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NEET-UG Biology

Chromosome theory, linkage and recombination — practice questions

10 questions in the bank on this idea. Below are 10 of them, exactly as they appear in a test.

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  1. Question 1 · difficulty L1 · recall

    Exchange of segments between non-sister chromatids of homologous chromosomes:

    • A. crossing over
    • B. translation
    • C. transcription
    • D. segregation only
  2. Question 2 · difficulty L1 · recall

    Genes located close together on the same chromosome tend to show:

    • A. independent assortment always
    • B. complete dominance
    • C. polyploidy
    • D. linkage
  3. Question 3 · difficulty L3 · understanding

    Frequency of recombination between gene pairs on same chromosome as a measure of the distance between genes to map their position on chromosome, was used for the first time by

    • A. Sutton and Boveri
    • B. Alfred Sturtevant
    • C. Henking
    • D. Thomas Hunt Morgan
  4. Question 4 · difficulty L3 · understanding

    In meiosis, crossing over and exchange of genetic material between homologous chromosomes are catalyzed by the enzyme

    • A. Polymerase
    • B. Phosphorylase
    • C. Recombinase
    • D. Transferase
  5. Question 5 · difficulty L3 · understanding

    Given below are two statements : one is labelled as Assertion (A) and the other is labelled as Reason (R). Assertion (A) : Mendel's law of independent assortment does not hold good for the genes that are located closely on the same chromosome. Reason (R) : Closely located genes assort independently. In the light of the above statements, choose the correct answer from the options given below :

    • A. Both (A) and (R) are correct and (R) is the correct explanation of (A)
    • B. Both (A) and (R) are correct but (R) is not the correct explanation of (A)
    • C. (A) is correct but (R) is not correct
    • D. (A) is not correct but (R) is correct
  6. Question 6 · difficulty L3 · understanding

    The recombination frequency between the genes a & c 5&, b & c is 15%, b & d is 9%, a & b is 20%, c & d is 25% and a & d is 29%. What will be the sequence of these genes on a linear chromosome?

    • A. a, d, b, c
    • B. d, b, a, c
    • C. a, b, c, d
    • D. a, c, b, d
  7. Question 7 · difficulty L3 · understanding

    The chromosomal theory of inheritance was proposed by

    • A. Robert Brown
    • B. Thomas Morgan
    • C. Sutton and Boveri
    • D. Gregor Mendel
  8. Question 8 · difficulty L3 · understanding

    Now-a-days it is possible to detect the mutated gene causing cancer by allowing radioactive probe to hybridise its complimentary DNA in a clone of cells, followed by its detection using autoradiography because:

    • A. mutated gene does not appear on photographic film as the probe has complementarity with it
    • B. mutated gene partially appears on a photographic film
    • C. mutated gene completely and clearly appears on a photographic film
    • D. mutated gene does not appear on a photographic film as the probe has no complementarity with it
  9. Question 9 · difficulty L3 · understanding

    Experimental verification of the chromosomal theory of inheritance was done by

    • A. Sutton
    • B. Mendel
    • C. Morgan
    • D. Boveri
  10. Question 10 · difficulty L4 · analysis

    Two genes lie very close together on the same chromosome. Compared with genes far apart on that chromosome, what is most likely?

    • A. They show a higher recombination frequency
    • B. They assort independently in every meiosis
    • C. Stronger linkage and less recombination
    • D. They can never be inherited together

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