The only possible outcome is EeWw, which will express the dominant genes but carry the recessive ones.
They get one chromosome from each parent, but since the parents all have matching chromsomes in this case then it doesn't matter which one they get. Since one parent has EE, E is the only one that can be passed on. Since the other has ee, they can only pass on e. Therefore, the child can only possible have Ee, as they get one from each parent.
There is a 50% chance of a homozygous dominant and a 50% chance of a heterozygous.
All of their children are expected to be heterozygous for the trait (Tt), which means they would be tall (dominant phenotype). The recessive trait for being short would only manifest if both copies of the gene were recessive.
There are two forms of Homozygous inheritance: Homozygous Dominant, and Homozygous Recessive. In order for two parents that are Homozygous to produce a Heterozygous offspring, one of them MUST be Homozygous Dominant, and the other MUST be Homozygous Recessive.
They are the same
A homozygous genotype refers to having two identical alleles for a particular gene. It can be either homozygous dominant (two dominant alleles, such as AA) or homozygous recessive (two recessive alleles, such as aa).
False because a living thing that shows a dominant trait can not be homozygous recessive. If it is homozygous recessive it will show recessive trait. A living thing that shows dominant trait may be homozygous dominant or hetrozygous.
The name of the gene pair that consists of a dominant and recessive allele, i.e. (Xx) will be a heterozygous allele. In this situation, the characteristics of the dominant characteristic will mask that of the recessive allele. People have have a heterozygous genotype may be carriers for diseases that reside on the recessive allele.
Homozygous dominant individuals have two copies of the dominant allele for a trait, homozygous recessive individuals have two copies of the recessive allele, and heterozygous individuals have one copy of each allele. Homozygous dominant and heterozygous individuals will express the dominant trait, while homozygous recessive individuals will express the recessive trait.
The homozygous dominant individual can only pass on the dominant allele and the homozygous recessive individual can only pass on the recessive allele, therefore all offspring will be heterozygous and have the dominant phenotype.
Homozygous means "same" so a homozygous recessive trait would be a same [with parents] trait that is not the stronger trait which is dominant. Dominant is stronger showing trait, recessive is weaker trait. If you are dealing with Punnett squares then tt is homozygous recessive and TT is homozygous dominant. Hope this helped...
Homozygous dominant for two dominant genes or homozygous recessive for two recessive genes.
Homozygous dominant individuals have two identical dominant alleles for a particular gene, resulting in the expression of the dominant trait. Homozygous recessive individuals have two identical recessive alleles, resulting in the expression of the recessive trait.
There is a 50% chance of a homozygous dominant and a 50% chance of a heterozygous.
heterozygous recessive
The phenotypes of attached and unattached earlobes do not fit neatly into the Mendelian theory of two alleles for one trait, and there is a continuum of earlobe phenotypes. That said, unattached earlobes are a dominant trait, so if the individual is homozygous for unattached earlobes, all of her offspring will have the unattached phenotype, even if some or all of them are heterozygous.
A gene pair that consists of 2 dominant or 2 recessive alleles is considered homozygous dominant or homozygous recessive.
All of their children are expected to be heterozygous for the trait (Tt), which means they would be tall (dominant phenotype). The recessive trait for being short would only manifest if both copies of the gene were recessive.