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Whitepunk [10]
3 years ago
5

I need help plz. It’s not the bottom left answer

Biology
1 answer:
zavuch27 [327]3 years ago
7 0
I think bottom right. Not 100% sure though
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What is the diploid chromosome number for your karyotype
LekaFEV [45]

Answer:

For example, a haploid human nucleus (i.e. sperm or egg) normally has 23 chromosomes (n=23), and a diploid human nucleus has 23 pairs of chromosomes (2n=46). A karyotype is the complete set of chromosomes of an individual.

Explanation:

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a rain forest primate called an aye-aye has a long middle finger. how did this structure develope over time?
amm1812
That's called evolution. I'm not sure exactly what it's asking, but I hope this helps you 
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a grown tiger began his life as a fertilized egg explain why a tiger looks so much different as an adult than it did as a single
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Because it grew so it changed over time.

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What is the purpose of the cell wall? What type of cell is it found in?
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Read 2 more answers
A couple planning their family are aware that through the past three generations on the husband's side a substantial number of s
Nesterboy [21]

Answer:

a) There are lots of genes on chromosome 1 could be affected, and the gametes could be imbalanced (missing segments of DNA or whole chromosomes)

b) Roughly 50%

c) No. I would advise that the couple undergo preimplantation genetic diagnosis, so that a zygote carrying the normal copy of chromosome 1 could be selected.

Explanation:

Chromosome 1 is one of the largest and most gene rich chromosomes. An inversion that covers 70% of its length would cover lots of genes.

While an inversion on its own would not seem problematic (as all the genes on the chromosome are still there), when it comes to meiosis, the sister chromatids would not be able to correctly align, and crossing over would further complicate this. It could also lead to unbalanced gametes missing entire parts of the chromosome. Therefore, there are likely numerous genes that will be affected and messed up by the inversion.

This could explain the high incidence of past still births, as if lots of genes are affected, and non-functional, the pregnancy would be rendered non-viable, or highly deleterious causing premature death.

b) There is a 50% chance of a child inheriting the defective copy of chromosome 1 (and 50% of a chance of them inheriting the normal chromosome 1. Therefore, there is likely a 50% chance that future offspring would be affected by defects

c) No. I would advise that the couple undergo preimplantation genetic diagnosis. In this, the couple undergoes in vitro fertilization (IVF). When embryos are produced through IVF, they can then be tested for the presence of the abnormal chromosome. Embryos will only be implanted into the mother if the normal chromosome 1 is present.

6 0
3 years ago
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