TLS Online TPP Program

#Question id: 14979


Which is not true of mitochondria and chloroplasts?

#Unit 2. Cellular Organization
  1. They are found in all organisms.
  2. They contain DNA and 70S ribosomes.
  3. They are capable of performing protein synthesis.
  4. They generate ATP
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TLS Online TPP Program

#Question id: 12495

#Unit 8. Inheritance Biology

Haemophilia A is a severe coagulation disorder that shows X-linked recessive inheritance. Red-green colour blindness also shows X-linked recessive inheritance. A man with both haemophilia A and colour blindness is referred for genetic counseling. Assume that his partner is not a carrier of either of these conditions. Which of the following is correct?

TLS Online TPP Program

#Question id: 12496

#Unit 8. Inheritance Biology

A woman who has two brothers and a maternal uncle (her mother's brother) with non-specific X-linked mental retardation is referred for genetic counselling. There are no diagnostic tests available to help determine whether or not she is a carrier. Which of the following is correct?

TLS Online TPP Program

#Question id: 12497

#Unit 8. Inheritance Biology

In this pedigree A and B represent alleles at a marker locus closely linked to the disease locus. Affected individuals are shown as shaded. The disease status in III 1 is unknown. Which of the following is correct?

TLS Online TPP Program

#Question id: 12498

#Unit 8. Inheritance Biology

In this pedigree II 1 is affected with an autosomal recessive disorder. The disease status for II 2 and II 3 is unknown. A and B represent alleles at a locus which is tightly linked to the disease locus with recombination fraction of 0. On the basis of the linked marker genotypes II 2 can be told that: 


TLS Online TPP Program

#Question id: 12499

#Unit 8. Inheritance Biology

On the basis of the linked marker genotypes II 3 can be told that:


TLS Online TPP Program

#Question id: 12500

#Unit 8. Inheritance Biology

In this pedigree II 1 is affected with an autosomal recessive disorder. The disease status for II 2, II 3 and II 4 is unknown. A and B represent alleles at a locus which is tightly linked to the disease locus with recombination fraction of 0. On the basis of the linked markers II 2 can be told that: