What phenotypic ratio will be there when selfing of a trihybrid is performed in which two gene pairs are completely dominant and one gene pair is codominant?

    1. 3:9:1:2:1:3
    2. 27:9:3:1:3:3:1
    3. 9:3:3:1:18:6:6:2:9:3:3:1
    4. 18:6:6:2:1:2:1:2:1

Subtopic:  Dihybrid Cross: General Consideration |
 62%
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If dihybrid mulatto male (AaBb) is crossed with white female(aabb), then the ratio of mulatto and white offspring will be-

    1. 1:6
    2. 1:1
    3. 4:1
    4. 2:1
Subtopic:  Dihybrid Cross: Details |
 72%
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In a test cross of F1 generation, having a genotype AaBb, following progeny were obtained

AaBb- 450

aabb – 450

Aabb- 50

aaBb- 50

How far in centimorgans are the a and b genes?

a.100

b.90

c.10

d.1

Subtopic:  Monohybrid Cross: Further Understanding |
 54%
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The distance between gene A, B, C and D on a chromosome is as follows:

A and C - 18 units

A and B - 26 units

A and D - 40 units

B and C - 8 units

B and D – 14 units

The sequence of these genes would be-

    1. ABCD
    2. ACBD
    3. ADCB
    4. ACDB
Subtopic:  Monohybrid Cross: Further Understanding |
 80%
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Which of the following is an autosomal recessive blood disease?

    1. Phenylketonuria
    2. Thalassemia
    3. Haemophilia
    4. Muscular dystrophy
Subtopic:  Mendelian Disorders |
 69%
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Which of the following are correct with respect to Thalassemia?

    1. An autosomal dominant disorder
    2. Defect due to mutation or deletion
    3. Parents will be homozygous for thalassemia
    4. Occurs due to vitamin deficiency
Subtopic:  Mendelian Disorders: Thalassemia |
 71%
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Read the following statements with respect to Thalassemia and find the wrong one.

    1. Quantitative disorder
    2. Different forms of Thalassemia are observed
    3. Anaemia is not a characteristic feature of this disease
    4. Defect due to mutation and deletion
Subtopic:  Mendelian Disorders: Thalassemia |
 79%
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How sickle cell anaemia is different from Thalassemia?

(1) Being autosomal recessive

(2) Being a blood disease

(3) Being a qualitative disorder

(4) Involvement of mutation

Subtopic:  Mendelian Disorders: Thalassemia |
 85%
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The basis of Thalassemia classification can be-

(1) Which parent is affected

(2) Which chain of haemoglobin molecule is affected

(3) How much a chain is affected

(4) Which gender is showing the disease

Subtopic:  Mendelian Disorders: Thalassemia |
 80%
From NCERT
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Alpha Thalassemia is controlled by ------- on chromosome number----

(1) Linked gene, 11

(2) Linked gene, 16

(3) Unlinked gene, 11

(4) Unlinked gene, 16

Subtopic:  Mendelian Disorders: Thalassemia |
 74%
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