Which of the following is not a hereditary disease?

1. Haemophilia. 

2. Cretinism. 

3. Cystic fibrosis. 

4. Thalassemia.

Subtopic:  Mendelian Disorders |
 83%
From NCERT
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A person with Down syndrome will show all the given
symptoms except

1. Many loops on finger tips.
2. Flat back of head
3. Big and wrinkled tongue
4. Narrow round face

Subtopic:  Non - Disjunction & Aneuploidy |
 58%
From NCERT
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Two phenotypically normal individuals have an affected child. What can we conclude about the parents?

1. they both carried the diesease allele

2. they are not the parents of the child

3. they are affected

4. no conclusions can be drawn

Subtopic:  Mendelian Disorders |
 91%
From NCERT
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In a marriage between a male with blood group A and a female with blood group B, the progeny had either blood group AB or B. What could be the possible genotype of the parents?

1. IA i (Male) ; IB IB (Female)

2. IA IA (Male) ; IB IB (Female)

3. IA IA (Male) ; IB i (Female)

4. IA i (Male) ; IB i(Female)

Subtopic:  Dominance Deviation from Mendel: 2 |
 75%
From NCERT
NEET - 2019
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Match the items of Column - I with Column - II :

Column-I

Column-II
(a) XX-XO method of sex determination (i) Turner's syndrome
(b) XX-XY method of sex Determination (ii) Female heterogametic
(c) Karyotype-45 (iii) Grasshopper
(d) ZW-ZZ method of Sex Determination (iv) Female homogametic


Select the correct option from the following:

(a) (b) (c) (d)
1. (ii) (iv) (i) (iii)
2. (i) (iv) (ii) (iii)
3. (iii) (iv) (i) (ii)
4. (iv) (ii) (i) (iii)
Subtopic:  Sex Determination | Sex Aneuploidy - Turner & Klinefelter Syndrome |
 80%
From NCERT
NEET - 2019
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A normal woman, whose father had colour blindness, married a normal man. What is the chance of occurrence of colour blindness in the progeny?

1. 25%

2. 50%

3. 100%

4. 74%

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 72%
From NCERT
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Cystic fibrosis, Myotonic dystrophy and Thalassemia are

1. Chromosomal disorders

2. Autosomal recessive disorders

3. Mendelian disorders

4. Autosomal dominant disorders

Subtopic:  Mendelian Disorders |
 62%
From NCERT
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All are the characteristics of an individual from trisomy
of chromosome 21, except

1. Short stature

2. Gynaecomastia

3. Palm crease

4. Furrowed tongue

Subtopic:  Non - Disjunction & Aneuploidy |
 91%
From NCERT
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An individual with AaBb genotype is producing four types of gametes as AB, aB, Ab and ab by meiosis. If the frequency of these gametes is 25% each then, it explains

1.  Incomplete linkage

2.  Mutations

3.  Independent assortment 

4.  Complete linkage 

Subtopic:  Dihybrid Cross: Details |
 86%
From NCERT
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Which one of the following Mendelian trait controlling unit is expressed in homozygous condition only?

1.  Axial flower

2.  Yellow seed

3.  Yellow pod

4.  Smooth seed 

Subtopic:  Monohybrid Cross: 1 |
 77%
From NCERT
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