Ans.
Albinism shows a genetic disorder, which is characterized by absence of coloration or pigmentation in individuals. It is an autosomal recessive disorder that transmits from parents to their offspring, when offspring receives both the mutated copies of gene responsible for albinism.
For a genetic disorder, dominant or wild type allele is represented by capital letter, such as 'A', while recessive or mutated allele is represented by small letter, 'a'. As 4th picture is representing male and female gametes with recessive alleles (a) , the resulting zygote will have both recessive alleles for albinism (aa), '4th zygote will develop into an albino child.'
Answer: In people with type AB blood, both A and B proteins are expressed on the surface of red blood cells equally.
Explanation:
Answer:
By reversing that trend, pharmacogenomics helps to refine the focus of treatment and makes drugs more effective and less toxic. ... Thus, many potential drugs which may be lost due to the effects on the outliers in a study can be retained when pharmacogenomic study is used in the future.
Explanation:
A non polar compound hope this helps
