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Different chromosomes can be easily identified in a karyotype.

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Al Leuschke

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βˆ™ 10y ago

Depending on the type of karyotype, you can tell what type of organism it is, if it has 23 pairs then you would know it is a human because humans have 46 chromosomes, one half from your mom and one half from your dad, making 23 pairs. Another thing you can tell is the organism has any gene disorders, like the 21 trisomy, or having an extra 21 chromosome, and causes Down syndrome. And the last thing you can determine is the sex or gender of the organism having 2 X's or XY.

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Karyotypes show the number and appearance of an individual's chromosomes. They can help identify genetic disorders, chromosomal abnormalities, and gender.

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βˆ™ 13y ago

Different chromosomes can be easily identified in a karyotype.

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chromatids, sister chromatids, centromere, homologous pairs, and chromosomes.

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the gender of the child

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Q: What two things do karyotypes show?
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When during mitosis are karyotypes made?

Karyotypes are made during metaphase of mitosis when the condensed chromosomes are lined up on the metaphase plate. At this stage, the chromosomes are most condensed and easily identifiable for analysis.


The most obvious way the karyotypes of a sister and brother look different?

The most obvious difference in the karyotypes of a sister and brother would be the sex chromosomes. A sister would typically have two X chromosomes (XX) and a brother would have one X and one Y chromosome (XY). This difference in sex chromosomes would be clearly visible when examining their karyotypes.


Do karyotypes change over time?

No, a person's karyotype does not change over time. It remains constant throughout their life. Karyotypes are unique genetic profiles that are determined by an individual's chromosomal makeup and are established at conception.


What is bimodal karyotype?

A bimodal karyotype is a chromosomal arrangement characterized by having two distinct sets of chromosome numbers in a population or individual. This can be due to variations such as aneuploidy or polyploidy, leading to two distinct peaks when chromosomes are counted. An example is Down syndrome (Trisomy 21), where individuals have an extra copy of chromosome 21, resulting in a bimodal karyotype.


Are Karyotypes pictures of the homologous chromosomes arranged in pairs?

Yes, a karyotype is an ordered display of an individual's chromosomes, showing them arranged in pairs based on their size and structure. Karyotypes are often used to identify genetic disorders and abnormalities by examining the number and structure of chromosomes.

Related questions

What are the karyotypes of diabetes?

there are no karyotypes of diabetes


What are shown on a karyotypes?

Karyotypes show a visual representation of an individual's chromosomes arranged by size, shape, and banding pattern. They can be used to detect genetic abnormalities, such as extra, missing, or rearranged chromosomes. Karyotypes are helpful in diagnosing genetic disorders and assessing chromosomal abnormalities.


An analogy is a comparison of two things in order to show ways in which they are?

Analogy is a comparison of two things in order to show how they are similar. An analogy compares two like things.


What clues to the presence of certain genetic disorders can be seen in a karyotypes?

-Extra, missing or damaged chromosomes could show the presence of genetic disorders.


How might karyotypes be useful to doctors?

Doctors can use karyotypes to determine the sex of an individual. They can also use karyotypes to determine whether an individual has an abnormal number of chromosomes or noticeable chromosomal mutations, such as large deletions, additions, or translocations.


When during mitosis are karyotypes made?

Karyotypes are made during metaphase of mitosis when the condensed chromosomes are lined up on the metaphase plate. At this stage, the chromosomes are most condensed and easily identifiable for analysis.


What process is responsible for abnormal karyotypes?

Abnormal karyotypes can result from processes such as chromosomal mutations, errors during meiosis or mitosis, exposure to mutagens, or genetic disorders. These processes can lead to changes in chromosome number (aneuploidy) or structure (translocations, deletions, duplications), resulting in abnormal karyotypes.


Why do karyotypes always show chromosomes at the point when cell division is about to occur?

They show chromosomes at the point when cell division is about to occur because the chromosomes are condensed and aligned which makes it easy to tell if there are the correct number and configurations of the chromosomes.


What are karyotypes found in?

A karyotype is the characteristic chromosome complement of a eukaryote species. In essence karyotypes describe your chromosomes. for more information go to http://en.wikipedia.org/wiki/Karyotype


What are micrograph images used to study chromosomes called?

karyotypes


How do you draw a data table to record observations of karyotypes?

you dont


The most obvious way the karyotypes of a sister and brother look different?

The most obvious difference in the karyotypes of a sister and brother would be the sex chromosomes. A sister would typically have two X chromosomes (XX) and a brother would have one X and one Y chromosome (XY). This difference in sex chromosomes would be clearly visible when examining their karyotypes.