Principles of Inheritance and Variation-1
Principles of Inheritance and Variation-1
132. In hybridisation, Tt × tt gives rise to the progeny of 138 One of the parents of a cross has a mutation in its
ratio mitochondria. In that cross, that parent is taken
(a) 2 : 1 (b) 1 : 2 : 1 as a male. During segregation of F2 progenies that
(c) 1 : 1 (d) 1 : 2. mutation is found in
(a) one-third of the progenies
133. A child of O-group has B-group father. (b) none of the progenies
of father will be (c) all the progenies
(a) IOIO (b) IBIB (d) fifty percent of the progenies.
(c) IAIB (d) IBIO.
139 What is the genetic disorder in which an
The contrasting pairs of factors in Mendelian crosses individual has an overall masculine development,
134 gynaecomastia and is sterile?
are called
(a) multiple alleles (b) allelomorphs (a) Down’s syndrome
(c) alloloci (d) paramorphs. (b) Turner’s syndrome
(c) Klinefelter’s syndrome
135. Pick out the correct statements. (d) Edward syndrome
(1) Haemophilia is a sex-linked recessive disease. 140. A man and a woman, who do not show any apparent
(2) Down’s syndrome is due to aneuploidy.
signs of a certain inherited disease, have seven
(3) Phenylketonuria is an autosomal recessive gene
children (2 daughters and 5 sons). Three of the
disorder.
sons suffer from the given disease but none of the
(4) Sickle cell anaemia is an X-linked recessive gene
disorder. daughters affected. Which of the following mode of
(a) (1), (3) and (4) are correct. inheritance do you suggest for this disease?
(b) (1), (2) and (3) are correct. (a) Sex-linked dominant
(c) (1) and (4) are correct. (b) Sex-linked recessive
(d) (2) and (4) are correct. - (c) Sex-limited recessive
(d) Autosomal dominant
136. Thalassemia and sickle cell anaemia are caused due
to a problem in globin molecule synthesis. Select the 141. On selfing a plant of F1-generation with genotype
correct statement. “AABbCC”, the genotypic ratio in F2-generation will
(a) Both are due to a quantitative defect in globin be
chain synthesis. (a) 3 : 1
(b) Thalassemia is due to less synthesis of globin (b) 1 : 1
molecules. (c) 9 : 3 : 3 : 1
(c) Sickle cell anaemia is due to a quantitative (d) 27 : 9 : 9 : 9 : 3 : 3 : 3 : 1.
problem of globin molecules.
(d) Both are due to a qualitative defect in globin 142.
chain synthesis. Which of the following pairs is wrongly matched?
(a) Starch synthesis in pea : Multiple alleles
(b) ABO blood grouping : Co-dominance
137. In the following human pedigree, the filled symbols (c) XO type sex determination: Grasshopper
represent the affected individuals. Identify the type (d) T.H. Morgan Linkage
of given pedigree.
(i)
: types of genetically different
143. How many different
gametes will be produced by a heterozygous plant
(ii) having the genotype AABbCc?
(a) Six (b) Nine
(iii) (c) Two (d) Four
145 Which of the following is suitable for experiment on 154. Represented here is the
inheritance pattern of a certain Female Male
linkage? father
mother
(a) aaBB × aaBB (b) AABB × aabb type of trait in humans. Which
(c) AaBb × AaBb (d) AAbb × AaBB one of the following conditions
could be an example of this Daughter Son
pattern?
146. Number of Barr bodies in XXXX female is (a) Phenylketonuria (b) Sickle cell anaemia
(a) 1 (b) 2
(c) Haemophilia (d) Thalassemia
(c) 3 (d) 4.
147
Sex is determined in human beings 155. Which one of the following conditions correctly
(a) by ovum describes the manner of determining the sex?
(b) at time of fertilisation (a) Homozygous sex chromosomes (ZZ) determine
(c) 40 days after fertilisation female sex in birds.
(d) seventh to eight week when genitals differentiate (b) XO type of sex chromosomes determine male
in fetus. sex in grasshopper.
148 A woman has an X-linked condition on one of her (c) XO condition in humans as found in Turner’s
syndrome, determines female sex.
X chromosomes. This chromosome can be inherited
(d) Homozygous sex chromosomes (XX)
by
produce male in Drosophila.
(a) only daughters
(b) only sons 156. Which one of the following conditions in humans
(c) only grandchildren is correctly matched with its chromosomal
(d) both sons and daughters. abnormality/linkage?
(a) Erythroblastosis fetalis - X-linked
149. If a colour-blind man marries a woman who
(b) Down’s syndrome - 44 autosomes + XO
is homozygous for normal colour vision, the
probability of their son being colour-blind is (c) Klinefelter’s syndrome - 44 autosomes + XXY
(a) 0 (b) 0.5 (d) Colour blindness - Y-linked
(c) 0.75 (d) 1.
157.
Sickle-cell anaemia is
150 Which one is the incorrect statement with regard to (a) caused by substitution of valine by glutamic
the importance of pedigree analysis? acid in the beta globin chain of haemoglobin
(a) It confirms that DNA is the carrier of genetic (b) caused by a change in a single base pair of DNA
information. (c) characterized by elongated sickle like RBCs
(b) It helps to understand whether the trait in with a nucleus
question is dominant or recessive. (d) an autosomal linked dominant trait.
(c) It confirms that the trait is linked to one of the
autosome. 158 Mongolian Idiocy due to trisomy in 21st chromsome
(d) It helps to trace the inheritance of a specific is called
trait. (a) Down’s syndrome
151. Lack of independent assortment of two genes A and (b) Turner’s syndrome
B in fruit fly Drosophila is due to (c) Klinefelter’s syndrome
(a) repulsion (b) recombination (d) Triple X syndrome.
(c) linkage (d) crossing over.
159. Haemophilic man marries a normal woman. Their
offspring will be
152. Segregation of Mendelian factors (no linkage, no (a) all haemophilic
crossing over) occurs during (b) all boys haemophilic
(a) anaphase I (b) anaphase II
(c) all girls haemophilic
(c) diplotene (d) metaphase I.
(d) all normal.
In Drosophila, the XXY condition leads to femaleness
160 whereas in human beings the same condition leads
153. A family of five daughter only is expecting sixth to Klinefelter’s syndrome in male. It proves
issue. The chance of its being a son is
(a) in human beings Y chromosome is active in sex
(a) zero (b) 25%
determination
(c) 50% (d) 100%. (b) Y chromosome is active in sex determination in
both human beings and Drosophila
(c) in Drosophila Y chromosome decides femaleness
(d) Y chromosome of man have genes for syndrome.
MOMENTUM Test Series for NEET - 2026