First child will always prevail from being SS. Some even have AA, but most of the time. Its AS.
No probability. Neither parent has an "A" for the child to inherit to make an "AB".
50% AA and 50% Aa
yes, as it's genetic
If both parents are carriers of the sickle cell trait (genotype AS), there is a 25% chance that their child will inherit the sickle cell disease (genotype SS). Each parent has one normal hemoglobin allele (A) and one sickle cell allele (S), which means the possible combinations for their child are AA, AS, and SS. Therefore, the probability of the child being affected by sickle cell disease is 25%. If both parents have sickle cell disease (genotype SS), then all children will also be affected (100%).
To determine the probability that Anna and Bill's child will have A type blood, we first consider their genotypes. Anna, with A type blood, could have either AA or AO genotype, while Bill, with AB type blood, has genotype AB. If Anna is AA, all their children will be A type. If she is AO, there’s a 50% chance of A type blood (AO) and a 50% chance of O type blood (OO). Therefore, the probability that their child will have A type blood ranges from 50% to 100%, depending on Anna's genotype.
The genotype of the man is A negative/O negative inheriting the A neg from his mother and O negative from his father. [Father's genotype is B positive/O negative. Mother's genotype is B positive/A negative.]
The woman would have genotype AO (IAIA) for blood type A, the man would have genotype BO (IBIB) for blood type B, and their child with blood type O would have genotype OO (ii). The child inherited one O allele from each parent.
A genotype is decided from two alleles. One of these alleles comes from the father, and one comes from the mother. Thus it should be clear that the genotype can be different from both parents. For instance, suppose the father has genotype AA, and the mother has genotype aa. In this case, the child will have genotype Aa, which neither parent has.
Yes, if both parents are AO genotype there is a 25% chance of the parents producing a type O child. Since both parents are Rh positive the probability of an Rh positive child in at least 75%.
Child's genotype would be homozygous recessive alleles (nn) and parents would both have heterozygous dominant alleles (Nn).
Assuming that each parent is a carrier for cystic fibrosis (has the genotype Ff), the probability that their second child will develop cystic fibrosis is one fourth. The probability doesn't change with the number of children they have. For each pregnancy, the chance that the child will have cystic fibrosis (have the genotype ff) is exactly the same.
No, a parent with AS and AA genotype cannot give birth to a child with AC genotype. The parent can only pass on either the A allele or the S allele to their child, resulting in genotypes of either AA or AS.