Wiki User
∙ 10y agoYou might need to indicate what the disorder is.
Wiki User
∙ 10y agothere are half the chance of a female and half the chance of male so probabilty in both cases is 1/2
51%
No- they do almost ALL the hunting.
the colorblindness is usually not activited in a female body but is usually seen in male
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.
The mother has a 50% chance of passing the defective recessive gene to her daughters who will be carries of the disorder (like their mother).
When a female is heterozygous i.e. she possess one allele of disease , she is called carrier .
Usually female.
A female with one copy of the allele will be a carrier, but not have the disorder.
A carrier for hemophilia is a female who carries the genetic mutation for hemophilia on one of her X chromosomes, but does not exhibit symptoms of the condition herself. Carriers can pass on the gene mutation to their children, resulting in hemophilia in male offspring. Testing can confirm carrier status.
50/50 chance
Hemophilia is passed down from mother to son. It is extremely rare for a woman to have hemophilia. It is necessary, though, for a woman to be a carrier of the disorder for her son to acquire this disorder. Females have two X chromosomes whereas males only have one. When a boy is born, he takes one X chromosome from his mother and one Y chromosome from his father. Therefore, he can only get hemophilia through his mother. Example One: Mother(Carrier)+Father(Non-Affected)=50% chance of their son acquiring the disorder and 50% chance of their daughter being a carrier. Example Two: Mother(Non-Affected)+Father(Hemophiliac)=All sons will be non-affected and all daughters will be carriers.
The offspring will have a 50% chance of being a carrier female (XHX), a 50% chance of being a healthy male (XHY), and a 0% chance of having hemophilia. Hemophilia is inherited as an X-linked recessive trait, meaning the father passes on the Y chromosome to sons, who will not inherit the X-linked disorder.
Yes but there is only a 12.5 percent chance of it happening
Hemophilia is a genetic disorder that is usually inherited in an X-linked recessive pattern. It can appear to skip a generation when a carrier female passes the gene to her son, who then expresses the disorder. However, it doesn't truly skip a generation as the gene is passed on in each generation.
Using the Punnet square, if the male is xY and the female is XX, where x = recessive and X = dominant, then males get the disease since they only have 1 x chromosome. Females can be carriers, Xx, or have the disease..xx, or not at all XX..so X X (female none carrier)x Xx XxY XY XY(male carrier)Leaves you with 100 percent chance of daughters being carriers, and 100 Percent chance for sons being healthy none carriers....
Anyone can be a carrier of a recessive genetic disorder (as long as it is not associated with the sex chromosomes) no matter what their gender since "carrier" refers to an individual that is heterozygous for the recessive allele and therefore phenotypically normal. Specifically, sexlinked genetic disorders can be "carried" by a heterozygous female but males (having only one X chromosome) cannot. Males will either be free of the defective gene or be affected.