include the information listed below.
Include a thesis statement that clearly and concisely states the paper’s purpose.
Describe the single-trait genetic disorder you selected.
State whether it is a dominant or recessive disorder.
State whether it is sex-linked or autosomal recessive disorder.
State the genotype or possible genotypes of a person with the disorder.
Relate the genotype to phenotype of a person with the disorder and define phenotype.
Describe the symptoms, diagnosis, prognosis.
Discuss treatment options, including medicines/alternative treatments.
Describe incidence rate or statistics.
Describe what can be done to reduce the incidence rates.
Include a Punnett square of the parents that could produce offspring with the disorder.
Include the ratios of each genotype and phenotype produced by the cross.
Within your discussion of the above items, include definitions for the terms listed below:
single-trait genetic disorder,
dominant and recessive,
sex-linked trait and autosomal disorder, genotype and phenotype, and heterozygous and homozygous.
include an introduction, a body with a review and discussion of literature, and a conclusion
Include a thesis statement that clearly and concisely states the paper’s purpose.
Describe the single-trait genetic disorder you selected.
State whether it is a dominant or recessive disorder.
State whether it is sex-linked or autosomal recessive disorder.
State the genotype or possible genotypes of a person with the disorder.
Relate the genotype to phenotype of a person with the disorder and define phenotype.
Describe the symptoms, diagnosis, prognosis.
Discuss treatment options, including medicines/alternative treatments.
Describe incidence rate or statistics.
Describe what can be done to reduce the incidence rates.
Include a Punnett square of the parents that could produce offspring with the disorder.
Include the ratios of each genotype and phenotype produced by the cross.
Within your discussion of the above items, include definitions for the terms listed below:
single-trait genetic disorder,
dominant and recessive,
sex-linked trait and autosomal disorder, genotype and phenotype, and heterozygous and homozygous.
include an introduction, a body with a review and discussion of literature, and a conclusion
