An abnormal human of the karyotype 49, XXXYY will form how many Barr bodies?

1. 1
2. 2
3. 3
4. 4

Subtopic:  Sex Determination: Further Considerations |
 73%
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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 |
 81%
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NEET - 2019
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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 |
 76%
From NCERT
NEET - 2019
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In which genetic condition, each cell in the affected person, has three sex chromosomes XXY?

1. Thalassemia

2. Klinefelter's Syndrome

3. Phenylketonuria

4. Turner's Syndrome

Subtopic:  Sex Aneuploidy - Turner & Klinefelter Syndrome |
 87%
From NCERT
NEET - 2019
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“Chromosomes, which are seen in all dividing cells and pass from one generation to the next, are the basis for all genetic inheritance”.
This statement is credited to:

 
1. Watson and Crick 2. Hershey and Chase
3. Sutton and Boveri 4. Meselson and Stahl

Subtopic:  Chromosomal Basis of Inheritance: Introduction |
 80%
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A disease caused by an autosomal primary non-disjunction is:
1. Down's Syndrome
2. Klinefelter's Syndrome
3. Turner's Syndrome
4. Sickle Cell Anemia

Subtopic:  Non - Disjunction & Aneuploidy |
 78%
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Thalassemia and sickle cell anemia are caused due to a problem in globin molecule synthesis. Select the correct statement :

1. Both are due to a qualitative defect in globin chain synthesis.
2. Both are due to a quantitative defect in globin chain synthesis.
3. Thalassemia is due to less synthesis of globin molecules.
4. Sickle cell anemia is due to a quantitative problem of globin molecules
Subtopic:  Mendelian Disorders: Sickle Cell Anemia | Mendelian Disorders: Thalassemia | Additional Note on Thalassemia |
 78%
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The genotypes of a Husband and Wife are IAIB and IAi .
Among the blood types of their children how many different genotypes and phenotypes are possible
1. 3 genotypes ; 3 phenotypes
2. 3 genotypes; 4 phenotypes
3. 4 genotypes ; 3 Phenotypes
4. 4 genotypes ; 4 phenotypes

Subtopic:  Monohybrid Cross: Further Understanding |
 79%
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The mechanism that causes a gene to move from one linkage group to another is called
1. Crossing-over
2. inversion
3. duplication
4. translocation

Subtopic:  Mutation |
 75%
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A cell at the telophase stage is observed by a student in a plant brought from the field. He tells his teacher that this cell is not like other cells at the telophase stage. There is no formation of the cell plate and thus the cell is containing more chromosomes as compared to other dividing cells. This would result in:
1. Polyteny
2. Aneuploidy
3. Polyploidy
4. Somaclonal variation

Subtopic:  Non - Disjunction & Aneuploidy |
 82%
From NCERT
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