Answer:
According to Punnett Square, what can be concluded from Huntington's disease is that the disease is autosomal dominant.
Explanation:
Huntington's disease is characterized as a neurodegenerative condition, which affects body movements and progressively decreases some higher brain functions.
Inheritance plays a determining role in Huntinton's disease, being a disease transmitted from parents to children with an autosomal dominant pattern, that is, all <u>individuals with the defective gene (H) will have the disease</u>, while the <u>absence of the gene (rr) also guarantees the absence of this condition</u>.
The other options are not correct because:
- <em>Inheritance of Huntington's disease is not sex-linked.
</em>
- <em>The allele that determines the Hungtinton's disease is not recessive.</em>
Hey there,
Question: <span>Which scientists are credited for the events described in the development of the cell theory?
Answer: The cell was discovered by Robert Hooke. But the first cell's theory was discovered by T</span>heodor Schwann<span> and </span><span>Matthias Jakob Schleiden.
Question: </span><span>Who observed a living cell in a pond?
Answer: </span><span>Anton Von Leeuwenhoek
Question: </span><span>Used the word cell for the structures he observed?
Answer: Robert Hooke
Hope this helps: D
<em>~Top♥</em>
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Explanation: XX because she is female. Since she is not color blind one of the pair has to be XC. Since she is a carrier of color blindness she has to have the recessive gene as well, so the other has to be Xc.
Answer:
one that recognizes a 2 base pair sequence would cut DDNA every 16 bases. A 3 base pair recognition site would be found every 64 bases.
