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31 Years NEET Previous Year Questions: Heredity And Variation - 2


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25 Questions MCQ Test Biology Class 12 | 31 Years NEET Previous Year Questions: Heredity And Variation - 2

31 Years NEET Previous Year Questions: Heredity And Variation - 2 for NEET 2023 is part of Biology Class 12 preparation. The 31 Years NEET Previous Year Questions: Heredity And Variation - 2 questions and answers have been prepared according to the NEET exam syllabus.The 31 Years NEET Previous Year Questions: Heredity And Variation - 2 MCQs are made for NEET 2023 Exam. Find important definitions, questions, notes, meanings, examples, exercises, MCQs and online tests for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 below.
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31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 1

The incorrect statement with regard to Haemophilia is :

[NEET 2013]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 1

Haemophilia is sex linked recesive disease in which a simple protein that is a part of protein cascade involved in clotting of blood is affected. Due to this, in an affected individual a simple cut will result in non stop bleeding.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 2

Which of the following statements is not true of two genes that show 50% recombination frequency?

[NEET 2013]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 2

Tightly linked genes show more linkage then crossing over.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 3

Which Mendelian idea is depicted by a cross in which the F1 generation resembles both the parents?

[NEET 2013]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 3

In Co-dominance F1 generation resemble both the parents. Ex : Blood group inheritance.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 4

If two persons with ‘AB’ blood group marry and have sufficiently large number of children these children could be classified as ‘A’ blood group: ‘AB’ blood group: ‘B’ blood group in 1 : 2 : 1 ratio. Modern technique of protein electrophoresis reveals presence of both ‘A’ and ‘B’ type proteins in ‘AB’ blood group individuals. This is an example of :              

[NEET 2013]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 4

ABO blood group system in human beings is an example of codominant, dominant recessive and multiple alletes. Blood groups are controlled by the gene I located on 9th chromosome that has 3 multiple alleles, out of which any two are found in a person. In codominance both gene express it self completely.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 5

A test cross is carried out to

[2012M]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 5

A test cross, first introduced by Gregor Mendel, is used to determine if an individual exhibiting a dominant trait is homozygous or heterozygous for that trait. It takes place between F1 - Generation and recessive parent.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 6

Which one of the following is a wrong statement regarding mutations?

[2012M]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 6

Change in single base pair of DNA is also a type of mutations called point mutations. It is a type of mutation that causes the replacement of a single base nucleotide with another nucleotide of the genetic material, DNA or RNA. For example, a point mutation is the cause of sickle cell disease.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 7

A normal-visioned man whose father was colour¬blind, marries a woman whose father was also colour-blind. They have their first child as a daughter. What are the chances that this child would be colour-blind?

[2012]

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 8

A certain road accident patient with unknown blood group needs immediate blood transfusion. His one doctor friend at once offers his blood.What was the blood group of the donor?

[2012]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 8

Blood group O acts as universal donor.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 9

Which one of the following conditions of the zygotic cell would lead to the birth of a normal human female child ?

[2011M]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 9

Two X chromosomes would lead to the birth of normal human female child.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 10

The unequivocal proof of DNA as the genetic material came from the studies on a

[2011M]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 10

Bacteriophage was used by Hershey and Chase to prove DNA as genetic matterial.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 11

Test cross in plants or in Drosophila involves crossing

[2011M]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 11

In test cross, genotype of an organism showing dominant phenotype is determined by crossing it with homozygous recessive genotype.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 12

A person with unknown blood group under ABO system, has suffered much blood loss in an accident and needs immediate blood transfusion. His one friend who has a valid certificate of his own blood type offers blood donation without delay. What would have been the type of blood group of the donor friend?

[2011]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 12

Type Oblood group is considered the universal donor blood group. It can potentially be transfused to any patient regardless of their blood type. In emergency situation, this type of blood can be given to the patient.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 13

Mutations can be induced with :

[2011]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 13

Mutation can be induced by gamma radiation.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 14

When two unrelated individuals or lines are crossed, the performance of F1 hybrid is often superior to both parents. This phenomenon is called:

[2011]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 14

Heterosis or hybrid vigor occurs when two unrelated individuals or lines are crossed, the performance of F1 hybrid, which is often superior to both is parents.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 15

Which one of the following conditions correctly describes the manner of determining the sex in the given example?

[2011]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 15

In grasshopper the males lack a Y-sex chromosome and have only an X-chromosome. They produce sperm cells that contain either an X chromosome or no sex chromosome, which is designated as O.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 16

Infectious proteins are present in:

[2010]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 16

Infections proteins are rich in prions. Prions are made of proteins without nucleic acid. It is the causal agent of scrapie disease of sheep.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 17

Select the correct statement from the ones given below with respect to dihybrid cross.

[2010]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 17

Linkage is the inheritance of genes of same chromosome together and capacity of these genes to retain their parental combination in subsequent generation. The strength of linkage between two genes is inversely proportional to the distance between the two. This means, two linked genes show higher frequency of recombination if the distance between them is higher and lower frequency if the distance is smaller.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 18

The genotype of a plant showing the dominant phenotype can be determined by :

[2010]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 18

Test cross is the cross of an individual with an individual having recessive phenotype. It is used to determine the genotype of a plant showing the dominant phenotype, that means to determine whether the individual exhibiting dominating characters are homozygous or heterozygous.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 19

Which one of the following can not be explained on the basis of Mendel’s Law of Dominance?

[2010]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 19

According to Mendel’s law of Dominance, out of two contrasting allelomorphic factors only one expresses itself in an individual. The factor that expresses itself is called dominant while the other which has not shown its effect in the heterozygous individual is termed as recessive. The option (c) in the given question cannot be explain-ed on the basis of law of dominance. It can only be explained on the basis of Mendel’s Law of independent assortment, according to which in a dihybrid cross, the two alleles of each character assort independently of the alleles of other character and separate at the time of gamete formation.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 20

Point mutation involves:

[2009]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 20

A point mutation is a simple change in one base of the gene sequence. This is equivalent to changing one letter in a sentence, such as this example, where we change the ‘e’ in cat to an ‘h’: Original: The fat cat ate the wee rat. Point Mutation: The fat hat ate the wee rat.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 21

Select the incorrect statement from the following:

[2009]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 21

Baldness is a sex influenced trait. The dominance of alleles may differ in heterozygotes of the two sexes.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 22

Sickle cell anaemia is:

[2009]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 22

The correct option is Option B.

Haemoglobin is made of four polypeptide chains two α-chains which are 141 amino acid long and two β-chains which are 146 amino acids long. Sickle cell anaemia is due to inheritance of a defective allele coding for β-globin. It results in the transformation of HbA into HbS in which glutamic acid (Glu) is replaced by valine (Val) at sixth position in each of two β globin chain of haemoglobin. The substitution of amino acid in the globin protein results due to the single base substitution at the sixth codon of the beta globin gene from GAG to GUG.

So, it is caused by the substitution of valine by glutamic acid in the beta globin chain of haemoglobin.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 23

The genetic defect - Adenosine deaminase (ADA) deficiency may be cured permanently by:

[2009]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 23

By introducing bone marrow cells producing ADA into cells at early embryonic stages, the genetic defect adenosine deaminase (ADA) deficiency may be cured permanently. It is due to mutation.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 24

Study the pedigree chart given below: What does it show?

[2009]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 24

The chart shows the inheritance of a condition like phenylketonuria as an autosomal recessive trait. Parents’ needs to be heterozygous as two of their children are known to be sufferer of the disease. It cannot be recessive sex linked inheritance because then the male parent would also be sufferer.

31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 25

Which one of the following conditions in humans. is correctly matched with its chromosomal abnormality/linkage?

[2008]

Detailed Solution for 31 Years NEET Previous Year Questions: Heredity And Variation - 2 - Question 25

Klinefelter's syndrome is a genetic disorder affecting men in which an individual gains an extra X chromosome, so that the usual Karyotype of XY is replaced by one of XXY. Symptoms of  Klinefelter's syndrome  named after us physician H.P. Klinefelter, include female characteristics (such as breast enlargement). 

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