A woman with 47 chromosomes due to three copies of chromosome 21 is characterized by -
- Superfemaleness
- Turner's syndrome
- Triploidy
- Down's syndrome
Previous year questions with solutions · 2000 – 2026
| Year | Questions | Papers | Avg / paper | Weightage |
|---|---|---|---|---|
| 2026 | 9 | 2 | 4.5 | 8.91% ↑60.4% |
| 2025 | 3 | 1 | 3 | 5.56% ↓47.2% |
| 2024 | 12 | 2 | 6 | 10.53% ↑32.6% |
| 2023 | 5 | 1 | 5 | 7.94% ↓13.4% |
| 2022 | 12 | 2 | 6 | 9.16% ↑174.8% |
| 2021 | 2 | 1 | 2 | 3.33% ↓58.3% |
| 2020 | 4 | 1 | 4 | 8.00% ↓15.2% |
| 2019 | 5 | 1 | 5 | 9.43% ↑29.7% |
| 2018 | 4 | 1 | 4 | 7.27% ↓17.1% |
| 2017 | 5 | 1 | 5 | 8.77% ↑12.1% |
| 2016 | 9 | 2 | 4.5 | 7.83% ↑42.2% |
| 2015 | 6 | 2 | 3 | 5.50% ↓23.6% |
| 2013 | 8 | 2 | 4 | 7.21% ↑48.5% |
| 2012 | 5 | 2 | 2.5 | 4.85% ↑16.5% |
| 2011 | 4 | 2 | 2 | 4.17% ↓58.3% |
| 2010 | 9 | 2 | 4.5 | 10.00% ↑40% |
| 2009 | 4 | 1 | 4 | 7.14% ↑96.4% |
| 2008 | 2 | 1 | 2 | 3.64% ↓62.9% |
| 2007 | 5 | 1 | 5 | 9.80% ↓35.7% |
| 2006 | 9 | 1 | 9 | 15.25% ↑20.1% |
| 2005 | 8 | 1 | 8 | 12.70% ↓12.7% |
| 2004 | 8 | 1 | 8 | 14.55% ↑12.7% |
| 2003 | 8 | 1 | 8 | 12.90% ↑3.2% |
| 2002 | 8 | 1 | 8 | 12.50% ↓18.1% |
| 2001 | 9 | 1 | 9 | 15.25% ↑64.7% |
| 2000 | 5 | 1 | 5 | 9.26% |
⚠ 1 of these questions are out of the current syllabus (marked on the question).
A woman with 47 chromosomes due to three copies of chromosome 21 is characterized by -
Haemophilia is more commonly seen in human males than in human females because -
Which of the following is not a hereditary disease?
A woman with normal vision, but whose father was colour blind, marries a colour blind man. Suppose that the fourth child of this couple was a boy. This boy -
A woman with 47 chromosomes due to three copies of chromosome 21 is characterized by
In a plant, red fruit (R) is dominant over yellow fruit (r) and tallness (T) is dominant over shortness (t). If a plant with RRTt genotype is crossed with a plant that is rrtt
A male human is heterozygous for autosomal genes A and B and is also hemizygous for hemophilic gene h. What proportion of his sperms will be abh?
Lack of independent assortment of two genes A and B in fruit fly Drosophila is due to
One of the parents of a cross has a mutation in its mitochondria. In that cross, that parent is taken as a male. During segregation of F2 progenies that mutation is found in -
A normal woman, whose father was colour-blind is married to a normal man. The sons would be :-
The recessive genes located on X-chromosomes in humans are always -
After a mutation at a genetic locus the character of an organism changes due to the change in :-
In a mutational event, when adenine is replaced by guanine, it is a case of -
Which one of the following traits of garden pea studied by Mendel was a recessive feature?
The genes controlling the seven pea characters studied by Mendel are now known to be located on how many different chromosomes?
Two crosses between the same pair of genotypes or phenotypes in which the sources of the gametes are reversed in one cross, is known as:
Pattern baldness, moustaches and beard in human males are examples of:
Which one of the following conditions though harmful in itself, is also a potential saviour from a mosquito borne infectious disease?
Down's syndrome is caused by an extra copy of chromosome number 21. What percentage of offspring produced by an affected mother and a normal father would be affected by this disorder?
In Drosophila, the sex is determined by:
Christmas disease is another name for :-
Which of the following is the example of pleiotropy ?
There are three genes a, b and c. The percentage of crossing over between a and b is 20%, b and c is 28% and a and c is 8%. What is the sequence of genes on chromosome?
On selfing a plant of F1 generation with genotype “AABbCC”, the phenotypic ratio in F2 generation will be
A gene is said to be dominant if : -
A diseased man marries a normal woman. They get three daughters and five sons. All the daughters were diseased and sons were normal. The gene of this disease is : -
Which of the following is a correct match -
Change in sequence of nucleotide in DNA is called as -
If a diploid cell is treated with colchicine then it becomes : -
Two non-allelic genes produce the new phenotype when present together but fail to do so independently then it is called