342441
Colour blindness occurs in about 8 per cent of males and only about 0.4 per cent of females. This statements explains that
1 Males have two X chromosome
2 Males have only one X chromosome
3 females have no X chromosome
4 females have only one X chromosome
Explanation:
This is because the genes that lead to redgreen colour blindness are on the X chromosome. Males have only one X chromosome and females have two.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342442
Statement A : Colour blindness is more common in males than in females. Statement B : In colourblindness a person cannot differentiate between red and green colours.
1 Statement A is correct but Statement B is incorrect.
2 Statement A is incorrect but Statement B is correct.
3 Both Statements are correct.
4 Both Statements are incorrect.
Explanation:
Both statements are correct.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342443
Gene for colourblindness is located on
1 Non-homologous part of Y-chromosome
2 Homologous part of X- chromosomes
3 Homologous part of Y- chromosome
4 Non- homologous part of X- chromosomes
Explanation:
Genes for colourblindness are located on the X chromosome, which is one of the two sex chromosomes and it is located on the non homologous part of the X- chromosome. Colourblindness is a sex linked recessive disease, it most often occurs in males.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342444
Match the columns I and II with respect to Colour blindness Column I Column II A Normal female P \({X^c}{X^c}\) B Carrier female Q \({X^C}{X^C}\) C Diseased female R \({X^C}{X^c}\) D Diseased male S \({X^c}{Y^c}\)
342441
Colour blindness occurs in about 8 per cent of males and only about 0.4 per cent of females. This statements explains that
1 Males have two X chromosome
2 Males have only one X chromosome
3 females have no X chromosome
4 females have only one X chromosome
Explanation:
This is because the genes that lead to redgreen colour blindness are on the X chromosome. Males have only one X chromosome and females have two.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342442
Statement A : Colour blindness is more common in males than in females. Statement B : In colourblindness a person cannot differentiate between red and green colours.
1 Statement A is correct but Statement B is incorrect.
2 Statement A is incorrect but Statement B is correct.
3 Both Statements are correct.
4 Both Statements are incorrect.
Explanation:
Both statements are correct.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342443
Gene for colourblindness is located on
1 Non-homologous part of Y-chromosome
2 Homologous part of X- chromosomes
3 Homologous part of Y- chromosome
4 Non- homologous part of X- chromosomes
Explanation:
Genes for colourblindness are located on the X chromosome, which is one of the two sex chromosomes and it is located on the non homologous part of the X- chromosome. Colourblindness is a sex linked recessive disease, it most often occurs in males.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342444
Match the columns I and II with respect to Colour blindness Column I Column II A Normal female P \({X^c}{X^c}\) B Carrier female Q \({X^C}{X^C}\) C Diseased female R \({X^C}{X^c}\) D Diseased male S \({X^c}{Y^c}\)
342441
Colour blindness occurs in about 8 per cent of males and only about 0.4 per cent of females. This statements explains that
1 Males have two X chromosome
2 Males have only one X chromosome
3 females have no X chromosome
4 females have only one X chromosome
Explanation:
This is because the genes that lead to redgreen colour blindness are on the X chromosome. Males have only one X chromosome and females have two.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342442
Statement A : Colour blindness is more common in males than in females. Statement B : In colourblindness a person cannot differentiate between red and green colours.
1 Statement A is correct but Statement B is incorrect.
2 Statement A is incorrect but Statement B is correct.
3 Both Statements are correct.
4 Both Statements are incorrect.
Explanation:
Both statements are correct.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342443
Gene for colourblindness is located on
1 Non-homologous part of Y-chromosome
2 Homologous part of X- chromosomes
3 Homologous part of Y- chromosome
4 Non- homologous part of X- chromosomes
Explanation:
Genes for colourblindness are located on the X chromosome, which is one of the two sex chromosomes and it is located on the non homologous part of the X- chromosome. Colourblindness is a sex linked recessive disease, it most often occurs in males.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342444
Match the columns I and II with respect to Colour blindness Column I Column II A Normal female P \({X^c}{X^c}\) B Carrier female Q \({X^C}{X^C}\) C Diseased female R \({X^C}{X^c}\) D Diseased male S \({X^c}{Y^c}\)
342441
Colour blindness occurs in about 8 per cent of males and only about 0.4 per cent of females. This statements explains that
1 Males have two X chromosome
2 Males have only one X chromosome
3 females have no X chromosome
4 females have only one X chromosome
Explanation:
This is because the genes that lead to redgreen colour blindness are on the X chromosome. Males have only one X chromosome and females have two.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342442
Statement A : Colour blindness is more common in males than in females. Statement B : In colourblindness a person cannot differentiate between red and green colours.
1 Statement A is correct but Statement B is incorrect.
2 Statement A is incorrect but Statement B is correct.
3 Both Statements are correct.
4 Both Statements are incorrect.
Explanation:
Both statements are correct.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342443
Gene for colourblindness is located on
1 Non-homologous part of Y-chromosome
2 Homologous part of X- chromosomes
3 Homologous part of Y- chromosome
4 Non- homologous part of X- chromosomes
Explanation:
Genes for colourblindness are located on the X chromosome, which is one of the two sex chromosomes and it is located on the non homologous part of the X- chromosome. Colourblindness is a sex linked recessive disease, it most often occurs in males.
BIOXII05: PRINCIPLES OF INHERITANCE AND VARIATION
342444
Match the columns I and II with respect to Colour blindness Column I Column II A Normal female P \({X^c}{X^c}\) B Carrier female Q \({X^C}{X^C}\) C Diseased female R \({X^C}{X^c}\) D Diseased male S \({X^c}{Y^c}\)