All daughters are normal, half the sons are color blind.
The above answer is incorrect. Half of the daughters are color blind and half of the sons are color blind. Since the father always donates color blindness, it is up to the mother in each case (in the son's case, the father is irrelevant) to determine if the child is color blind or not. Since she is a carrier, the chance is 50-50.
X' = color blindnessX'X'-- X --X'Yis a cross that could lead to a color blind female as the mother is homozygous recessive and the father's X chromosome is the recessive color blind trait.
50% (apex)
if the child is a boy, 0%. if it's a girl, either 100% if the trait is dominant in the father or 50% if it is recessive. there is also the possibilty of the daughter having it but just being a carrier (has the disease but no signs of it)
Bcoz one chromosome comes from mother which is always X chromosome carries characteristics from mother and the second chromosome comes from father that may be X or Y, which carries characters from father.
Turner's syndrome is caused by a missing or incomplete X chromosome. Since the gene for red-green color blindness is located on the X chromosome, if the girl inherited the X chromosome carrying the red-green color blindness gene from her father, she could have the condition even though her father has normal vision. Her mother would be a carrier of the gene, but with two X chromosomes, she likely does not exhibit red-green color blindness herself.
his mother because color blindness is a sex-linked trait that is found on the X chromosome, which is inherited from the mother, as opposed to the Y chromosome, which is inherited from the father. So a male can only inherit the gene for color blindness from his mom.
50%
The probability of a child being color blind depends on the parents' genetic makeup. If the mother is a carrier of the color blindness gene located on the X chromosome and the father does not carry the gene, the chances are 0% for a daughter and 50% for a son to inherit color blindness. If the father is color blind and the mother is a carrier, the chances are 50% for a daughter and 50% for a son to inherit color blindness.
X' = color blindnessX'X'-- X --X'Yis a cross that could lead to a color blind female as the mother is homozygous recessive and the father's X chromosome is the recessive color blind trait.
Boys have one X and one Y chromosome. Color blindness is found on the X chromosomes. Since boys will always get their X chromosome from their mother and their Y chromosome from their father, father's can never pass on red/green color blindness to their son's. However, since father's do pass their X chromosome to their daughters, they can pass on the trait to their daughters. In this case, daughters have two X chromosomes (one from their mother and one from their father), so they will NOT have red/green color blindness unless they received the defective gene from their mother AND their father. This is the reason that color blindness is 9 times more common in boys than girls.
Color blindness is a sex-linked trait that is carried on the X chromosome. Since males inherit their single X chromosome from their mother, if the mother carries the allele for color blindness, her son will inherit it and be colorblind. Females need two copies of the allele to be colorblind, so they can be carriers without exhibiting the trait.
50% (apex)
A positive with highest probability
The probability of getting curly hair depends on whether your parents do or not. Hair genes are decided by the mother. So, if the mother has curly hair, more than likely the offspring will as well. If the father has curly hair and the mother does not, the probability is considerably lowered.
25% to be B.
Color blindness is typically inherited in an X-linked recessive pattern. This means that a son inherits his X chromosome from his mother and his Y chromosome from his father. Therefore, regardless of the mother's phenotype, she is the parent responsible for passing on the X chromosome that may carry the gene for color blindness, while the father contributes a Y chromosome. If the mother is a carrier or affected, there is a chance for the son to be color blind.
If the mother is a carrier of the colorblind gene (XcX) and the father has normal color vision, the probability of their child being colorblind is 50%. This is because the child has a 50% chance of inheriting the Xc chromosome from the mother and developing colorblindness.