TLS Online TPP Program

#Question id: 18899


Cobalt-57 is a radioactive element  Used as a tracer to diagnose 

#SCPH01 Biochemistry
  1. tumor irradiation
  2. thyroid disorders
  3. genetics research.
  4. pernicious anemia
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TLS Online TPP Program

#Question id: 4764

#SCPH12 I Genetics

Which of the following is the best example of overdominance?

TLS Online TPP Program

#Question id: 4765

#SCPH01 Biochemistry

The recessive mutant allele that causes cystic fibrosis is much more frequent in Caucasians population than in other world populations. Some scientists believe heterozygotes must have had a survival advantage during plagues such as cholera that occasionally swept through this population. What concept does this illustrate?

TLS Online TPP Program

#Question id: 4765

#SCPH12 I Genetics

The recessive mutant allele that causes cystic fibrosis is much more frequent in Caucasians population than in other world populations. Some scientists believe heterozygotes must have had a survival advantage during plagues such as cholera that occasionally swept through this population. What concept does this illustrate?

TLS Online TPP Program

#Question id: 4766

#SCPH01 Biochemistry

In soybeans, resistance to sudden death syndrome (SDS) is inherited as a dominant condition. In some cases, individuals that are not resistant to SDS (but whose parents were) can pass the trait on to their progeny. This is an example of which of the following?

TLS Online TPP Program

#Question id: 4766

#SCPH12 I Genetics

In soybeans, resistance to sudden death syndrome (SDS) is inherited as a dominant condition. In some cases, individuals that are not resistant to SDS (but whose parents were) can pass the trait on to their progeny. This is an example of which of the following?

TLS Online TPP Program

#Question id: 4767

#SCPH01 Biochemistry

Neurofibromatosis is a condition in humans which is generally inherited in a dominant fashion. Assuming this disorder is 90% penetrant, what is the chance that a single child born to a father with neurofibromatosis and a mother known not to carry the mutation will have the disorder?