The genotype is homozygous recessive or the recessive trait is on the X chromosome and has no corresponding allele on the Y chromosome.
Phenotypes are the traits expressed by the genotype. So, for blood type, a person can have A and i alleles (genotype). However, in the phenotype, since i is recessive, only the A will be expressed, and the person will have an A blood type.
heterozygous
genotype
See excellent related answers below.
Either analyzing the DNA sequence (which you probably don't have a lab to do it in) or breeding the organism and use a PUNNET SQUARE to determine if they are purebred. (don't try the breeding experiment on humans.)
Phenotypes are the traits expressed by the genotype. So, for blood type, a person can have A and i alleles (genotype). However, in the phenotype, since i is recessive, only the A will be expressed, and the person will have an A blood type.
Phenotypes are the traits expressed by the genotype. So, for blood type, a person can have A and i alleles (genotype). However, in the phenotype, since i is recessive, only the A will be expressed, and the person will have an A blood type.
I think no. It's caused by a recessive gene so if a person has albinism their genotype can only be recessive, recessive ---> AA (small a small a or whatever you call it). No other genotype will mean that person has Albinism, like if it has at least one big A, that means it's just a carrier of albinism.
heterozygous
genotype
See excellent related answers below.
Either analyzing the DNA sequence (which you probably don't have a lab to do it in) or breeding the organism and use a PUNNET SQUARE to determine if they are purebred. (don't try the breeding experiment on humans.)
B. Bill is recessive for height and dominate for hair color.
The genotype of a person with CF is cc. The genotype of a carrier of a CF mutation is Cc.
In some cases but not others. Certain alleles can be dominant, which means that they will dictate the phenotype should there be a clash of alleles in the genotype. Other alleles can be recessive, which means you'd need both of these alleles in these genotype in order for it to dictate the phenotype. This means that if a person's phenotype represents a dominant trait, we cannot be certain what their genotype is. If, however, it represents a recessive trait, we know that their genotype must be the recessive allele twice.
There is no single answer to this question.First, some definitions. PHENOTYPE is how the trait is physically displayed in the person, so the parents in this case have the phenotypes O and A. GENOTYPE is the pair of genes that a person carries that determines their phenotype. A RECESSIVE gene is one "trumped" by a DOMINANT gene in the genotype; for blood typing, O is the recessive gene and A and B are dominant. For a person to show the recessive phenotype, they must carry BOTH recessive genes; so, a person with type O must carry two O genes, genotype "OO".OK, now for our situation. The O parent has genotype OO, as explained above, and so can ONLY pass on the O gene. The type A parent, however, can have genotype AA or AO. Because the A gene is dominant, with the AO genotype the parent is still type A but can pass on EITHER the A gene or the O gene. The child can therefore end up with phenotype AO and be type A or OO and be type O. If exactly one-half of people with type A blood have genotype AA and one-half have AO, the probability of this child being type A is 75%.For the Rh factor (positive and negative), positive is the dominant trait and negative is recessive. The A- parent must be genotype -/- and can only pass on the - gene. The O+ parent can be +/+ or +/- and can pass on either gene, same situation as above. Again, if people with Rh type positive are split exactly 50/50 in genotypes, this child has a 75% chance of being positive.
b. bill is recessive for his height and something something thanks, Jose A Hernandez