🧬 Genetics & Heredity — Practice WorksheetBiology | NEET · CUET | FirstInTest
Q1. Mendel's law of segregation is also known as:
Q2. In a monohybrid cross Tt × Tt, the phenotypic ratio of the F₂ generation is:
Q3. A cross between a homozygous tall plant (TT) and a homozygous dwarf plant (tt) produces:
Q4. Colour blindness in humans is a:
Q5. The blood group system in humans is an example of:
Q6. Down syndrome is caused by trisomy of chromosome:
Q7. The chromosomal constitution of Turner syndrome is:
Q8. Crossing over occurs during which stage of meiosis?
Q9. In incomplete dominance, the F₂ phenotypic ratio of a monohybrid cross is:
Q10. The test cross is used to determine:
Q11. Sickle cell anaemia is caused by a point mutation in the gene coding for:
Q12. Linkage was first experimentally demonstrated by:
Q13. In a dihybrid cross between two heterozygous parents (RrYy × RrYy), calculate the expected phenotypic ratio and the number of offspring with both recessive traits out of 256 progeny.
Q14. A colour-blind man marries a carrier woman. Show the cross and determine the probability of their children being colour-blind.
Q15. In a population, the frequency of the recessive allele (q) for albinism is 0.1. Using the Hardy-Weinberg equation, calculate the frequency of carriers (heterozygotes) in the population.
Q16. Explain the inheritance pattern of ABO blood groups. A man with blood group A (heterozygous) marries a woman with blood group B (heterozygous). What are the possible blood groups of their children?
Q17. Differentiate between complete linkage and incomplete linkage. If two genes are 20 cM apart on a chromosome, what is the recombination frequency?
Q18. A plant with genotype AaBbCc is self-pollinated. If all three genes assort independently, how many different genotypes and phenotypes are possible in the offspring?
Q19. Explain the chromosomal theory of inheritance. How did Morgan's experiments with Drosophila provide evidence for sex-linked inheritance?
Q20. A couple has a child with phenylketonuria (PKU), an autosomal recessive disorder. Neither parent shows the disease. What are the genotypes of the parents? What is the probability that their next child will have PKU?