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

(1) Tightly linked genes on the same chromosome show higher recombinations

(2) Genes far apart on the same chromosome show very few recombinations

(3) Genes loosely linked on the same chromosome show similar recombinations as the tightly linked ones

(4) Tightly linked genes on the same chromosome show very few recombinations.

Subtopic:  Linkage |
 79%
From NCERT
NEET - 2010
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh
Hints
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh

Which one of the following symbols and its representation, used in human pedigree analysis is correct?

(1) = Marriage between relatives

(2) = Unaffected male

(3) = Unaffected female

(4) = Male affected

Subtopic:  Pedigree Analysis: Basics |
 83%
From NCERT
NEET - 2010
Please attempt this question first.
Hints
Please attempt this question first.

Sickel cell anaemia is

(1) an autosomal linked dominant trait 

(2) caused by substitution of valine by glutamic acid in the β-globin chain of haemoglobin.

(3) caused by a change in base pair of DNA

(4) characterized by elongated sickle like RBCs with a nucleus. 

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
From NCERT
NEET - 2009
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh
Hints
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh

Point mutation involves

(1) insertion

(2) change in single base pair

(3) duplication

(4) deletion

Subtopic:  Mutation |
 90%
From NCERT
NEET - 2009
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh
Hints
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh

Study the pedigree chart given below

What does it show?

1. Inheritance of a sex-linked inborn error of metabolism like phenylketonuria
2. Inheritance of a condition like phenylketonuria as an autosomal recessive trait
3. The pedigree chart is wrong as this is not possible
4. Inheritance of a recessive sex-linked disease like haemophilia
Subtopic:  Pedigree Analysis: Problem Solving |
 70%
NEET - 2009
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh
Hints

Select the incorrect statement from the following

(1) linkage is an exception to the principle of independent assortment in heredity

(2) galactosemia is an inborn error of metabolism

(3) small population size results in random genetic drift in a population

(4) baldness is a sex limited trait

Subtopic:  Conclusion |
 56%
NEET - 2009
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh
Hints

Which one of the following condition in human is correctly matched with its chromosomal abnormality/linkage?

(1) Klinefelter's syndrome—44 autosomes + XXY

(2) Colourblindness —Y-linked

(3) Erythroblastosis foetalis— X-linked

(4) Down syndrome—44 autosomes + XO

 

Subtopic:  Non - Disjunction & Aneuploidy |
 79%
From NCERT
NEET - 2008
Please attempt this question first.
Hints
Please attempt this question first.

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 ?

(1) AaBb

(2) AaBB

(3) AABb

(4) AABB

Subtopic:  Dihybrid Cross Analysis |
 85%
NEET - 2007
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh
Hints

In the hexaploid wheat, the haploid (n) and basic (x) numbers of chromosomes are:

1. n = 7 and x = 21

2. n = 21 and x = 21

3. n = 21 and x = 14

4. n = 21 and x = 7

Subtopic:  Non - Disjunction & Aneuploidy |
NEET - 2007
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh
Hints

Inheritance of skin colour in humans is an example of :

(1) chromosomal aberration

(2) point mutation

(3) polygenic inheritance 

(4) codominance

Subtopic:  Polygenic Inheritance & Pleiotropy |
 90%
From NCERT
NEET - 2007
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh
Hints
To view explanation, please take trial in the course.
NEET 2021 - Achiever Batch - Aryan Raj Singh