To determine the chances that her daughters will be carriers, we need to consider the inheritance pattern of the gene in question. If the trait is autosomal recessive, carrier mothers pass on one copy of the gene to each daughter, giving her a 50% chance of being a carrier. If the trait is X-linked, the probability will depend on the mother's genotype and whether the father is affected or a carrier. Without specific genetic information, it's difficult to provide a precise percentage.
torche carriers
Fleet Aircraft Carriers. (Fleet Carriers are a navy's largest carrier).
They were referred to as "Jeep" carriers .
USN had 3 carriers and 50 support vessels; IJN had 4 carriers, 7 battlehips and 150 support vessels.
I know the United States has 9 aircraft carriers. Rest of the world??
A male with hemophilia does in fact carry the genes and can pass them on to his daughters, so yes, some boys (if they have hemophilia) are carriers.
McLeod's Daughters - 2001 Second Chances 7-1 is rated/received certificates of: Netherlands:6
Your sons should be safe unless they get a spontaneous mutation causing hemophilia. (this is extremely rare and almost negligible, however can happen) Your daughters however will definitely be carriers and may have low factor levels as well (typically not as severe as the father). Any grandsons produced by your daughters would have a 50% chance of being hemophiliacs as well.
Males and females can be carriers, male carriers can only pass on to their daughters, they will be carriers as well have a premutation. Females can pass on to their sons or daughters, they will have the premutation or the full mutation.
The chances of inheriting muscular dystrophy from your parents largely depend on the specific type of muscular dystrophy and the inheritance pattern associated with it. For instance, Duchenne and Becker muscular dystrophies are X-linked recessive disorders, meaning that mostly males are affected and females can be carriers. If a mother is a carrier, there is a 50% chance of passing the gene to her sons, who would be affected, and a 50% chance for daughters to be carriers. Other types may follow different inheritance patterns, so genetic counseling is often recommended for families with a history of the condition.
If you are a carrier of hemophilia (which is common in females who have a hemophiliac father) and your husband does not have the condition, there is a 50% chance that your daughter will inherit the gene for hemophilia and be a carrier, but not actually have the condition herself. There is also a 50% chance she will not inherit the gene at all. If you have hemophilia, all of your daughters will be carriers, while your sons will not be affected.
Pick a job that is associated with aircraft would improve your chances of being on a carrier.
The chances of their son having hemophilia depend on several factors, including the specific type of hemophilia and the genetic status of the parents. Hemophilia A and B are X-linked recessive disorders, which means that if the mother is a carrier, there is a 25% chance with each pregnancy that a son will inherit the disorder. If the father has hemophilia, all daughters will be carriers, and none of the sons will be affected. Therefore, the likelihood varies based on the parents' genetic backgrounds.
No. Carriers are people that carry the gene for something but exhibit no phenotype for it. Since males have no extra copy to hide a recessive trait, they cannot be carriers for sex linked traits.Answ2. Followers of this question should consult say haemophilia in wikipedia.com.
Males who are carriers will pass on the gene to all of their daughters, they will be FX carriers. Females who have the premutation (50-200 CGG repeats) or full-mutation (over 200 CGG repeats) have a 50/50 chance of passing it on with each pregnancy. Now just because they pass it on doesn't mean the child will be affected (especially when it comes to girls, since girls have 2 X chromosomes, the other X may produce enough protein.)
carriers are a parent carrying the particular recessive gene for a disease but is not affected by that disease. However, its offspring will have that gene as dominant increasing its chances of being affected by that disease if the parent mates with another parent of the opposite gender who is also a carrier.
In genetics, if a colorblind gene is located on the X chromosome, all daughters in generation 2 would inherit this gene from their father, who carries the colorblind trait. Since daughters receive one X chromosome from each parent, they will inherit their father's X chromosome carrying the colorblind gene, while receiving a second X chromosome from their mother. This results in all daughters being carriers of the colorblind gene. If the mother is not a carrier, the daughters will not express colorblindness but will carry the gene.