When there is a change in the chromosome number such that the changes number is not an exact multiple of base number [haploid number], the condition is called as:

1. Euploidy 2. Aneuploidy
3. Aberration 4. Non-disjunction

Subtopic:  Non - Disjunction & Aneuploidy |
 78%
From NCERT
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On self-pollinated a tall F2 plant, the progeny can be:

1.Tall only2.Dwarf only
3.Intermediate in height4.Tall and Dwarf

Subtopic:  Monohybrid Cross: 1 |
 85%
From NCERT
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Mutations that arise due to changes in a single base pair of DNA are called as:

1.Chromosomal aberrations2.Point mutations
3.Nonsense mutations4.Frameshift mutations

Subtopic:  Mutation |
 93%
From NCERT
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The inheritance of IA and IB allele exhibit:

1. Complete dominance 2. Incomplete dominance
3. Co-dominance 4. Lethality
Subtopic:  Dominance Deviation from Mendel: 1 |
 92%
From NCERT
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In humans, the mechanism of sex determination is:

1. XX – XY; male heterogamety
2. XX – XY; female heterogamety
3. XX – XO; male heterogamety
4. XX – XO; female heterogamety
Subtopic:  Sex Determination | Sex Determination: Further Considerations |
 95%
From NCERT
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When Morgan hybridised yellow-bodied, white-eyed females to brown-bodied, red-eyed males and intercrossed their F1 progeny, the F2 ratio deviated very significantly from the 9:3:3:1 ratio. This can be attributed to the fact that:

1. The genes are located on the X and Y chromosomes.
2. Fruit fly has abnormal chromosomes.
3. The genes are located on the X chromosome.
4. The genes exhibit incomplete dominance.
Subtopic:  Chromosomal Basis of Inheritance: Introduction | Chromosomal Basis of Inheritance: Further Considerations | Understanding Linkage |
 66%
From NCERT
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In a dissimilar situation, the unit factor that expresses itself is called as:

1. Dominant 2. Recessive
3. Epistatic 4. Hypostatic
Subtopic:  Monohybrid Cross: 1 |
 85%
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The number of alleles, the genotypic combinations, and phenotypes in the ABO system are respectively:

1. 3, 6 and 4 2. 3, 4 and 6
3. 2, 3 and 4 4. 2, 3, and 6
Subtopic:  Dominance Deviation from Mendel: 1 |
 86%
From NCERT
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Thalassemia is inherited as a/an ____________ condition.

1.Autosomal recessive2.Autosomal dominant
3.Sex linked recessive4.Sex linked dominant

Subtopic:  Mendelian Disorders: Thalassemia |
 87%
From NCERT
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The family pedigree of Queen Victoria shows a number of haemophilic descendants as she was:

1. Affected by the disease
2. Carrier for the disease
3. Did not carry the allele for hemophilia
4. Was not a queen
Subtopic:  Mendelian Disorders: Hemophilia |
 91%
From NCERT
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