If two persons '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
codominance
incomplete dominance
partial dominance
complete dominance
Which Mendelian idea is depicted by a cross in which the F1 generation resembles both the parents?
Incomplete dominance
Law of dominance
Inheritance of one gene
Codominance
The incorrect statement with regard to haemophilia is
it is a sex-linked disease
it is a recessive disease
it is a dominant disease
a single protein involved in the clotting of blood effected
F2 generation in a Mendelian cross showed that both genotypic and phenotypic ratios are same as 1:2:1. It represents a case of
dihybrid cross
monohybrid cross with complete dominance
monohybird cross the incomplete dominance
Which one of the following conditions correctly describes the manner of determining the sex in the given example?
XO type of sex chromosomes determine male sex in grasshopper
XO condition in humans as found in Turner syndromee, determines female sex
Homozygous sex chromosomes (XX) produce male in Drosophila
Homozygous sex chromosomes (ZZ) determine female sex in birds
Mutations can be induced with
IAA
ethylene
gama radiations
infra red radiations
Which one of the following cannot be explained on the basis of Mendel's Law of Dominance?
The discrete unit controlling a particular character is called a factor
Out of one pair of factors one is dominant, and the other is recessive
Alleles do not show any blendings and both the characters recover as such in F2 generation.
Factors occur in pairs
The genotype of a plant showing the dominant phenotype can be determined by
test cross
pedigree analysis
back cross
ABO blood groups in humans are controlled by the gene I. It has three alleles — IA, IB and i. Since there are three different alleles, six different genotypes are possible. How many phenotypes can occur?
Three
One
Four
Two
Select the correct statement from the ones given below with respect to dihybrid cross.
Tightly linked genes on the same chromosome show higher recombinations
Genes far apart on the same chromosome show very few recombinations
Genes loosely linked on the same chromosome show similar recombinations as the tightly linked ones
Tightly linked genes on the same chromosome show very few recombinations.
Which one of the following symbols and its representation, used in human pedigree analysis is correct?
= Marriage between relatives
= Unaffected male
= Unaffected female
= Male affected
Sickel cell anaemia is
an autosomal linked dominant trait
caused by substitution of valine by glutamic acid in the β-globin chain of haemoglobin.
caused by a change in base pair of DNA
characterized by elongated sickle like RBCs with a nucleus.
Point mutation involves
insertion
change in single base pair
duplication
deletion
Select the incorrect statement from the following
linkage is an exception to the principle of independent assortment in heredity
galactosemia is an inborn error of metabolism
small population size results in random genetic drift in a population
baldness is a sex limited trait
Which one of the following condition in human is correctly matched with its chromosomal abnormality/linkage?
Klinefelter's syndrome—44 autosomes + XXY
Colourblindness —Y-linked
Erythroblastosis foetalis— X-linked
Down syndrome—44 autosomes + XO
A human male produces sperms with the genotypes AB, Ab, aB and ab pertaining to two diallelic characters in equal proportions. What is the corresponding genotype of this person ?
AaBb
AaBB
AABb
AABB
In the hexaploid wheat, the haploid (n) and basic (x) numbers of chromosomes are:
n = 7 and x = 21
n = 21 and x = 21
n = 21 and x = 14
n = 21 and x = 7
Inheritance of skin colour in humans is an example of :
chromosomal aberration
point mutation
polygenic inheritance
Which of the following genotype express gametes?
TtRrAa
TtRA
ATRr
NMLr
Two genes R and Y are located very close on the chromosomal linkage map of maize plant. When RRYY and rryy genotypes are hybridised, then F2 segregation will show :
higher number of the recombinant types
segregation in the expected 9 : 3 : 3 : 1 ratio
segregation in 3 : 1
higher number of the parental types
A common test to find the genotype or hybrid is by :
crossing of one F2 progeny with male parent
crossing of one F2 progeny with female parent
studying the sexual behaviour of F1 progenies
crossing of one F1 progeny with recessive parent
In pea plants, yellow seeds are dominant to green. If heterozygous yellow seeded plant is crossed with a green seeded plant, what ratio of yellow and green plants would you expect in F1 generation ?
50 : 50
9 : 1
1 : 3
3 : 1
Which one of the following is the most suitable, medium for culture of Drosophila melanogaster ?
Moist bread
Agar agar
Ripe banana
Cow dung
Phenotype of an organism is the result of :
mutations and linkages
cytoplasmic effects and nutrition
environmental changes and sexual dimorphism
genotype and environmental interactions.
In which mode of inheritance do you expect more maternal influence among the offspring ?
Autosomal
Cytoplasmic
Y-linked
X-linked
How many different kinds of gametes will be produced by a plant having the genotype AABbCC ?
Nine
Which one of the following is an example of polygenic inheritance ?
Flower colour in Mirabilis jalapa
Production of male honey bee
Pod shape in garden pea
Skin colour in humans
In Mendel's experiments with garden pea, round seed shape (RR) was dominant over wrinkled seeds (rr), Yellow cotyledon (YY) was dominant over green cotyledon (yy). What are the expected phenotypes in the F2 generation of the cross RRYY x rryy ?
Only round seeds with green cotyledons
Only wrinkled with yellow cotyledons
Only wrinkled seeds with green cotyledons
Round seeds with yellow cotyledons and wrinkled seeds with yellow cotyledons.
Test cross involves :
crossing between two geneotypes with recessive trait
crossing between two F1 hybrids
crossing the F1 hybrid with a double recessive genotype
crossing between two genotypes with dominant trait
Cri-du-chat syndrome in humans is caused by the :
fertilization of an XX egg by a normal Y-bearing sperm
loss of half of the short arm of chromosome 5
loss of half of the long arm of chromosome 5
trisomy of 21st chromosome.
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