The F1 progeny in monohybrid crosses by Mendel resembled:

1. The parent exhibiting dominant trait completely

2. The parent exhibiting recessive trait completely

3. The parent exhibiting dominant trait partly

4. The parent exhibiting recessive trait partly

Subtopic:  Monohybrid Cross: 1 |
 82%
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Genes which code for a pair of contrasting traits or slightly different forms of the same gene are known as:

1.Alleles
2. Loci
3. Cistrons
4. Introns

Subtopic:  Monohybrid Cross: 1 |
 95%
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What is the ratio of a typical monohybrid test cross?

(1) 2 : 1

(2) 3 : 1

(3) 1: 2 : 1                

(4) 1 : 1

Subtopic:  Monohybrid Cross: 1 |
 64%
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When Mendel self hybridized F1 progeny of a dihybrid cross between pure Yellow Round seeded plants and Green Wrinkled plants, he observed that yellow and green colour segregated in a ratio of:

(1) 1 : 1

(2) 3 : 1

(3) 9 : 3 : 3 : 1

(4) 1 : 2 : 1

Subtopic:  Dihybrid Cross: Details |
 50%
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In 1900 Mendel’s work was rediscovered by:

1. Korana, Nirenberg and Mathei

2. De Vries, Correns and von Tschermak

3. Avery, McCleod and McCarty

4. Watson, Crick and Wilkins

Subtopic:  Monohybrid Cross: 1 |
 91%
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In humans, the mechanism of sex determination is:

(1) XX – XY; male heterogamety

(2) XX – XY; female heterogamety

(3) XX – XO; male heterogamety

(4) XX – XO; female heterogamety

Subtopic:  Sex Determination |
 93%
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A couple has a daughter. What is the probability that their next child will be a daughter?

(1) 0 %

(2) 25 %

(3) 50 %

(4) 100 %

Subtopic:  Sex Determination |
 92%
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Thalesemia is inherited as a/an ____________ condition.

(1) Autosomal recessive

(2) Autosomal dominant

(3) Sex linked recessive

(4) Sexlinked dominant

Subtopic:  Mendelian Disorders: Thalassemia |
 86%
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The point mutation in sickle cell anaemia leads to a change in codon. Identify the correct change:

(1) UGA to UAA

(2) GUG to GAG

(3) GAG to GUG

(4) UAA to UGA

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 82%
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In sickle cell anaemia, the mutant haemoglobin molecule undergoes

(1) Polymerisation under low oxygen tension causing that changes the shape of the RBC to sickle like structure

(2) Depolymerisation under low oxygen tension causing that changes the shape of the RBC to sickle like structure

(3) Denaturation under high oxygen tension causing that changes the shape of the RBC to sickle like structure

(4) Denaturation

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 79%
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