Advertisements
Advertisements
प्रश्न
Give the genotype of Klinefelter’s syndrome.
Advertisements
उत्तर
Klinefelter’s syndrome: 44 + XXY.
APPEARS IN
संबंधित प्रश्न
A colour-blind child is born to a normal couple. Work out a cross to show how it is possible. Mention the sex of this child.
Name the disorder caused by under secretion of thyroxine in children
Name a disorder a human suffers from as a result of the monosomy of the sex chromosome. Give the karyotype and write the symptoms.
Give a detail account of thalassemia.
If a genetic disease is transferred from a phenotypically normal but carrier female to only some of the male progeny, the disease is ______.
A disease caused by an autosomal primary non-disjunction is ______.
It is well known that Queen Victoria of England was a carrier for haemophilia. Since this is an X-linked disease, it can be predicted that ______.
Select the disease which is caused by recessive autosomal genes when present in homozygous conditions.
Clotting of blood is to ______.
Jacob is genetically a carrier of the disorder that affects the shape of the RBCs, as shown in the diagram below. His son James suffers from the same disorder.
- Give the biochemical reason for the disorder that changes the shape of the RBCs, as shown above.
- Draw a Punnett square to show the genotype of the mother of James.
- Name and define the type of 'point mutation' responsible for this disorder.
