The genotype of the unaffected children can be 1 of 2 different things. The genotype can be either completely dominant or heterogeneous.
If the parents both have the genotype Aa, their children could have the genotypes AA, Aa, or aa. The possible phenotypes for their children would be individuals with type A blood (AA or Aa genotype) or type O blood (aa genotype).
50% of the offspring will have the recessive genotype (cc) for hair color when one parent is Cc and the other parent is cc. This is because all their children will inherit one "c" allele from the parent with cc genotype.
If an AC genotype man and an AS genotype woman marry, each of their children has a 25% chance of being born with a sickle cell disease (SS genotype), a 50% chance of being a carrier like their parents (AS genotype), and a 25% chance of having a normal genotype (AA).
if a man were non- hemophiliac and he marries a woman whois homozygus for nan-hemophilia,give the possible genotypes of the children
The answer is genotype
The genotype of unaffected children is typically heterozygous (Aa) for a recessive genetic disorder where the unaffected individual carries one normal allele (A) and one mutated allele (a). Unaffected children would not exhibit any symptoms of the disorder because they have a normal allele to compensate for the mutated one.
The mother is genotype AB, the father is either genotype BO or BB. If the father is genotype BO, the children can be genotype AB, AO, BB, or BO. This results in children with phenotype blood types of: AB, A, or B. If the father is genotype BB, the children can be genotype AB, AB, BB, or BB. This results in children with phenotype blood types of: AB or B.
The mother is genotype AB, the father is either genotype BO or BB. If the father is genotype BO, the children can be genotype AB, AO, BB, or BO. This results in children with phenotype blood types of: AB, A, or B. If the father is genotype BB, the children can be genotype AB, AB, BB, or BB. This results in children with phenotype blood types of: AB or B.
The mother is genotype AB, the father is either genotype BO or BB. If the father is genotype BO, the children can be genotype AB, AO, BB, or BO. This results in children with phenotype blood types of: AB, A, or B. If the father is genotype BB, the children can be genotype AB, AB, BB, or BB. This results in children with phenotype blood types of: AB or B.
If only the mother has the thalassemia trait, each child has a 50% chance of inheriting the trait and becoming a carrier, and a 50% chance of being unaffected. The father’s genotype will determine the overall risk for the children. If the father does not have thalassemia or the trait, the children will only be carriers. However, if the father also carries the trait, there is a possibility of having children with thalassemia disease.
When a person with an "aa" genotype marries someone with an "ac" genotype, there is a risk of having offspring with various genotypes. The potential combinations for their children would be "aa," "ac," and "cc." If "a" represents a recessive allele associated with a genetic condition, there is a chance that children with an "aa" genotype could inherit that condition. Therefore, it is important for both partners to understand their genetic backgrounds to assess any health risks for their future children.
If the parents both have the genotype Aa, their children could have the genotypes AA, Aa, or aa. The possible phenotypes for their children would be individuals with type A blood (AA or Aa genotype) or type O blood (aa genotype).
The mother is genotype AB, the father is either genotype BO or BB. If the father is genotype BO, the children can be genotype AB, AO, BB, or BO. This results in children with phenotype blood types of: AB, A, or B. If the father is genotype BB, the children can be genotype AB, AB, BB, or BB. This results in children with phenotype blood types of: AB or B.
50% of the offspring will have the recessive genotype (cc) for hair color when one parent is Cc and the other parent is cc. This is because all their children will inherit one "c" allele from the parent with cc genotype.
If an AC genotype man and an AS genotype woman marry, each of their children has a 25% chance of being born with a sickle cell disease (SS genotype), a 50% chance of being a carrier like their parents (AS genotype), and a 25% chance of having a normal genotype (AA).
no they can only have children with as as as as
There are three alleles for blood type which can be represented by IA, IB, and i. A person with blood type O has the genotype ii. A person with blood type AB has genotype IAIB. If these two people produce children, those children will inherit one allele from each parent. They will therefore certainly inherit the i allele from their mother and either the IA or the IB from their father. The children with the genotype IAi will have type A blood, since the IA allele is dominant to the i allele. The children with the genotype IBi will have type B blood, since the IB allele is also dominant to the i allele.