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)?

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)?
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Incomplete dominance
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Which type of Mendelian inherited condition results in both genders being affected equally in a vertical pattern? a) Automosomal dominant inheritance An individual who has an autosomal dominant inherited condition carries a gene mutation for that condition on one chromosome of a pair. b) Automosomal recessive inheritance The pattern of inheritance in autosomal recessive inherited conditions is different from that of autosomal dominant inherited conditions in that it is more horizontal than vertical, with relatives of a single generation tending to have the condition. c) X-linked inheritance X-linked conditions may be inherited in families in recessive or dominant patterns.

Description : Which type of Mendelian inherited condition results in both genders being affected equally in a vertical pattern? a) Automosomal dominant inheritance An individual who has an autosomal dominant ... that combine during early embryonic development leading to incomplete closure of the neural tube.

Last Answer : a) Automosomal dominant inheritance An individual who has an autosomal dominant inherited condition carries a gene mutation for that condition on one chromosome of a pair.

Inheritance of primary gout is (A) Autosomal recessive (B) Autosomal dominant (C) X-linked recessive (D) X-linked dominant

Description : Inheritance of primary gout is (A) Autosomal recessive (B) Autosomal dominant (C) X-linked recessive (D) X-linked dominant

Last Answer : Answer : C

A man and a woman, who do not show any apparent signs of a certain inherited disease, have seven children (2 daughters and 5 sons). Three of the sons suffer from the given disease but none of the daughters affected. Which of the following mode of inheritance do you suggest for this disease? (a) Sex-linked dominant (b) Sex-linked recessive (c) Sex-limited recessive (d) Autosomal dominant

Description : A man and a woman, who do not show any apparent signs of a certain inherited disease, have seven children (2 daughters and 5 sons). Three of the sons suffer from the given disease but none ... ? (a) Sex-linked dominant (b) Sex-linked recessive (c) Sex-limited recessive (d) Autosomal dominant

Last Answer : (b) Sex-linked recessive

A gene showing co-dominance has (a) alleles that are recessive to each other (b) both alleles independently expressed in the heterozygote (c) one allele dominant on the other (d) alleles tightly linked on the same chromosome.

Description : A gene showing co-dominance has (a) alleles that are recessive to each other (b) both alleles independently expressed in the heterozygote (c) one allele dominant on the other (d) alleles tightly linked on the same chromosome.

Last Answer : (b) both alleles independently expressed in the heterozygote

n the following human pedigree, the filled symbols represent the affected individuals. Identify the type of given pedigree. (i) (ii) (iii) (iv) (a) Autosomal recessive (b) X-linked dominant (c) Autosomal dominant (d) X-linked recessive

Description : n the following human pedigree, the filled symbols represent the affected individuals. Identify the type of given pedigree. (i) (ii) (iii) (iv) (a) Autosomal recessive (b) X-linked dominant (c) Autosomal dominant (d) X-linked recessive

Last Answer : (a) Autosomal recessive

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

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.

.A diseased man marries a normal woman. They get three daughters and five sons. All the daughters were diseased and sons were normal. The gene of this disease is (a) sex linked dominant (b) sex linked recessive (c) sex limited character (d) autosomal dominant.

Description : .A diseased man marries a normal woman. They get three daughters and five sons. All the daughters were diseased and sons were normal. The gene of this disease is (a) sex linked dominant (b) sex linked recessive (c) sex limited character (d) autosomal dominant.

Last Answer : (a) sex linked dominant

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.

What is an autosomal dominant pattern of inheritance?

Description : What is an autosomal dominant pattern of inheritance?

Last Answer : Need answer

Which one is the incorrect statement with regard to the importance of pedigree analysis? (a) It confirms that DNA is the carrier of genetic information. (b) It helps to understand whether the trait in question is dominant or recessive. (c) It confirms that the trait is linked to one of the autosome. (d) It helps to trace the inheritance of a specific trait.

Description : Which one is the incorrect statement with regard to the importance of pedigree analysis? (a) It confirms that DNA is the carrier of genetic information. (b) It helps to understand whether the trait in ... linked to one of the autosome. (d) It helps to trace the inheritance of a specific trait.

Last Answer : (a) It confirms that DNA is the carrier of genetic information.

When dominant and recessive alleles express itself together it is called (a) co-dominance (b) dominance (c) amphidominance (d) pseudodominance.

Description : When dominant and recessive alleles express itself together it is called (a) co-dominance (b) dominance (c) amphidominance (d) pseudodominance.

Last Answer : (a) co-dominance

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.

Haploids are able to express both recessive and dominant alleles/mutations because there are (a) many alleles for each gene (b) two alleles for each gene (c) only one allele for each gene in the individual (d) only one allele in a gene.

Description : Haploids are able to express both recessive and dominant alleles/mutations because there are (a) many alleles for each gene (b) two alleles for each gene (c) only one allele for each gene in the individual (d) only one allele in a gene.

Last Answer : (c) only one allele for each gene in the individual

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

All are true about lesch-nyhan syndrome except (A) Produces self-mutilation (B) Genetic deficiency of the enzyme (C) Elevated levels of uric acid in blood (D) Inheritance is autosomal recessive

Description : All are true about lesch-nyhan syndrome except (A) Produces self-mutilation (B) Genetic deficiency of the enzyme (C) Elevated levels of uric acid in blood (D) Inheritance is autosomal recessive

Last Answer : Answer : B

All of the following statements about Tangier disease are true except (A) It is a disorder of HDL metabolism (B) Its inheritance is autosomal recessive (C) Apoproteins A-I and A-II are not synthesised (D) Plasma HDL is increased

Description : All of the following statements about Tangier disease are true except (A) It is a disorder of HDL metabolism (B) Its inheritance is autosomal recessive (C) Apoproteins A-I and A-II are not synthesised (D) Plasma HDL is increased

Last Answer : Answer : D

Which of the following is a characteristic feature of acute intermittent porphyria? 1) autosomal recessive inheritance 2) excessive faecal protoporphyrin excretion 3) excessive urinary porphobilinigoen between acute attacks 4) hypernatraemia during attacks 5) photosensitivity

Description : Which of the following is a characteristic feature of acute intermittent porphyria? 1) autosomal recessive inheritance 2) excessive faecal protoporphyrin excretion 3) excessive urinary porphobilinigoen between acute attacks 4) hypernatraemia during attacks 5) photosensitivity

Last Answer : Answers-3 Features of acute intermittent porphyria include urinary porphobilinogen excretion raised between attacks, hyponatraemia during an acute attack and autosomal dominant inheritance.

Which of the following is true of Gilbert's syndrome? 1) inheritance is autosomal recessive 2) serum conjugated bilirubin levels are elevated 3) serum bilirubin levels are decreased by fasting 4) serum bilirubin levels are decreased by liver enzyme inducers 5) there is bilirubinuria

Description : Which of the following is true of Gilbert's syndrome? 1) inheritance is autosomal recessive 2) serum conjugated bilirubin levels are elevated 3) serum bilirubin levels are decreased by fasting 4) serum bilirubin levels are decreased by liver enzyme inducers 5) there is bilirubinuria

Last Answer : Answers-4 Gilbert's syndrome is inherited in autosomal dominant fashion and affects 2-5% of the population. UDP glucuronyl transferase levels are reduced leading to an unconjugated hyperbilirubinaemia. ... the bilirubin is reabsorbed in the proximal tubule some bilirubin is detectable in the urine.

In autosomal recessive inheritance: a. the rarer the trait the higher the possibility of marriages within the same family b. most recessive gene defects cause problem through failure to produce functional protein c. both males and females are affected equally severely d. all above

Description : In autosomal recessive inheritance: a. the rarer the trait the higher the possibility of marriages within the same family b. most recessive gene defects cause problem through failure to produce functional protein c. both males and females are affected equally severely d. all above

Last Answer : all above

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.

Which one of the following cannot be explained on the basis of Mendel’s law of dominance? (a) The discrete unit controlling a particular character is called a factor. (b) Out of one pair of factors one is dominant, and the other recessive. (c) Alleles do not show any blending and both the characters recover as such in F2 generation. (d) Factors occur in pairs.

Description : Which one of the following cannot be explained on the basis of Mendel's law of dominance? (a) The discrete unit controlling a particular character is called a factor. (b) Out of one pair of ... any blending and both the characters recover as such in F2 generation. (d) Factors occur in pairs.

Last Answer : (c) Alleles do not show any blending and both the characters recover as such in F2 generation

All the following statements about xeroderma pigmentosum are true except (A) It is a genetic disease (B) Its inheritance is autosomal dominant (C) uvr ABC excinuclease is defective in this disease (D) It results in multiple skin cancers

Description : All the following statements about xeroderma pigmentosum are true except (A) It is a genetic disease (B) Its inheritance is autosomal dominant (C) uvr ABC excinuclease is defective in this disease (D) It results in multiple skin cancers

Last Answer : Answer : B

Which of the following is a characteristic feature of familial hypercholesterolaemia? 1) Autosomal dominant inheritance 2) elevated chylomicrons 3) hypertriglyceridaemia 4) increased expression of LDL receptors 5) Palmar xanthomas

Description : Which of the following is a characteristic feature of familial hypercholesterolaemia? 1) Autosomal dominant inheritance 2) elevated chylomicrons 3) hypertriglyceridaemia 4) increased expression of LDL receptors 5) Palmar xanthomas

Last Answer : Answers-1 Familial hypercholesterolaemia is an autosomal dominant condition manifest by increased LDL concentrations (not chylomicrons) due to constitutional abnormalities and reduced numbers of ... are characteristic and the condition is associated with a premature cardiovascular mortality.

Which of the following is a characteristic feature of familial hypercholesterolaemia? 1) Autosomal dominant inheritance 2) elevated chylomicrons 3) hypertriglyceridaemia 4) increased expression of LDL receptors 5) Palmar xanthomas

Description : Which of the following is a characteristic feature of familial hypercholesterolaemia? 1) Autosomal dominant inheritance 2) elevated chylomicrons 3) hypertriglyceridaemia 4) increased expression of LDL receptors 5) Palmar xanthomas

Last Answer : Answers-1 Familial hypercholesterolaemia is an autosomal dominant condition manifest by increased LDL concentrations (not chylomicrons) due to constitutional abnormalities and reduced numbers of ... are characteristic and the condition is associated with a premature cardiovascular mortality.

What is the difference between dominant and recessive alleles?

Description : What is the difference between dominant and recessive alleles?

Last Answer : Dominant alleles are expressed when present in either one or both copies, while recessive alleles are only expressed when present in both copies.

A plant has two alleles for color. The red allele is recessive, and is represented by q. The purple allele is dominant, and is represented by p. If 30 of 100 organisms are red, what is q?

Description : A plant has two alleles for color. The red allele is recessive, and is represented by q. The purple allele is dominant, and is represented by p. If 30 of 100 organisms are red, what is q?

Last Answer : 0.55

A fly has two alleles for the color of its eyes. The green allele is recessive, and is represented by q. The blue allele is dominant, and is represented by p. If 20 of 100 organisms are green, what is q?

Description : A fly has two alleles for the color of its eyes. The green allele is recessive, and is represented by q. The blue allele is dominant, and is represented by p. If 20 of 100 organisms are green, what is q?

Last Answer : A. 0.45 Apex

If one parent has two dominant alleles and another parent has two recessive alleles the offspring will have?

Description : If one parent has two dominant alleles and another parent has two recessive alleles the offspring will have?

Last Answer : PFHHHHH

A species of flu has two alleles for the length of their legs. The allele for long leg is dominant, and is represented by p. The allele for short legs is recessive, and is represented by q. If 33 of 100 organisms have short legs, what is p?

Description : A species of flu has two alleles for the length of their legs. The allele for long leg is dominant, and is represented by p. The allele for short legs is recessive, and is represented by q. If 33 of 100 organisms have short legs, what is p?

Last Answer : 0.043

A species of flu has two alleles for the length of their legs. The allele for long leg is dominant, and is represented by p. The allele for short legs is recessive, and is represented by q. If 33 of 100 organisms have short legs, what is p?

Description : A species of flu has two alleles for the length of their legs. The allele for long leg is dominant, and is represented by p. The allele for short legs is recessive, and is represented by q. If 33 of 100 organisms have short legs, what is p?

Last Answer : 0.043

The principle of dominance states that a. all alleles are dominant. b. all alleles are recessive. c. some alleles are dominant and others are recessive. d. alleles are neither dominant nor recessive.

Description : The principle of dominance states that a. all alleles are dominant. b. all alleles are recessive. c. some alleles are dominant and others are recessive. d. alleles are neither dominant nor recessive.

Last Answer : c. some alleles are dominant and others are recessive.

. 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

All the following statements about primary gout are true except (A) Its inheritance is X-linked recessive (B) It can be due to increased activity of PRPP synthetase (C) It can be due to increased activity of hypoxanthine guanine phosphoribosyl transferase (D) De novo synthesis of purines is increased in it

Description : All the following statements about primary gout are true except (A) Its inheritance is X-linked recessive (B) It can be due to increased activity of PRPP synthetase (C) It can be ... activity of hypoxanthine guanine phosphoribosyl transferase (D) De novo synthesis of purines is increased in it

Last Answer : Answer : C

Haemophilia is more commonly seen in human males than in human females because (a) a greater proportion of girls die in infancy (b) this disease is due to a Y-linked recessive mutation (c) this disease is due to an X-linked recessive mutation (d) this disease is due to an X-linked dominant mutation.

Description : Haemophilia is more commonly seen in human males than in human females because (a) a greater proportion of girls die in infancy (b) this disease is due to a Y-linked recessive mutation (c) this ... to an X-linked recessive mutation (d) this disease is due to an X-linked dominant mutation.

Last Answer : this disease is due to an X-linked recessive mutation

Which of the following most appropriately describes haemophilia? (a) Chromosomal disorder (b) Dominant gene disorder (c) Recessive gene disorder (d) X-linked recessive gene disorder

Description : Which of the following most appropriately describes haemophilia? (a) Chromosomal disorder (b) Dominant gene disorder (c) Recessive gene disorder (d) X-linked recessive gene disorder

Last Answer : (d) X-linked recessive gene disorder

A genetically diseased father (male) marries with a normal female and gives birth to 3 carrier girls and 5 normal sons. It may be which type of genetic disease? (a) Sex-influenced disease (b) Blood group inheritance disease (c) Sex-linked disease (d) Sex-recessive disease

Description : A genetically diseased father (male) marries with a normal female and gives birth to 3 carrier girls and 5 normal sons. It may be which type of genetic disease? (a) Sex-influenced disease (b) Blood group inheritance disease (c) Sex-linked disease (d) Sex-recessive disease

Last Answer : (c) Sex-linked disease

RR (Red) Antirrhinum is crossed with white (WW) one. Offspring RW are pink. This is an example of (a) dominant-recessive (b) incomplete dominance (c) hybrid (d) supplementary genes.

Description : RR (Red) Antirrhinum is crossed with white (WW) one. Offspring RW are pink. This is an example of (a) dominant-recessive (b) incomplete dominance (c) hybrid (d) supplementary genes.

Last Answer : (b) incomplete dominance

5 Consider a cross in which a trait is inherited by incomplete dominance. What percentage of the F2 from the matng of homozygous dominant and homozygous recessive individuals will possess the dominant phenotype?

Description : 5 Consider a cross in which a trait is inherited by incomplete dominance. What percentage of the F2 from the matng of homozygous dominant and homozygous recessive individuals will possess the dominant phenotype? a) 0 per cent b) 25 per cent c) 50 per cent d) 75 per cent

Last Answer : ANS: b 25 per cent

With regard to blood groups and blood products: a. the ABO system is inherited in an autosomal dominant pattern b. group O and Rhesus positive is the universal donors' blood. c. stored whole blood contains dextrose, phosphate and citrate d. stored blood becomes progressively more acidotic and hyperkalaemic with time

Description : With regard to blood groups and blood products: a. the ABO system is inherited in an autosomal dominant pattern b. group O and Rhesus positive is the universal donors' blood. ... dextrose, phosphate and citrate d. stored blood becomes progressively more acidotic and hyperkalaemic with time

Last Answer : stored blood becomes progressively more acidotic and hyperkalaemic with time

Select the incorrect statement with regard to haemophilia. (a) It is a dominant disease.(b) A single protein involved in the clotting of blood is affected. (c) It is a sex-linked disease. (d) It is a recessive disease.

Description : Select the incorrect statement with regard to haemophilia. (a) It is a dominant disease. (b) A single protein involved in the clotting of blood is affected. (c) It is a sex-linked disease. (d) It is a recessive disease.

Last Answer : (a) It is a dominant disease.

.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)

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 idea is depicted by a cross in which the F1 generation resembles both the parents? (a) Inheritance of one gene (b) Co-dominance (c) Incomplete dominance (d) Complete dominance

Description : Which idea is depicted by a cross in which the F1 generation resembles both the parents? (a) Inheritance of one gene (b) Co-dominance (c) Incomplete dominance (d) Complete dominance

Last Answer : (b) Co-dominance

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

Which of the following diseases is a chronic, progressive, hereditary disease of the nervous system that results in progressive involuntary dance-like movement and dementia? a) Huntington’s disease Because it is transmitted as an autosomal dominant genetic disorder, each child of a parent with HD has a 50% risk of inheriting the illness.

Description : Which of the following diseases is a chronic, progressive, hereditary disease of the nervous system that results in progressive involuntary dance-like movement and dementia? a) Huntington's ... the central nervous system characterized by spongiform degeneration of the gray matter of the brain.

Last Answer : a) Huntington’s disease Because it is transmitted as an autosomal dominant genetic disorder, each child of a parent with HD has a 50% risk of inheriting the illness.

Autosomal recessive?

Description : Autosomal recessive?

Last Answer : DefinitionAutosomal recessive is one of several ways that a trait, disorder, or disease can be passed down through families.An autosomal recessive disorder means two copies of an abnormal gene must be ... be defective to cause disease. People with only one defective gene in the pair are considered

An autosomal recessive disorder, xanthinuria is due to deficiency of the enzymes: (A) Adenosine deaminase (B) Xanthine oxidase (C) HGPRTase (D) Transaminase

Description : An autosomal recessive disorder, xanthinuria is due to deficiency of the enzymes: (A) Adenosine deaminase (B) Xanthine oxidase (C) HGPRTase (D) Transaminase

Last Answer : Answer : B

All the following statements about cystic fibrosis are correct except (A) It is inherited as an autosomal recessive disease (B) It affects a number of exocrine glands (C) It causes increased sweating (D) Sweat chlorides are above 60 mEq/L in this disease

Description : All the following statements about cystic fibrosis are correct except (A) It is inherited as an autosomal recessive disease (B) It affects a number of exocrine glands (C) It causes increased sweating (D) Sweat chlorides are above 60 mEq/L in this disease

Last Answer : Answer : C

Albinism is known to be due to an autosomal recessive mutation. The first child of a couple with normal skin pigmentation was an albino. What is the probability that their second child will also be an albino? (a) 50% (b) 75% (c) 100% (d) 25%

Description : Albinism is known to be due to an autosomal recessive mutation. The first child of a couple with normal skin pigmentation was an albino. What is the probability that their second child will also be an albino? (a) 50% (b) 75% (c) 100% (d) 25%

Last Answer : (d) 25%