Answer:
- person’s <u>genotype</u> is their unique sequence of DNA. More specifically, this term is used to refer to the two alleles a person has inherited for a particular gene. <u>Phenotype</u> is the detectable expression of this genotype – a patient’s clinical presentation.
Explanation:
person’s phenotype results from the interaction between their genotype and their environment.
The connection between genotype and phenotype is not always clear-cut. This means that you may encounter disparities between your patient’s genomic test result and their clinical presentation. Similarly, the phenotype of patients with a given genetic condition may vary greatly even within families.
Answer:Greenhouse gases allow thermal energy to pass through the atmosphere and back out into space
Explanation:
The answer is B: no
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Answer:
C. It is a male with atleast one dominant allele
Explanation:
In the given pedigree, the two normal parents of the generation I have one daughter with the attached earlobe. Since the trait is recessive, the daughter should be homozygous recessive to express the trait. The genotype of the daughter (shaded circle in generation II) is "aa". To have a daughter with "aa" genotype, both the parents should have one copy of "a" allele. So, the genotype of both parents is "Aa".
In generation II, individual A is non-shaded square. Squares represent males in a pedigree. Since its not shaded, it does not have attached earlobe. Both the parents are heterozygous dominant for attached earlobes (Aa x Aa = 1/4 AA : 1/2 Aa : 1/4 aa). The genotype of this individual may be AA or Aa.
