Pp x Pp yields PP, Pp, Pp, pp. PP is the only genotype which will cause the phenotypic expression of the gene - symptoms of PKU. Therefore the probability is 1/4 or 25%
It depends on the genotype of the childs other parent. If your partner is heterozygous as well then there is a 25% chance your child will be homozygous recessive. If they are homozygous dominant then none of your children will have the phenotype of the recessive trait. They will just possibly be carriers of the recessive allele.
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.
individuals that are heterozygous for alleles
Homozygous, heterozygous, dominant, recessive, co-dominant, incomplete dominant, alleles, multiple alleles, polygenic inheritance, test cross, Punnett squares, hybrids, carriers, ratios, percentages, locus.
It indicates a carior , which possess a recessive gene for disease but no symptoms of disease .
I don't know and don't care
Phenylketonuria (PKU) is inherited when both parents are carriers of the gene. Since it is a recessive gene, there is a 25% chance that any baby conceived by two people carrying the PKU gene will have PKU.
If you are heterozygous this means you carry both a dominant and recessive allele. if you are heterozygous for a recessive trait then you will have a dominant and recessive allele. example: let T represent tall and t represent short. a person with heterozygous for a recessive trait will have 'Tt'.
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.
It depends on the genotype of the childs other parent. If your partner is heterozygous as well then there is a 25% chance your child will be homozygous recessive. If they are homozygous dominant then none of your children will have the phenotype of the recessive trait. They will just possibly be carriers of the recessive allele.
The child will have the disorder, only if the recessive allele from both the parents is transferred to the child. Therefore, the probability is 1/4.
I don't know and don't care
I don't know and don't care
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.
genetically albinism is an autosomal recessive gene which in fact gives the child a 25% chance of inheriting the gene if both parents are carriers
A recessive trait can be masked by a dominant trait in individuals who are heterozygous. Thus, a majority of people may appear to display the dominant trait even if they are carriers of the recessive trait. Only when two carriers of the recessive trait have children together is there a chance for the recessive trait to become visible in the offspring.
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.