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Luba_88 [7]
3 years ago
15

You and other scientists have been able to get the same results after many experiments.what is proven data called

Biology
2 answers:
Ahat [919]3 years ago
5 0
A : It is a theory
It is proven by evidence but hypothesis is only a educational guess
zysi [14]3 years ago
3 0
The answer you a looking for is facts.

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Chromosome 21 figure D is the result of a process known as________
Softa [21]

Answer:

Chromosome 21 in figure D is the result of a process known as non-disjunction

Explanation:

Meiosis is the process of cell division that serves to obtain gametes, cells with exactly half the chromosome load of the species. This process involves the equal distribution of chromosomes in each daughter cell.

Non-disjunction is an alteration in the separation of the sister chromatids during meiosis, resulting in a gamete with non-separated sister chromatids, which when joined to a normal gamete can produce an organism with an extra chromosome.

In the karyotype shown in the photo, the non-disjunction in chromosome 21 produces a trisomy, a type of aneuploidy seen in Down syndrome.

Learn more:

Trisomy brainly.com/question/484286

8 0
3 years ago
How might the human body be compared to a car bicycle? Need help like now!
pashok25 [27]

Answer:

Like the human body, the bicycle relys on other things to keep moving. For example, in order for the bicycle to keep moving, the rider needs to have legs and be able to push the pedals foreward. In order to breath, the body needs to have lungs and those lungs depend on the heart to pump blood throughout the body. The lungs rely on the heart and your brething relys on your lungs. Hope this helped, brainliest always appreciated.

Explanation:

6 0
3 years ago
At birth, what is the average number of red blood cells per<br> mm of blood?
umka2103 [35]
Baby girls are 4.1mm
Baby boys a 3mm
7 0
3 years ago
Read 2 more answers
Which of these changes produces a chemical change?
Olin [163]

Answer:

b

dissolving is a chemical change

5 0
3 years ago
A woman who is a carrier for colour blindness (X-linked recessive) has children with a man who has normal colour vision. A. What
viva [34]

Answer:

Explanation:

The Genotype of the  woman is XCbXN

The man XNY

Since the allele for the color blindness is carried on one of the X -chromosomes of the  carrier mother, then  the male children will be color blind or carrier deopending on the defective gene they inherited. Since they will receive the defective or normal  allele from the  mothers,but the female will carriers or normal because they will inherit either defective allele or normal allele from the mother,but normal  X allele from the father.

Assuming the colorbind gene was inherited by One of the boys, and the girls take the defective genes

1. XNY vs XCbXN.Then the one of the  boys will be colorblind  and the one of  girls will be carriers. XNXCb, XNXN, XCbY,XNY  50 %

2.If the two boys take the effective genes from the mothers. and none of the girls take the defective alelle

Then the two boys will be colorblind and the girls will be carrries XcbY,XcbY and XNXN XNXN.(normal girls).

The proportions that will be  the females  since the girls can only take the defective allele from one of the normal and defective allele from the mother. Assuming the girls  take the defective allele from the mothers and take normal from the father,they will all  be carriers,since the X of the father is normal.

They can not have a color blind girl.Since the father is normal It takes two colorblind X-chromosome to give a girl.

5 0
3 years ago
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