The Formation of the Universe: Tutorial 26 of 51 E Save & E
? Question
Drag the tiles to the boxes to form correct pairs.
As you've learned, different objects in space emit different wavelengths of electromagnetic radiation. Use the chart to match
each of the following wavelengths to the correct region of the electromagnetic spectrum.
10-
10
10.
1013
Increasing Frequency (v)
109
10
109 10 10" (Hz)
10"
1014
1012
1010
10
Y rays
X rays
UV
IR
Long radio waves
Microwave FM JAM
Radio waves
10 10
1
10
TO
10-12
10
110
10
10
100
10
10'
10
109
2 (m)
Increasing Wavelength 0) ►
Visible spectrum
100
700
500
600
Increasing Wavelength() in nm

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Explanation:

busy and ni answers

answer; i believe the correct answer is ( proteins );

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.