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प्रश्न
Briefly mention the contribution of T. H. Morgan in genetics.
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उत्तर
Thomas Hunt Morgan (1866-1945), an American geneticist and Nobel Prize winner in 1933, is recognised as the “Father of Experimental Genetics” for his work on and discovery of linkage, crossing over, sex linkage, criss-cross inheritance, linkage maps, gene mutability, and so on. He is known as the fly man of genetics because he used fruit flies (Drosophila melanogaster) as research subjects in experimental genetics. His book “The Theory of Gene” primarily recognised genetics as a distinct discipline within biology. In 1910, he identified linkage and discriminated between linked and unlinked genes. Morgan and Castle’s (1911) “Chromosomal Theory of Linkage” argued that genes are located on chromosomes and ordered in a linear order. Morgan and Sturtevant (1911) discovered that the frequency of crossover (recombination) between two connected genes is exactly proportional to their distance. 1% recombination is equivalent to 1 centi Morgan (cM) or 1 map unit. He researched sex-linked inheritance and discovered a white-eyed male Drosophila in a red-eyed population, proving that the gene for eye colour is located on the X chromosome. The man passed genes on the X chromosome to the daughter, whereas the son received genes on the X chromosome from the mother. It is known as criss-cross inheritance.
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संबंधित प्रश्न
If centromere is situated in the middle of the chromosome, it is called ________.
(a) Metacentric
(b) Acrocentric
(c) Submetacentric
(d) Telocentric
What is gene pool?
Sketch and label the structure of chromosome.
How many chromosomes do drones of honey bees possess?
Who had proposed the chromosomal theory of inheritance?
Explain the types of chromosomes on the basis of position of centromere.
Choose the correct options of the following question:
Study the given monohybrid cross:

A test cross for this Fj will be:
Answer the following question.
Compare in any three ways the chromosomal theory of inheritance as proposed by Sutton and Bovery with that of experimental results on pea plant presented by Mendel.
Genes G S L H are located on the same chromosome. The recombination percentage is between L and G is 15%, S and L is 50%, H and S are 20%. The correct order of genes is
If you cross dominant genotype PV/PV male Drosophila with double recessive female and obtain F1 hybrid. Now you cross F1 male with double recessive female.
What is the possible genotype in the F2 generation?
Telocentric chromosome differs from acrocentric chromosome in that ____________.
Which of the following is a primary constriction?
Read the following statements regarding 'X and Y' chromosomes and select the correct option.
P - Due to presence of large amount of euchrornatin X chromosome is genetically more active.
Q - Due to presence of small amount of heterochromatin Y chromosome is genetically more active.
Chromosomal theory of inheritance was put forth by ______
Which of the following does NOT agree with chrotnosomal theory of inheritance?
Extranuclear inheritance occurs in ______.
Two or more independent genes present on different chromosomes which determine nearly same phenotype are called ______.
Mendel’s work was rediscovered by three scientists in the year ______.
How many types of gametes would be produced if the genotype of a parent is AaBB?
Which of the following statements indicates parallelism in genes and chromosomes?
- They occur in pairs.
- They segregate during gamete formation.
- They show linkage.
- Independent pairs segregate independently.
A couple has two daughters. What is the probability that the third child will also be a female?
There was a mix-up at the hospital after a fire accident in the nursery division. Which of these children belong to the parents?

During mitosis, chromosomes distribution to the daughter cell is ______.
Who postulated the 'Chromosomal theory of inheritance'?
Discuss in detail the contributions of Morgan and Sturvant in the area of genetics.
Experimental verification of the chromosomal theory of inheritance was done by ______.
Which of the following is sex chromosomal disorder?
According to the Chromosomal Theory of Inheritance, what are the specific positions on chromosomes where genes are located called?
In what year did Walter Sutton publish the formal paper "The Chromosomes in Heredity" that linked Mendel's laws to chromosome behaviour?
