseling either with the patient or family for 30 minutes. The icd-10-cm code – Q99.2 deals with the problems associated with genetic abnormality
Hence, the answer is
CPT® Index - 96040
icd-10-cm code - Q99.2
Answer:
Deletion
Explanation:
ATGCCATG<u>G</u>CATTGA
-->
ATGCCATGCATTGA
Comparing the two sequences, you can see that one G nucleotide is missing in the new sequence compared to the original.
This is a single nucleotide deletion, where one nucleotide is lost from the sequence. Otherwise, the sequence is entirely unchanged.
