Multiple alleles control inheritance of (a) phenylketonuria (b) colour blindness (c) sickle cell anaemia (d) blood groups.

Multiple alleles control inheritance of
(a) phenylketonuria (b) colour blindness
(c) sickle cell anaemia (d) blood groups.
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1 Answer

Answer :

(d) blood groups.
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Related questions

In human beings, multiple genes are involved in the inheritance of (a) sickle-cell anaemia (b) skin colour (c) colour blindness (d) phenylketonuria.

Description : In human beings, multiple genes are involved in the inheritance of (a) sickle-cell anaemia (b) skin colour (c) colour blindness (d) phenylketonuria.

Last Answer : ) skin colour

A polygenic inheritance in human beings is (a) skin colour (b) phenylketonuria (c) colour blindness (d) sickle cell anaemia

Description : A polygenic inheritance in human beings is (a) skin colour (b) phenylketonuria (c) colour blindness (d) sickle cell anaemia

Last Answer : (a) skin colour

.Represented here is the inheritance pattern of a certain type of trait in humans. Which one of the following conditions could be an example of this pattern? (a) Phenylketonuria (b) Sickle cell anaemia (c) Haemophilia (d) Thalassemia

Description : .Represented here is the inheritance pattern of a certain type of trait in humans. Which one of the following conditions could be an example of this pattern? (a) Phenylketonuria (b) Sickle cell anaemia (c) Haemophilia (d) Thalassemia

Last Answer : (c) Haemophilia

Which of the following is an example of pleiotropy? (a) Haemophilia (b) Thalassemia (c) Sickle cell anaemia (d) Colour blindness

Description : Which of the following is an example of pleiotropy? (a) Haemophilia (b) Thalassemia (c) Sickle cell anaemia (d) Colour blindness

Last Answer : (c) Sickle cell anaemia

Pick out the correct statements. (1) Haemophilia is a sex-linked recessive disease. (2) Down’s syndrome is due to aneuploidy. (3) Phenylketonuria is an autosomal recessive gene disorder. (4) Sickle cell anaemia is an X-linked recessive gene disorder. (a) (1), (3) and (4) are correct. (b) (1), (2) and (3) are correct. (c) (1) and (4) are correct. (d) (2) and (4) are correct.

Description : Pick out the correct statements. (1) Haemophilia is a sex-linked recessive disease. (2) Down's syndrome is due to aneuploidy. (3) Phenylketonuria is an autosomal recessive gene disorder. (4) Sickle cell anaemia is an X- ... are correct. (c) (1) and (4) are correct. (d) (2) and (4) are correct.

Last Answer : (b) (1), (2) and (3) are correct.

Select the correct match. (a) Haemophilia – Y linked (b) Phenylketonuria – Autosomal dominant trait(c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11 (d) Thalassemia – X linked

Description : Select the correct match. (a) Haemophilia – Y linked (b) Phenylketonuria – Autosomal dominant trait (c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11 (d) Thalassemia – X linked

Last Answer : (c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11

The most striking example of point mutation is found in a disease called (a) Down’s syndrome (b) sickle cell anaemia (c) thalassaemia (d) night blindness.

Description : The most striking example of point mutation is found in a disease called (a) Down’s syndrome (b) sickle cell anaemia (c) thalassaemia (d) night blindness.

Last Answer : (b) sickle cell anaemia

Blood cancer is commonly known as – (1) Leucoderma (2) Leukaemia (3) Haemophilia (4) Sickle-cell. anaemia

Description : Blood cancer is commonly known as – (1) Leucoderma (2) Leukaemia (3) Haemophilia (4) Sickle-cell. anaemia

Last Answer : (2) Leukaemia Explanation: Leukemia is a cancer of blood and bone marrow. When a person has leukemia, the body makes too many white blood cells (leukocytes). The causes of most types of leukemia are not known. In general, all cancers have a breakdown in the normal way cell division is controlled.

A cross of a red cow (RR) with a white bull (WW) produces all roan offspring (RRWW). This type of inheritance is known as a. incomplete dominance. b. polygenic inheritance. c. codominance. d. multiple alleles.

Description : A cross of a red cow (RR) with a white bull (WW) produces all roan offspring (RRWW). This type of inheritance is known as a. incomplete dominance. b. polygenic inheritance. c. codominance. d. multiple alleles.

Last Answer : c. codominance.

Situations in which one allele for a gene is not completely dominant over another allele for that gene are called a. multiple alleles. b. incomplete dominance. c. polygenic inheritance. d. multiple genes.

Description : Situations in which one allele for a gene is not completely dominant over another allele for that gene are called a. multiple alleles. b. incomplete dominance. c. polygenic inheritance. d. multiple genes.

Last Answer : b. incomplete dominance.

Which one is a hereditary disease? (a) Cataract (b) Leprosy (c) Blindness (d) Phenylketonuria

Description : Which one is a hereditary disease? (a) Cataract (b) Leprosy (c) Blindness (d) Phenylketonuria

Last Answer : (d) Phenylketonuria

Haemoglobin SC disease: a. is common amongst Afro-carribean people b. does not show sickle cells in the blood film. c. causes severe anaemia d. causes retinal vein occlusion

Description : Haemoglobin SC disease: a. is common amongst Afro-carribean people b. does not show sickle cells in the blood film. c. causes severe anaemia d. causes retinal vein occlusion

Last Answer : causes retinal vein occlusion

Abnormal chain of amino acids in sickle cell anaemia is (A) Alpha chain (B) Beta chain (C) Delta chain (D) Gama chain

Description : Abnormal chain of amino acids in sickle cell anaemia is (A) Alpha chain (B) Beta chain (C) Delta chain (D) Gama chain

Last Answer : Answer : B

The oxygen dissociation curve is shifted to the right with: a. polycythaemia b. pyrexia c. respiratory acidosis d. sickle cell anaemia

Description : The oxygen dissociation curve is shifted to the right with: a. polycythaemia b. pyrexia c. respiratory acidosis d. sickle cell anaemia

Last Answer : pyrexia

Sickle cell anaemia induce to (a) change of amino acid in a-chain of haemoglobin (b) change of amino acid in b-chain of haemoglobin (c) change of amino acid in both a and b chains of haemoglobin (d) change of amino acid either a or b chains of haemoglobin.

Description : Sickle cell anaemia induce to (a) change of amino acid in a-chain of haemoglobin (b) change of amino acid in b-chain of haemoglobin (c) change of amino acid in both a and b chains of haemoglobin (d) change of amino acid either a or b chains of haemoglobin.

Last Answer : (b) change of amino acid in b-chain of haemoglobin

Which of the following is a correct match? (a) Down’s syndrome - 21st chromosome (b) Sickle cell anaemia - X-chromosome (c) Haemophilia - Y-chromosome (d) Parkinson’s disease - X and Y chromosome

Description : Which of the following is a correct match? (a) Down’s syndrome - 21st chromosome (b) Sickle cell anaemia - X-chromosome (c) Haemophilia - Y-chromosome (d) Parkinson’s disease - X and Y chromosome

Last Answer : a) Down’s syndrome - 21st chromosome

.Which one of the following conditions though harmful in itself, is also potential saviour from a mosquito borne infectious disease ? (a) Thalassaemia (b) Sickle cell anaemia (c) Pernicious anaemia (d) Leukaemia

Description : .Which one of the following conditions though harmful in itself, is also potential saviour from a mosquito borne infectious disease ? (a) Thalassaemia (b) Sickle cell anaemia (c) Pernicious anaemia (d) Leukaemia

Last Answer : (b) Sickle cell anaemia

Sickle cell anaemia has not been eliminated from the African population because (a) it is controlled by dominant genes (b) it is controlled by recessive genes (c) it is not a fatal disease (d) it provides immunity against malaria

Description : Sickle cell anaemia has not been eliminated from the African population because (a) it is controlled by dominant genes (b) it is controlled by recessive genes (c) it is not a fatal disease (d) it provides immunity against malaria

Last Answer : (d) it provides immunity against malaria.

Both sickle cell anaemia and Huntington’s chorea are (a) virus-related diseases (b) bacteria-related diseases (c) congenital disorders (d) pollutant-induced disorders.

Description : Both sickle cell anaemia and Huntington’s chorea are (a) virus-related diseases (b) bacteria-related diseases (c) congenital disorders (d) pollutant-induced disorders.

Last Answer : c) congenital disorders

. Sickle-cell anaemia is (a) caused by substitution of valine by glutamic acid in the beta globin chain of haemoglobin (b) caused by a change in a single base pair of DNA (c) characterized by elongated sickle like RBCs with a nucleus (d) an autosomal linked dominant trait.

Description : . Sickle-cell anaemia is (a) caused by substitution of valine by glutamic acid in the beta globin chain of haemoglobin (b) caused by a change in a single base pair of DNA (c) characterized by elongated sickle like RBCs with a nucleus (d) an autosomal linked dominant trait.

Last Answer : (b) caused by a change in a single base pair of DNA

.A disease caused by an autosomal primary non- disjunction is (a) Klinefelter’s syndrome (b) Turner’s syndrome (c) Sickle cell anaemia (d) Down’s syndrome.

Description : .A disease caused by an autosomal primary non- disjunction is (a) Klinefelter’s syndrome (b) Turner’s syndrome (c) Sickle cell anaemia (d) Down’s syndrome.

Last Answer : (d) Down’s syndrome.

Thalassemia and sickle cell anaemia are caused due to a problem in globin molecule synthesis. Select the correct statement. (a) Both are due to a quantitative defect in globin chain synthesis. (b) Thalassemia is due to less synthesis of globin molecules. (c) Sickle cell anaemia is due to a quantitative problem of globin molecules. (d) Both are due to a qualitative defect in globin chain synthesis.

Description : Thalassemia and sickle cell anaemia are caused due to a problem in globin molecule synthesis. Select the correct statement. (a) Both are due to a quantitative defect in globin chain synthesis. (b ... problem of globin molecules. (d) Both are due to a qualitative defect in globin chain synthesis.

Last Answer : (b) Thalassemia is due to less synthesis of globin molecules

Which one of the following statements is correct regarding sexually transmitted diseases (STDs)? (a) A person may contract syphilis by sharing milk with one already suffering from the disease. (b) Haemophilia is one of the STDs.(c) Genital herpes and sickle-cell anaemia are both STDs. (d) The chances of a 5-years boy contracting a STD are very little.

Description : Which one of the following statements is correct regarding sexually transmitted diseases (STDs)? (a) A person may contract syphilis by sharing milk with one already suffering from the disease. (b) Haemophilia is ... both STDs. (d) The chances of a 5-years boy contracting a STD are very little.

Last Answer : (d) The chances of a 5-years boy contracting a STD are very little.

Consider the following human diseases: 1. Anaemia 2. Haemophilia 3. Leukemia 4. Phenylketonuria Which of the above diseases are hereditary in nature? (a) 1, 2 and 3 (b) 1 and 4 (c) 2 and 3 (d) 2 and 4

Description : Consider the following human diseases: 1. Anaemia 2. Haemophilia 3. Leukemia 4. Phenylketonuria Which of the above diseases are hereditary in nature? (a) 1, 2 and 3 (b) 1 and 4 (c) 2 and 3 (d) 2 and 4

Last Answer : Ans:(d)

How is analyzing the inheritance patterns of sickle cell disease through pedigrees allowed scientists to determine that the disease is autosomal recessive?

Description : How is analyzing the inheritance patterns of sickle cell disease through pedigrees allowed scientists to determine that the disease is autosomal recessive?

Last Answer : Feel Free to Answer

Study the pedigree chart given below. What does it show? (a) Inheritance of a condition like phenylketonuria as an autosomal recessive trait. (b) The pedigree chart is wrong as this is not possible. (c) Inheritance of a recessive sex-linked disease like haemophilia. (d) Inheritance of a sex-linked inborn error of metabolism like phenylketonuria

Description : Study the pedigree chart given below. What does it show? (a) Inheritance of a condition like phenylketonuria as an autosomal recessive trait. (b) The pedigree chart is wrong as this is ... disease like haemophilia. (d) Inheritance of a sex-linked inborn error of metabolism like phenylketonuria

Last Answer : (a) Inheritance of a condition like phenylketonuria as an autosomal recessive trait.

Which of the following characteristics represent ‘inheritance of blood groups’ in humans? (i) Dominance (ii) Co-dominance (iii)Multiple allele (iv) Incomplete dominance (v) Polygenic inheritance (a) (ii), (iii) and (v) (b) (i), (ii) and (iii) (c) (ii), (iv) and (v) (d) (i), (iii) and (v)

Description : Which of the following characteristics represent ‘inheritance of blood groups’ in humans? (i) Dominance (ii) Co-dominance (iii)Multiple allele (iv) Incomplete dominance (v) Polygenic inheritance (a) (ii), (iii) and (v) (b) (i), (ii) and (iii) (c) (ii), (iv) and (v) (d) (i), (iii) and (v)

Last Answer : (b) (i), (ii) and (iii)

Which of the following characteristics represent 'Inheritance of blood groups' in humans ? a. Dominance b. Co-dominance c. Multiple dominance d. Incomplete dominance e. Polygenic inheritance (1) b, c and e (2) a, b and c (3) b, d and e (4) a, c and e

Description : Which of the following characteristics represent 'Inheritance of blood groups' in humans ? a. Dominance b. Co-dominance c. Multiple dominance d. Incomplete dominance e. Polygenic inheritance (1) b, c and e (2) a, b and c (3) b, d and e (4) a, c and e

Last Answer : (2) a, b and c

Abnormal chain of amino acids in sickle cells anaemia is (A) Alpha chain (B) Beta chain (C) Gama chain (D) Delta chain

Description : Abnormal chain of amino acids in sickle cells anaemia is (A) Alpha chain (B) Beta chain (C) Gama chain (D) Delta chain

Last Answer : Answer : B

$ Sicke cell anaemia is a type of pleiotropy. ! Sex linked inharitance is also called criss cross inheritance.

Description : $ Sicke cell anaemia is a type of pleiotropy. ! Sex linked inharitance is also called criss cross inheritance.

Last Answer : $ Sicke cell anaemia is a type of pleiotropy. ! Sex linked inharitance is also called criss cross inheritance ... wrong D. If both As and R are wrong.

The deficiency of iron in man result in (1) Anaemia (2) Night, blindness (3) Scurvy (4) Rickets

Description : The deficiency of iron in man result in (1) Anaemia (2) Night, blindness (3) Scurvy (4) Rickets

Last Answer : (1) Anaemia Explanation: Anaemia is a condition in which the number of red blood cells or their oxygencarrying capacity is insufficient to meet physiologic needs, which vary by age, sex, altitude, ... , and pregnancy status. Iron deficiency is thought to be the most common cause of anaemia globally

The deficiency of iron in man result in (1) Anaemia (2) Night blindness (3) Scurvy (4) Rickets

Description : The deficiency of iron in man result in (1) Anaemia (2) Night blindness (3) Scurvy (4) Rickets

Last Answer : Anaemia

What type of inheritance pattern (are the A and B alleles to each other (Autosomal dominant-Regular dominant-recessive relationship, X linked, co-dominant, incomplete dominant)?

Description : What type of inheritance pattern (are the A and B alleles to each other (Autosomal dominant-Regular dominant-recessive relationship, X linked, co-dominant, incomplete dominant)?

Last Answer : Incomplete dominance

.Match the terms in column I with their description in column II and choose the correct option. Column I Column II A. Dominance (i) Many genes govern a single character B. Co-dominance (ii) In a heterozygous organism only one allele expresses itself C. Pleiotropy (iii) In a heterozygous organism both alleles express themselves fully D. Polygenic (iv) A single gene inheritance influences many characters A B C D (a) (iv) (i) (ii) (iii) (b) (iv) (iii) (i) (ii) (c) (ii) (i) (iv) (iii) (d) (ii) (iii) (iv) (i)

Description : .Match the terms in column I with their description in column II and choose the correct option. Column I Column II A. Dominance (i) Many genes govern a single character B. Co-dominance (ii) In a heterozygous organism only one allele ... (i) (ii) (c) (ii) (i) (iv) (iii) (d) (ii) (iii) (iv) (i)

Last Answer : (d) (ii) (iii) (iv) (i)

ABO blood groups in humans are controlled by the gene I. It has three alleles - IA, IB and i. Since there are three different alleles, six different genotypes are possible. How many phenotypes can occur? (a) Three (b) One (c) Four (d) Two

Description : ABO blood groups in humans are controlled by the gene I. It has three alleles - IA, IB and i. Since there are three different alleles, six different genotypes are possible. How many phenotypes can occur? (a) Three (b) One (c) Four (d) Two

Last Answer : (c) Four

Identify the wrong statement with reference to the gene ‘I’ that controls ABO blood groups. (a) The gene (I) has three alleles. (b) A person will have only two of the three alleles. (c) When IA and IB are present together, they express same type of sugar. (d) Allele i does not produce any sugar.

Description : Identify the wrong statement with reference to the gene ‘I’ that controls ABO blood groups. (a) The gene (I) has three alleles. (b) A person will have only two of the three alleles. (c) When IA and IB are present together, they express same type of sugar. (d) Allele i does not produce any sugar.

Last Answer : (c) When IA and IB are present together, they express same type of sugar.

Which cell disorder in our body is responsible for colour blindness? (1) WBC (2) Cone cell (3) Red Cell (4) Neuron

Description : Which cell disorder in our body is responsible for colour blindness? (1) WBC (2) Cone cell (3) Red Cell (4) Neuron

Last Answer : (2) Cone cell Explanation: Colour vision deficiency, commonly called colour blindness, results from a malfunction or absence of cone cells in the retina. Cone cellsare one of three types of ... of the human eye that is responsible for colour vision and function best in relatively bright lights.

Which cell disorder in our body is responsible for colour blindness? (1) WBC (2) Cone cell (3) Red Cell (4) Neuron

Description : Which cell disorder in our body is responsible for colour blindness? (1) WBC (2) Cone cell (3) Red Cell (4) Neuron

Last Answer : Cone cell

Why is blood type an example of multiple alleles?

Description : Why is blood type an example of multiple alleles?

Last Answer : Multiple Alleles:The ABO blood group in humans is determined by multiple alleles of a single gene. There are four possible phenotypes for this character: A person's blood may be either A, B, ... adds neither A nor B. Because each person carries two alleles, six genotypes are possible, resulting in

Which of the following pairs is wrongly matched? (a) Starch synthesis in pea : Multiple alleles (b) ABO blood grouping : Co-dominance (c) XO type sex determination: Grasshopper (d) T.H. Morgan : Linkage

Description : Which of the following pairs is wrongly matched? (a) Starch synthesis in pea : Multiple alleles (b) ABO blood grouping : Co-dominance (c) XO type sex determination: Grasshopper (d) T.H. Morgan : Linkage

Last Answer : (a) Starch synthesis in pea : Multiple alleles

Which of the following pairs in wrongly matched ? (1) Starch synthesis in pea : Multiple alleles (2) ABO blood grouping : Co-dominance (3) XO type sex determination : Grasshopper (4) T.H. Morgan : Linkage

Description : Which of the following pairs in wrongly matched ? (1) Starch synthesis in pea : Multiple alleles (2) ABO blood grouping : Co-dominance (3) XO type sex determination : Grasshopper (4) T.H. Morgan : Linkage

Last Answer : (1) Starch synthesis in pea : Multiple alleles

ABO blood group system is due to (a) multifactor inheritance (b) incomplete dominance (c) multiple allelism (d) epistasis.

Description : ABO blood group system is due to (a) multifactor inheritance (b) incomplete dominance (c) multiple allelism (d) epistasis.

Last Answer : (c) multiple allelism

Is colour blindness a good thing?

Description : Is colour blindness a good thing?

Last Answer : My husband and my father are both color blind, and I always find myself frustrated with their inability to make out the same colors that I can. Trying to choose paint for the walls or any comparable task becomes ... eyes. However, if it works for you and you can see the positive, I say run with it.

$ `X X^(C)` represents the genotype of a human femanle which acts as carrier of genes for colour blindness. ! Any change in the structure of a chromos

Description : $ `X X^(C)` represents the genotype of a human femanle which acts as carrier of genes for colour blindness. ! Any change in the structure of a chromos

Last Answer : $ `X X^(C)` represents the genotype of a human femanle which acts as carrier of genes for colour blindness ... is wrong D. If both As and R are wrong.

Which of the following tests is used for the diagnosis of ‘Colour-Blindness’ in people?

Description : Which of the following tests is used for the diagnosis of ‘Colour-Blindness’ in people?

Last Answer : Ishihara Test

A man with colour blindness will see red as - (1) Yellow (2) Blue (3) Green (4) Violet

Description : A man with colour blindness will see red as - (1) Yellow (2) Blue (3) Green (4) Violet

Last Answer : (3) Green Explanation: Colour-blindness is the inability to distinguish the differences between certain colours. This condition results from an absence of colour-sensitive pigment in the cone cells of the ... type is red-green colour-blindness, where red and green are seen as the same color.

Colour blindness is more common in men than women.

Description : Colour blindness is more common in men than women.

Last Answer : Ans: Women have the sex chromosomes XX, while men have the chromosomes XY. The gene for normal colour vision is found on the X-chromosome. If a woman has one Xchromosome with the gene ... colour vision gene. This is less probable mathematically than having just one X-chromosome missing the gene.

Give scientific reason of the following : a) Colour blindness is more common in men than in women b) Light coloured clothes are generally worn in summer c) A person is hurt more when he falls on hard ground than on soft d) Deforestation causes more floods e) The man-hole covers are generally round

Description : Give scientific reason of the following : a) Colour blindness is more common in men than in women b) Light coloured clothes are generally worn in summer c) A person is hurt more when he falls ... ground than on soft d) Deforestation causes more floods e) The man-hole covers are generally round

Last Answer : a) Colour blindness is more common in men than in women Women have the sex chromosomes XX, while men have the chromosomes XY. The gene for normal colour vision is found on the X- ... of flowing water. When these trees are cut the natural barriers ultimately vanish and more floods are caused

The visual acuity is affected by: a. pupil size b. illumination of the target c. red-green colour blindness d. contrast

Description : The visual acuity is affected by: a. pupil size b. illumination of the target c. red-green colour blindness d. contrast

Last Answer : contrast

The colour blindness is more likely to occur in males than in females because (a) the Y-chromosome of males have the genes for distinguishing colours (b) genes for characters are located on the sex- chromosomes (c) the trait is dominant in males and recessive in females (d) none of these.

Description : The colour blindness is more likely to occur in males than in females because (a) the Y-chromosome of males have the genes for distinguishing colours (b) genes for characters are located on the sex- chromosomes (c) the trait is dominant in males and recessive in females (d) none of these.

Last Answer : (b) genes for characters are located on the sex- chromosomes