Advertisements
Advertisements
प्रश्न
Give the genotype of Turner’s syndrome.
Advertisements
उत्तर
The genotype of Turner’s syndrome is represented by (44 + XO).
APPEARS IN
संबंधित प्रश्न
Given below is the representation of amino acid composition not the relevant translated portion of β-chain of haemoglobin, related to the shape of human red blood cells

(a) Is this representation indicating a normal human or a sufferer from certain related genetic disease? Give reason in support of your answer.
(b) What difference would be noticed in the phenotype of the normal and the sufferer related to this gene?
(c) Who are likely to suffer more from the defect related to the gene represented the males, the females or both males and females equally? And why?
Why is pedigree analysis done in the study of human genetics? State the conclusions that can be drawn from it.
Identify ‘a’, ‘b’, ‘c’, ‘d’, ‘e’ and ‘f’ in the table given below:
| S. No. | Syndrome | Cause | Characteristics of affected individuals | Sex (male/female/both) |
| 1. | Down’s | Trisomy of 21 |
‘a’ |
‘b’ |
| 2. | ‘c’ | XXY | Overall masculine development | ‘d’ |
| 3. | Turner’s | 45 with XO |
‘e’ |
‘f’ |
The genotype of a person withTumer's syndrome will be:
(i) 44+XXY
(ii) 44+XYY
(iii) 44+XO
(iv) 44+XXYY
Give an account of one Mendelian and one chromosomal disorder you have studied.
Feminised males have ______ chromosomes.
Following list indicates various genetic diseases. Identify the diseases that are not caused due to single gene defect.
Huntington's chorea, alkaptonuria, Sickle cell anaemia, Down syndrome, thalassemia, Taysachs disease, Turner syndrome, cystic fibrosis, haemophi Lia, Klinefelter syndrome, albinism
Mental retardation in man associated with sex chromosomal abnormality is usually due to ______.
If a father and son are both defective in red-green colour vision, is it likely that the son inherited the trait from his father? Comment.
Which of the folowing is a correct match?
