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
Give any 'two' names of X-linked diseases
What will be the phenotype of progeny, if a carrier haemophilic female marries a normal male?
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?
What is ‘syndrome’?
About 8% of the human male population suffers from colour blindness, whereas only about 0.4% of the human female population suffers from this disease. Write an explanation to show how it is possible.
Feminised males have ______ chromosomes.
If both parents are carriers for thalassaemia, which is an autosomal recessive disorder, what are the chances of pregnancy resulting in an affected child?
Failure of segregation of chromatids during cell division results in the gain or loss of chromosomes, this is called as ______.
“Genes contain the information that is required to express a particular trait.” Explain.
Describe Turner's syndrome.
