The answer would be skeletal markers and DNA analysis.
Skeletal markers are often used to identify the biological gender of skeletal remains. The most commonly used skeletal markers can be observed in the skull and in the pelvic bone.However, the accuracy of his method is limited to adults only the differences between male and female skeletal markers usually become visibly only after maturation.
DNA analysis is more widely uses nowadays because with the technology of today, laboratories can now detect and X and Y chromosome-specific sequences, which help them identify the biological gender.
Color blindness is a recessive x-linked trait in humans. In a family where the mother is color-blind, and the father is normal, the probability of their having a color-blind son is 100%.
Color blindness is a recessive x chromosome liked recessive disease which is more prone in males than in females. As the mother is color-blind she has both the alleles of colorblindness while the father is normal with both x chromosome and y chromosome normal.
So if the parents have a boy, he will always receive an x chromosome with colorblindness gene from the mother and a normal y chromosome from the father always. Thus, the probability of having a colorblind boy will be 100%.
To know more about colorblindness refer to the link below
brainly.com/question/2094919
#SPJ4
Answer:
Diabetes is a condition in which your blood glucose, often known as blood sugar, is abnormally high. Your main source of energy is blood glucose, which comes from the food you eat. Insulin, a hormone produced by the pancreas, aids glucose absorption into cells for use as energy.
Hope this helps!
