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.
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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.
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.
The daughter's father would have to have been colour blind, and the mother would need the inheritive gene from her father (the mother doesn't nessecarily need to show it, just have a colourblind father) in order for a female to end up actually colourblind. However, it's extremely rare.
Through the X chromosome, usually from a mother, (whom does not show any signs of colour blindness, yet she is a CARRIER of the X chromosome) passed down to son. Males usually get this because they only posses ONE X, in their XY life.
Males inherit the gene from their mothers.
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.
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It depends. If the child is male, the person to pass the trait on must be the mother. She may be a hybrid or color-blind herself for her to be capable of doing this. If the child is female, the father must be color-blind in addition to the mother being a carrier. Both have to donate the recessive gene to their daughter.
Women can not be colorblind, only men. For questions like these a punnett square is useful. Men can not carry the colorblind trait, but women can. I know this is kind of confusing. When a carrier ( a woman with the color blind trait) has children with a man ( color blind or not) her kids will have 50% chance of having that trait. If its a girl, she will be the carrier. If its a boy, he will have the colorblind trait. SO TO ANSWER YOUR QUESTION: Theoreticaly, 1 of the daughters will be the carrier, and the son will have a 50% chance of being colorblind. Women can be colorblind, its just rare. About every 6400 women one is colour blind and with men, every 80 men 1 is colour blind.
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)
The colorblind woman can pass the allele to all her children including sons and daughters but the daugthers will only be carriers for the trait whereas the sons will produce the trait. In order for the daughter to express the trait they would need the allele not only from the mother but from the father also. I just took an exam on this and got it right.
The expected phenotypic ratio for their offspring is 1:1, with a 50% chance of being color blind (male with the X-linked recessive trait) and a 50% chance of having normal color vision. This is because the daughter is a carrier of the recessive allele, which can be passed on to her offspring regardless of the father's color vision status.
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.
It is possible. There can be traits transferred from the grand-parents or great-grandparents which come up in the childs generation.
50%. 1 of the two male offspring will definately be color blind. Do a punnett square with the father having normal vision and the mother being a carrier.
Yes, it is possible. Color blindness is usually caused by a genetic mutation on the X chromosome. If both parents are carriers of the mutated gene, they can pass it on to their offspring, resulting in a color blind son.