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What Will Be the Phenotype of Progeny, If a Carrier Haemophilic Female Marries a Normal Male? - Biology

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प्रश्न

What will be the phenotype of progeny, if a carrier haemophilic female marries a normal male?

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उत्तर

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2014-2015 (March)

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संबंधित प्रश्न

Give any 'two' names of X-linked diseases


Give an example of a human disorder that is caused due to a single gene mutation.


In which of the following disorders number of chromosomes present is 47?
(A) Turner’s syndrome
(B) Cushing’s syndrome
(C) Acquired Immuno - Deficiency Syndrome
(D) Down’s syndrome


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


Read the following and answer from given below:

Turner's syndrome is an example of monosomy. It is formed by the union of an allosome-free egg and a normal 'X' containing sperm or a normal egg and an allosome-free sperm. The individual has 2n = 45 chromosomes (44 + X0) instead of 46. Such individuals are sterile females who have rudimentary ovaries, underdeveloped breasts, small uterus, short stature, webbed neck, and abnormal intelligence. They may not menstruate or ovulate. This disorder can be treated by giving female sex hormones to women from the age of puberty to make them develop breasts and have menstruation. This makes them feel more normal.

Turner's syndrome is a/an ______ 


Which of the following is called as Royal disease?


“Genes contain the information that is required to express a particular trait.” Explain.


What is the genotype of Turner's Syndrome?


What are chromosomal disorders?


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.

  1. Give the biochemical reason for the disorder that changes the shape of the RBCs, as shown above.
  2. Draw a Punnett square to show the genotype of the mother of James.
  3. Name and define the type of 'point mutation' responsible for this disorder.

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