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प्रश्न
The genotype of a person withTumer's syndrome will be:
(i) 44+XXY
(ii) 44+XYY
(iii) 44+XO
(iv) 44+XXYY
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उत्तर
44 + XO
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संबंधित प्रश्न
Give the genotype of Turner’s syndrome.
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?
Name the disorder caused by under secretion of thyroxine in children
Match the Column-I with Column-II and choose the CORRECT answer
| Column-I | Column-II | ||
| P. | Klinefelter syndrome | i. | Mutation in autosomal gene |
| Q. | Thalassaemia | ii. | Mutation sex chromosome linked gene |
| R. | Down syndrome | iii. | Trisomy of autosome |
| S. | Colour blindness | iv. | Trisomy of sex chromosome |
Thalassemia and sickle cell anaemia are caused due to a problem in globin molecule synthesis. Identify the correct statement from the following.
Select the incorrect statement regarding pedigree analysis.
Failure of segregation of chromatids during cell division results in the gain or loss of chromosomes, this is called as ______.
Trisomy is represented by ______.
Why is the frequency of red-green colour blindness is many times higher in males than that in females?
What are chromosomal disorders?
