- 1(current)
Q. No.What is the mode of inheritance of phenylketonuria?
| 1. | Autosomal recessive | 2. | Autosomal dominant |
| 3. | Sex linked recessive | 4. | Sex linked dominant |
Subtopic: Â Mendelian Disorders |
 88%
From NCERT
To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.
Hints
To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.
In Phenylketonuria,
| I. | Phenylpyruvic acid and other derivatives are accumulated in the brain resulting in mental retardation. |
| II. | These are also excreted through urine because of their poor absorption by the kidney. |
| 1. | Only I is correct | 2. | Only II is correct |
| 3. | Both are correct | 4. | Both are incorrect |
Subtopic: Â Mendelian Disorders |
 86%
From NCERT
To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.
Hints
To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.
Mendelian disorders are mainly determined by:
| 1. | Alteration or mutation in a single gene. |
| 2. | Chromosomal gross structural changes. |
| 3. | Recombination between linked genes. |
| 4. | Jumping genes |
Subtopic: Â Mendelian Disorders |
 82%
From NCERT
To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.
Hints
To unlock all the explanations of 38 chapters you need to be enrolled in MasterClass Course.
- 1(current)
Q. No.
© 2024 GoodEd Technologies Pvt. Ltd.