Mendel performed his experiments on:
Principles of Inheritance and Variation — Important Questions
SUMMARY: This chapter explores the fundamental principles of genetics, including how traits are inherited and the variations that occur in organisms.
KEY TOPICS: Mendel's laws of inheritance, monohybrid and dihybrid crosses, chromosomal theory of inheritance, sex determination, genetic disorders, pedigree analysis, mutation, genetic variation, linkage and recombination.
The law of segregation deals with:
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The phenotypic ratio in a typical dihybrid cross is:
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A condition in which a gene has more than two alleles is called:
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Down syndrome is due to:
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State Mendel's laws of inheritance.
Differentiate between incomplete dominance and codominance with examples.
Explain the inheritance of ABO blood group in humans.
What is sex linkage? Give an example.
What is pedigree analysis? Why is it important?
Discuss Mendel's monohybrid and dihybrid cross experiments with examples.
Explain the chromosomal theory of inheritance and its experimental basis.
Describe the inheritance of ABO blood group as an example of multiple allelism and codominance.
Explain the sex determination in humans, birds, and honey bees.
Discuss the various chromosomal disorders in humans with their causes and symptoms.
Compare complete dominance and incomplete dominance with the help of a table.
Assertion (A): Mendel's laws are universal.
Reason (R): They apply to all sexually reproducing organisms.
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Assertion (A): Hemophilia is a sex-linked disorder.
Reason (R): The gene for hemophilia is present on the X chromosome.
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Assertion (A): Mendel chose pea plant for his experiments.
Reason (R): Pea plants have many easily distinguishable characters and short life cycle.
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Assertion (A): Punnet square shows possible genotypes from a cross.
Reason (R): It helps in predicting the offspring of a genetic cross.
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Assertion (A): Sickle cell anaemia is an autosomal recessive disorder.
Reason (R): Two copies of the defective gene are needed for the disease to manifest.
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Statement 1: F1 generation in a monohybrid cross shows the dominant phenotype.
Statement 2: The recessive trait reappears in F2 generation in 1:3 ratio.
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Statement 1: Linked genes do not show independent assortment.
Statement 2: Linkage was first studied by T. H. Morgan in Drosophila.
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Statement 1: Klinefelter syndrome has 47 XXY chromosomes.
Statement 2: Such individuals show physical and mental abnormalities.
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Statement 1: Colour blindness is more common in males than females.
Statement 2: It is a recessive sex-linked trait carried on X chromosome.
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Statement 1: Crossing over leads to recombination of linked genes.
Statement 2: It contributes to genetic variation in offspring.
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The phenotypic ratio in F2 generation is:A3 tall : 1 dwarfB1 tall : 1 dwarfCAll tallDAll dwarf
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The genotype of F1 generation is:ATtBTTCttDTt and TT
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Explain Mendel's monohybrid cross and the laws derived from it.
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The possible blood groups of children from this cross are:AA and B onlyBO onlyCA B AB and ODAB only
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The ABO system illustrates:AMultiple allelismBCodominanceCBothDNeither
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Explain how the ABO blood group system illustrates multiple allelism and codominance.
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What is the phenotypic ratio observed in the F2 generation of Mendel's monohybrid cross?A1:2:1B3:1C9:3:3:1D1:1
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Explain Mendel's Law of Segregation in your own words.
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Which trait was dominant in Mendel's pea plant experiments?ADwarf heightBTall heightCGreen seed colorDWrinkled seed shape
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What is the phenotypic ratio of the F2 generation in a dihybrid cross?A3:1B9:3:3:1C1:1:1:1D1:2:1
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Define the principle of independent assortment.
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What were the parental genotypes used in Mendel's dihybrid cross example?ARrYy and RrYyBRRYY and rryyCRr and rrDRR and rr
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Study the table of human genetic disorders and answer:
| Disorder | Type | Cause |
|---|---|---|
| Sickle cell anaemia | Autosomal recessive | Substitution mutation in beta-globin |
| Hemophilia | X-linked recessive | Defective clotting factor VIII |
| Down syndrome | Chromosomal | Trisomy of chromosome 21 |
| Klinefelter syndrome | Chromosomal | 47 XXY |
| Turner syndrome | Chromosomal | 45 XO |
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Down syndrome is caused by:ATrisomy 21BTrisomy 18CXXYDXO
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Hemophilia is inherited as:AAutosomal dominantBAutosomal recessiveCX-linked recessiveDY-linked
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Differentiate between Mendelian and chromosomal disorders with examples.
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Predict the F2 phenotypic ratio for each Mendelian cross type.
| Cross type | F2 ratio |
|---|---|
| Monohybrid | ? |
| Test cross | ? |
| Incomplete dominance | ? |
| Dihybrid | ? |
Identify the type and cause of each human genetic disorder.
| Disorder | Type | Cause |
|---|---|---|
| Sickle cell anaemia | ? | ? |
| Hemophilia | ? | ? |
| Colour blindness | ? | ? |
| Down syndrome | ? | ? |
| Klinefelter syndrome | ? | ? |
| Turner syndrome | ? | ? |
Predict the possible blood groups of children for each parental ABO genotype combination.
| Parent 1 | Parent 2 | Possible blood groups |
|---|---|---|
| IAIA | IAIA | ? |
| IAi | IBi | ? |
| IBIB | ii | ? |
| IAIB | ii | ? |
Study the Punnett square of a dihybrid cross and answer:
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The F2 phenotypic ratio in a typical Mendelian dihybrid cross is:A3:1B1:2:1C9:3:3:1D1:1:1:1
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The 9:3:3:1 ratio illustrates Mendel's:ALaw of dominanceBLaw of segregationCLaw of independent assortmentDLaw of linkage
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Explain how the law of independent assortment leads to the 9:3:3:1 phenotypic ratio in F2.
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Based on the given diagram of a monohybrid cross, answer the following:
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What is the phenotypic ratio of the offspring in the F2 generation?A1:2:1B3:1C1:1D9:3:3:1
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Identify the dominant trait in the cross shown.
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Based on the given flowchart, answer the following:
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Which law states that allele pairs separate during gamete formation?ALaw of SegregationBLaw of Independent AssortmentCLaw of DominanceDNone of the above
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Explain the significance of the Law of Independent Assortment.
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Based on the given diagram of a dihybrid cross, answer the following:
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What is the expected phenotypic ratio in the F2 generation of a dihybrid cross?A3:1B9:3:3:1C1:1:1:1D1:2:1
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Identify the traits being studied in this dihybrid cross.
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