This Page Score: 0/40
Match List-I (Genetic Disorder) with List-II (Defining Feature):
| List-I | List-II |
|---|---|
| A. Haemophilia | I. X-linked recessive, single protein in clotting cascade affected |
| B. Colour blindness | II. Defect in red or green cone of eye, X-linked recessive |
| C. Sickle-cell anaemia | III. Autosomal recessive, polymerisation of mutant haemoglobin |
| D. Phenylketonuria | IV. Autosomal recessive, lack of enzyme converting phenylalanine to tyrosine |
[Principles-of-Inheritance-and-Variation] [class-xii ]
Match List-I (Monohybrid Genotype) with List-II (F2 Proportion):
| List-I (Genotype) | List-II (Proportion in F2) |
|---|---|
| A. TT (Homozygous Dominant) | I. 1/4 |
| B. Tt (Heterozygous) | II. 1/2 |
| C. tt (Homozygous Recessive) | III. 1/4 |
| D. Tt (Phenotype expressed) | IV. Tall |
[Principles-of-Inheritance-and-Variation] [class-xii ]
Match List-I (Haplodiploid Male Feature) with List-II (Consequence):
| List-I (Drone Feature) | List-II (Result) |
|---|---|
| A. Develops from unfertilised egg | I. Is haploid (16 chromosomes) |
| B. Produces sperm by Mitosis | II. Sperm are genetically identical to the male |
| C. Does not have a father | III. Cannot have sons |
| D. Has a grandfather | IV. Can have grandsons |
[Principles-of-Inheritance-and-Variation] [class-xii ]
Match List-I (Inheritance Type) with List-II (Phenotypic Trait/Condition):
| List-I | List-II |
|---|---|
| A. Single gene multiple effect | I. Pleiotropy (e.g., Phenylketonuria) |
| B. Multiple genes plus environment | II. Polygenic inheritance (e.g., Human height) |
| C. Intermediate phenotype in F1 | III. Incomplete Dominance (e.g., Pink Snapdragon) |
| D. F1 resembles both parents | IV. Co-dominance (e.g., AB blood type) |
[Principles-of-Inheritance-and-Variation] [class-xii ]
Match List-I (Chromosomal Disorder Symptom) with List-II (Affected Organ/System):
| List-I (Symptom/Feature) | List-II (Syndrome) |
|---|---|
| A. Mental retardation, partially open mouth | I. Down’s Syndrome (Trisomy 21) |
| B. Gynaecomastia | II. Klinefelter’s Syndrome (XXY) |
| C. Rudimentary ovaries | III. Turner’s Syndrome (X0) |
| D. Polyploidy (in plants) | IV. Increase in a whole set of chromosomes |
[Principles-of-Inheritance-and-Variation] [class-xii ]
Match List-I (Gamete Type) with List-II (Sex/Organism):
| List-I (Gamete types produced) | List-II (Sex/Mechanism) |
|---|---|
| A. X or Y chromosome carrying sperm | I. Male heterogamety (Humans/Drosophila) |
| B. X or no X carrying sperm | II. Male heterogamety (Grasshopper) |
| C. Z or W chromosome carrying ovum | III. Female heterogamety (Birds) |
| D. Only X carrying ovum | IV. Female homogamety (Humans/Drosophila) |
[Principles-of-Inheritance-and-Variation] [class-xii ]
Match List-I (Allele Relationship) with List-II (Description of Allele):
| List-I | List-II |
|---|---|
| A. Dominant Allele | I. Unmodified (functioning) allele that produces normal enzyme |
| B. Recessive Allele (typical) | II. Modified allele producing non-functional or no enzyme |
| C. Allele producing less efficient enzyme | III. May lead to an effected (recessive) phenotype |
| D. Allele producing equivalent enzyme | IV. Results in the same phenotype as the unmodified allele |
[Principles-of-Inheritance-and-Variation] [class-xii ]
Match List-I (Human Genetic Disorder) with List-II (Inheritance Pattern):
| List-I (Disorder) | List-II (Inheritance) |
|---|---|
| A. Haemophilia | I. X-linked recessive |
| B. Sickle-cell anaemia | II. Autosome linked recessive |
| C. Myotonic dystrophy | III. Autosomal dominant |
| D. Colour Blindness | IV. X-linked recessive |
[Principles-of-Inheritance-and-Variation] [class-xii ]
Assertion (A):
In a monohybrid cross between tall (TT) and dwarf (tt) pea plants, all the F1 progeny are tall.
Reason (R):
The Law of Dominance states that in a dissimilar pair of factors, one factor (T) dominates the other (t), and is expressed in the F1 generation.
[Principles-of-Inheritance-and-Variation] [class-xii ]
Assertion (A):
The recessive parental trait is expressed without any blending in the F2 generation of a monohybrid cross.
Reason (R):
The Law of Segregation is based on the fact that alleles do not show any blending and they separate from each other during gamete formation.
[Principles-of-Inheritance-and-Variation] [class-xii ]
This Page Score: 0/40