NOW. Colourblindness we will assume, is a Sex-Linked Disorder. Hence, the sex chromosomes are involved in determinig the phenotypes of the children. XY --male XX--female XbY--colourblind male XBXb --normal female Cross: (parents) Xby * XBXb F1 progeny/offspring XBXb, XbXb, XBY, XbY 50 % of the children will be colourblind. This is a very simple question. You also need to clarify within the question if it is sex linked or autosomal.
as previously stated, there is a 100% certainty that the son of a color blind mother will be color blind.
The chances of any daughter being color blind are a bit more complicated.
If the father is color blind, and the mother is as well, there is a 100% chance of the daughter being color blind too.
If the father is not, then the daughter of a color blind mother will not be color blind, though there is a 100% certainty that she will be a carrier, and so there is 50/50 chance that any of her sons will be (actually slightly more, if we account for the chance that her future partner may be color blind as well).
If we accept that the prevalence of color blindness in the male population is about 5%, then the likelihood of any daughter from a color blind mother and some random father is about 5% as well.
Yes the child will be red/green color blindif shown through a punnett square so its highly likely this will happen
There is a 100% chance their child/children will be red-green colorblind
The son will be color-blind. Color-blindness is a recessive trait found on the X-chromosome, and for someone to be color-blind all present X-chromosomes MUST have the recessive trait. Therefore, a son from a color-blind mother (who receives the trait from his mother on the X-chromosome) will always be color-blind, regardless of the state of the father (who can only give his son a Y-chromosome).
This is why color-blindness is more commonly found in men than in women, since men only require one X while women must have two X carrying the trait present. All of the daughters of this couple will be carriers of color-blindness, but will not be color-blind.
If a female who does not carry the color blindness gene has children with a color blind male, none of their offspring will be colorblind. Their daughters have a 50 percent chance of carrying the color blindness allele, and their sons will not carry it.
The probability of these two having a color blind son is close to 0 (though it is still possible). This is because color blindness is a recessive gene while normal vision is the dominant gene. Even though the son might not be color blind, he will still carry the color blind gene.
*The above answer is wrong....
The Probability of the son being color blind is 100%. The color blind gene is recessive and is located on the X chromosome. Mom has two X's and the dad: XY. The dad is not a carrier (and cant be) because he only has one X, and it can't carry the gene or he would express it.
The mom passes an X to her son and the dad passes his Y. The son has to have a color blind X because the mom is colorblind and the dad has no effect on whether or not his son is colorblind. Therefore, the son will be colorblind.
Woman carrier genotype = XCXc (where XC is the normal allele, and Xc is the affected allele)
Man who is not color blind must have genotype = XCY
Possible genotypes of children are:
XCXC , XCY, XcXC , and XcY
only one possible (out of 4) will be color blind (and only if they have a son). Therefore, there is a 25% chance that the child will be color blind.
50/50 because the child gets 26 chromozones from each parent so the chances are 50/50.
50%. It depends on which copy of the X chromosome the boy receives from the mother. Also, the father's color blindness doesn't matter at all for male children.
25% only they have a son
it depends on the husbands genotype, if it is a recessive gene (bb) then there is a 50 50 chance of either straight or curly hair. if the husbands straight hair is a heterozygous gene, then there is a 70% chance for either straight or curly hair.
yes the children would be cause they have purebred blood in them.....
Firstly, if the condition is recessive, both the man and the child with the condition must have the genotype tt. The mother must have the genotype Tt. This is because if she had TT, all of the children would be Tt and not have the condition. If she were tt, she would have the condition as well. Therefore if the father has tt and the mother has Tt, the other 3 children who do not have the condition must all have the genotype Tt. So: Mother - Tt Father - tt Affected child - tt Other children - Tt
25% for blood type O, 50% for blodd type AB, and 25% for A.
The man's genotype is CcFf. The woman's genotype is CcFf. These genotypes only apply if curly hair is dominant to straight hair. Freckles is dominant to no freckles. Also if a man who is heterozygous for both curly hair and freckles who then marries a woman with the same genotype.
50%
there is a 50% chance that the child will be colorblind. If it is a boy, it will be colorblind, but if it is a girl, it will only be a carrier. Mother's chromosome is XrXr and Father's Chromosome is XRY, which means the children's genotypes will be XRXr if girl and XrY if a boy.
50% of their children are expected to have a widow's peak. When a heterozygous male (Ww) with a widow's peak gene marries a female with a straight hairline (ww), their offspring have a 50% chance of inheriting the widow's peak gene from the father.
it depends on the husbands genotype, if it is a recessive gene (bb) then there is a 50 50 chance of either straight or curly hair. if the husbands straight hair is a heterozygous gene, then there is a 70% chance for either straight or curly hair.
Assuming that the man who has normal vision is homozygous for normal vision, the couple's daughter will either be homozygous for normal vision or heterozygous (normal vision but carrier for color blindness) for normal vision. In light of this, the couple's daughter will not be color blind.
Colorblindness is an X-linked recessive disorder. This means girls (who have the sex chromosomes XX) must have a colorblind X from dad and a colorblind X from mom. Boys only need to have one colorblind X to be colorblind because they have sex chromosomes XY (and have only 1 X). If the dad has it, he has the colorblind X. If the daughter has it, she must have gotten her mom's colorblind X. If the mom is colorblind, then every child they have will be colorblind. If the mom is not colorblind, then she must be a carrier - she must have 1 normal X and 1 colorblind X. Mom is either colorblind (with 2 colorblind Xs) or she is a carrier. Dad is definitely colorblind.
its called disgusting who marries there children unless you are in a different country but still eww
Yes, I think so. He marries Sakura Haruno and has kids.
In the Epilogue, Harry marries Ginny and has three children. Hermione marries Ron and they have one child.
Yes, Hermione marries Ron Weasley. Their two children are named Rose and Hugo Weasley.
Yes. He marries Hermione and they have Rose and Hugo Weasley.
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