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 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.
no they can only have children with as as as as
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).
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.
The chances of an AC genotype and an AS genotype having children with an SS or SC genotype depend on the inheritance patterns of sickle cell traits. The AC parent can pass on either the A or C allele, while the AS parent can pass on either the A or S allele. The possible combinations for their children are AA, AC, AS, and CS, meaning that neither SS nor SC offspring can occur from these parents. Thus, the chances of having SS or SC children are zero.
I think it's genotype...