In the case of co-dominance, the F1 generation resembles:
1. | Dominant parent | 2. | Recessive parent |
3. | Both the parents | 4. | None of the parents |
Genes that code for a pair of contrasting traits or slightly different forms of the same gene are known as:
1. | Alleles | 2. | Loci |
3. | Cistrons | 4. | Introns |
What is the mode of inheritance of phenylketonuria?
1. | Autosomal recessive | 2. | Autosomal dominant |
3. | Sex linked recessive | 4. | Sex linked dominant |
Which of the following is not a feature of Down’s Syndrome?
1. | It is caused by a non-disjunction in an autosome. |
2. | The affected individual has a trisomy of chromosome 21. |
3. | The affected individual has a characteristic simian palmar crease. |
4. | The mental development of the affected individual is normal. |
What is F2 phenotypic ratio in a dihybrid cross?
1. | 1 : 1 | 2. | 3 : 1 |
3. | 9 : 3 : 3 : 1 | 4. | 1 : 1 : 1: 1 |
In true breeding, the allelic pair of genes are:
1. | Homologous | 2. | Linked |
3. | Stable | 4. | Homozygous |
The expression of only one of the parental characters in a monohybrid cross in the F1, the expression of both in the F2 and the proportion of 3:1 obtained at the F2 can be explained by:
1. Law of Dominance
2. Law of segregation
3. Law of Independent Assortment
4. Two-factor interaction
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 |
Mutations that arise due to changes in a single base pair of DNA are called as:
1. | Chromosomal aberrations | 2. | Point mutations |
3. | Nonsense mutations | 4. | Frameshift mutations |
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. |