An individual affected with Turner’s Syndrome:

I: Is a female
II: Has 45 chromosomes
III: Has rudimentary ovaries

Of the above statements, the correct statements are:

1. Only I and II 2. Only I and III
3. Only II and III 4. I, II and III

Subtopic:  Sex Aneuploidy - Turner & Klinefelter Syndrome |
 86%
From NCERT

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.

Hints

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.


It is unfortunate that in our society women are blamed for producing female children and have been ostracised and ill-treated because:

1. The sex is determined by the type of sperm fertilizing the egg
2. The sex is determined by the type of egg fertilizing the sperm
3. The sex is determined by the hormones produced by the fetus
4. The sex is determined by God’s Will
Subtopic:  Sex Determination | Sex Determination: Further Considerations |
 89%
From NCERT

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.

Hints

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.


The units of inheritance according to Mendel were ‘factors’. Today these factors are known as:

1. Gametes 2. DNA
3. Genes 4. RNA
Subtopic:  Monohybrid Cross: Further Understanding |
 95%
From NCERT

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.

Hints

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.


advertisementadvertisement

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
Subtopic:  Dominance Deviation from Mendel: 1 |
 85%
From NCERT

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.

Hints

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.


The point mutation in sickle cell anaemia leads to a change in the codon. Identify the correct change:

1. UGA to UAA 2. GUG to GAG
3. GAG to GUG 4. UAA to UGA
Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 86%
From NCERT

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.

Hints

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.


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
Subtopic:  Monohybrid Cross: Further Understanding |
 95%
From NCERT

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.

Hints

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.


advertisementadvertisement

The two alleles of a gene pair are located on:

1. The same chromosome.
2. Different chromosomes.
3. Homologous sites on homologous chromosomes.
4. Homologous sites on heterologous chromosomes.
Subtopic:  Chromosomal Basis of Inheritance: Introduction |
 78%
From NCERT

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.

Hints

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.


Morgan, in his experiment on fruit flies, found that the genes white and yellow were very tightly linked and showed:

1.50 % recombination2.37.2 % recombination
3.12.5 % recombination4.1.3 % recombination

Subtopic:  Recombination & Gene Mapping |
 78%
From NCERT

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.

Hints

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.


What is the mode of inheritance of phenylketonuria?

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

Subtopic:  Mendelian Disorders |
 88%
From NCERT

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.

Hints

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.


advertisementadvertisement

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.
Subtopic:  Non - Disjunction & Aneuploidy |
 84%

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.

Hints

To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.