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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

If a genetic disease is transferred from a phenotypically normal but carrier female to only some of the male progeny, the disease is ______.

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प्रश्न

If a genetic disease is transferred from a phenotypically normal but carrier female to only some of the male progeny, the disease is ______.

विकल्प

  • Sex-linked recessive

  • Autosomal dominant

  • Sex-linked dominant

  • Autosomal recessive

MCQ
रिक्त स्थान भरें
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उत्तर

If a genetic disease is transferred from a phenotypically normal but carrier female to only some of the male progeny, the disease is sex-linked recessive.

Explanation:

If a genetic disease is passed from a phenotypically normal but carrier female to only some of the male offspring, it indicates a sex-linked recessive inheritance. In such cases, females can be carriers without showing symptoms because they have two X chromosomes, and the defective gene is recessive. Males, having only one X chromosome, exhibit the disease if they inherit the affected X from the carrier mother, leading to the disease manifesting only in some of the male progeny. This pattern is typical for diseases like haemophilia and color blindness.

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  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 5: Principle of Inheritance and Variation - MULTIPLE CHOICE QUESTIONS [पृष्ठ २९]

APPEARS IN

एनसीईआरटी एक्झांप्लर Biology Exemplar [English] Class 12
अध्याय 5 Principle of Inheritance and Variation
MULTIPLE CHOICE QUESTIONS | Q 4. | पृष्ठ २९
नूतन Biology [English] Class 12 ISC
अध्याय 4 Principles of Inheritance and Variation
Test Your Progress | Q 1. 94. | पृष्ठ २००

संबंधित प्रश्न

If only one 'X' chromosome is found in a female person, which of the following symptoms she will show?

  1. epicanthal skin fold
  2. webbing of neck
  3. small testis and absence of spermatogenesis
  4. presence of simian crease on the palm

Why is pedigree analysis done in the study of human genetics? State the conclusions that can be drawn from it.


Very Short Answer Question.

Give an example of a chromosomal disorder caused due to nondisjunction of autosomes.


In human beings 45 chromosomes/single X/XO abnormality causes ______.


A male rabbit of genotype 'AABBDDEE' is crossed with a female rabbit of genotype 'aabbddee' to produce F1 hybrid offspring. How many genetically different gametes can be produced by this F1 hybrid?


Identify the option that correctly represents the number of chromosomes in Down syndrome.


Rajesh and Mahesh have defective haemoglobin due to genetic disorders. Rajesh has too few globin molecules while Mahesh has incorrectly functioning globin molecules. Identify the disorder they are suffering from.

  Rajesh Mahesh
A. Sickle cell anaemia - an autosome linked recessive trait Thalassemia - an autosome linked dominant trait
B. Thalassemia - an autosome linked recessive blood disorder Sickle cell anaemia - an autosome linked recessive trait
C. Sickle cell anemia - an autosome linked recessive trait Thalassemia - an autosome linked recessive blood disorder
D. Thalassemia - an autosome linked recessive blood disorder Sickle cell anaemia - an autosome linked dominant trait

Why is the frequency of red-green colour blindness is many times higher in males than that in females?


Give definition of non-disjunction.


Which of the following correctly describes the composition of chromosomes in a normal human cell?


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