Embibe Experts Solutions for Chapter: Principles of Inheritance and Variation, Exercise 1: KCET (UG) 2021

Author:Embibe Experts

Embibe Experts Biology Solutions for Exercise - Embibe Experts Solutions for Chapter: Principles of Inheritance and Variation, Exercise 1: KCET (UG) 2021

Attempt the practice questions on Chapter 25: Principles of Inheritance and Variation, Exercise 1: KCET (UG) 2021 with hints and solutions to strengthen your understanding. EMBIBE CHAPTER WISE PREVIOUS YEAR PAPERS FOR BIOLOGY solutions are prepared by Experienced Embibe Experts.

Questions from Embibe Experts Solutions for Chapter: Principles of Inheritance and Variation, Exercise 1: KCET (UG) 2021 with Hints & Solutions

MEDIUM
KCET (UG)
IMPORTANT

The genotype of a husband and wife are IAIB & IAIO. Among the blood types of their children, how many different genotypes and phenotypes are possible?

MEDIUM
KCET (UG)
IMPORTANT

What is the possible blood group of children whose parents are heterozygous for A and B blood groups?

MEDIUM
KCET (UG)
IMPORTANT

In Morgan's experiment with Drosophila, when a yellow bodied white-eyed female was crossed with brown bodied red-eyed male and their F1 Progeny were intercrossed. What was the percentage of recombinants in the F2 generation?

EASY
KCET (UG)
IMPORTANT

From the chromosomal complements given below, identify the one which shows female heterogamety.

EASY
KCET (UG)
IMPORTANT

Sickle-cell anaemia is due to the following mutant gene :

EASY
KCET (UG)
IMPORTANT

In the following symbols, used in human pedigree analysis, identify the symbol that denotes consanguineous mating.

MEDIUM
KCET (UG)
IMPORTANT

Match the Column I with Column II and find the correct answer

  Column - I   Column - II
1 Aneuploidy p Increase in the whole set of chromosomes
2 Monoploidy q Loss or gain of a chromosome
3 Polyploidy r Two sets of chromosome
4 Diploidy s A single set of chromosomes

MEDIUM
KCET (UG)
IMPORTANT

Match the Column- I with Column - II

  Column - I   Column - II
i Autosomal trisomy p Turner's Syndrome
ii Allosomal trisomy q Mendelian disorder
iii Allosomal Monosomy r Klinefelter's Syndrome
iv Cystic fibrosis s Down's Syndrome