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VARVARA [1.3K]
4 years ago
7

What is the probability that a human sperm cell will carry an X chromosome ?

Biology
1 answer:
LUCKY_DIMON [66]4 years ago
4 0

50% probability that a human sperm cell will carry an X chromosome

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LET'S CHECK
Daniel [21]

Answer:

I.

4) The deoxygenated blood then travels through the veins and enters the right side of the heart.

1) The blood leaves the heart through the aorta.

2) The blood travels throughout the body via the arteries to the capillaries.

3) In the capillaries, the exchange of nutrients and gases occurs. Oxygen is absorbed by the cells while carbon dioxide is released into the blood.

II.

2) Exchange of gases happens as oxygen is received by the blood and carbon dioxide is released.

1) The deoxygenated blood flows from the right side of the heart to go to the lungs.

3) The oxygenated blood then returns to the left side of the heart.

Explanation:

4 0
3 years ago
The scientists mapping the SNPs in the human genome noticed that groups of SNPs tended to be inherited together, in blocks known
Over [174]

Answer:

SNPs have shown that only 0.1 % of DNA sequences are different in the human genome between different individuals, thereby all the inherited phenotypic variation observed in our species is associated with only 0.1 % of differences at the genome level  

Explanation:

Haplotypes are block-like sequences of DNA that are inherited together due to low recombination rates. Moreover, single-nucleotide polymorphism (SNP) mapping is a very useful methodology used to map the site of SNP mutations (i.e., SNP variants). In this regard, it has been observed that there are approximately 10 million common SNPs in the human genome. These SNPs contribute to the wide range of phenotypic variation observed in human populations for different traits (e.g., eye color, hair, weight, height, etc). Moreover, researchers have determined that SNPs can be clustered into haplotypes, thereby haplotypes can be accurately sampled by as few as approx. 300,000 selected SNPs, which are sufficient to represent all of the genetic variation across different human genomes.

5 0
3 years ago
Why is soil important to plants?
Elena-2011 [213]

Answer:

D-all of the above

Explanation:

The answer is D because....

  • Step one, It is not A Because although the statement is true it is not the best answer to fit the question. The soil does provide nutrients but it also does more, it provides temperature control, anchorage for the plant, and  the soil contains oxygen in it to help the plant grow.
  • Step two, lets look at B it provides them with water. Although this is true like A, it does more than provide them with water. It provides them a medium for growth.
  • Step three, So this answer is not correct because based on the option choices for option D all of the above is correct. It provides them a medium for growth to the plants likings.
  • Step four. This is correct because all of the above are true and best explain why soil is important to plants.
8 0
3 years ago
Read 2 more answers
What explains the diffrence in traits between all living organisms remember it begins with v​
larisa [96]

Answer:

Variation explains the difference in traits between all living organisms.

Explanation:

Without variation it would be pretty impossible to notice any "differences" in traits, especially between living organisms.

8 0
3 years ago
First identify the gametes. use pink labels to identify the male and female gamete types and white labels to identify the gamete
Lady bird [3.3K]
I found the whole exercise on the internet. Attached is the scheme with labels for the gametes, f2 generation, and respective frequencies.

For the gametes position, on the left pink square on the male gametes side you should put a capital G, <span>and on the right pink square on the male gametes side you should put a small g, as</span> the only two possible offsprings that are showing is "GG" under the left male gamete and "gg" under the right male gamete. On the top pink square on the female gametes side you should put a capital G, and on the bottom pink square on the female gametes side you should put a small g, as the only two possible offsprings that are showing is "GG" on the same line as the top female gamete and "gg" on the same line as the bottom female gamete.
As for the frequencies of the gametes, you should put the white label that marks 1/2 by the side of each gamete.
Related to the F2 generation, the top right and bottom left pink squares should have the label with a capital G and small g - "Gg" which reflects the combination of the male gamete on its line with the female gamete also on its line.
As for the frequencies of the progeny, each of the genotypes formed from the union of the gametes should have by the side the white label that marks 1/4.
The totals would be that GG is 1/4, Gg is 1/2 (1/4+1/4), and gg is also 1/4.

6 0
3 years ago
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