People receive a total of 46 genotypes from their parents.
The parents have normal genotypes, because Klinefelter's syndrome is not inherited.
If both parents carry the gene for albinism, which is an autosomal recessive disorder, there is a 25% chance their child will be affected by albinism, a 50% chance the child will be a carrier like the parents, and a 25% chance the child will neither have albinism nor be a carrier. Therefore, there is a 75% chance that their child will not have albinism, either being a carrier or completely unaffected.
Yes. If either parent is a carrier of the gene that causes albinism then their child becomes a carrier as well. It is only when both parents have the gene for albinism that the child is born with this disorder.
The parents can pass on only the alleles of their genotypes to their offspring. Therefore, the offspring genotypes and phenotypes are dependent solely upon the alleles inherited from the parents.
A Punnett square is used to lay out the possible genotypes of offspring based on the genotypes of the parents being bred. From this, the probabilities of certain phenotypes and genotypes can be determined.
That depends entirely on the genotypes of the parents.
That depends entirely on the genotypes of the parents.
Albinism is a genetic condition that is inherited when both parents carry a specific gene mutation. This mutation is passed down through generations in an autosomal recessive pattern, meaning that both parents must pass on the mutated gene for a child to have albinism.
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
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