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Sindh Mdcat Exclusive Course Biology Inheritance — Solved Past Paper with Answers

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Q1. In the pedigree of a family shown above, brown eyes are indicated as white circles and blue eyes as dark circles. Javeria and Juhi are twins. From this chart, it can be determined that:

  • A. Tahir and Mary are homozygous for brown eyes
  • B. Jawaria and Juhi are identical twins
  • C. Juhi is heterozygous for blue eyes
  • D. Juhi is homozygous for blue eyes
  • E. Jawaria and Saad are homozygous for brown eyes

Explanation: It is imperative for a recessive trait present in a homozygous state to show up in phenotype so answer D is correct.

Why the other options are wrong
  • A. Option A is wrong because if they would have been homozygous then they couldn't produce a child having blue eyes (which is a recessive trait), rather they are a confirmed case of heterozygous
  • B. Option B is wrong because genotypically in identical twins not even a single gene can differ and Jawaria and Juhi have differences in genes of eye color.
  • C. Option C is wrong as Juhi can not be heterozygous for blue eyes as a recessive trait should always be homozygous to be expressed in phenotype.
  • E. Option E is wrong because Jawaria and Saad can be both homozygous or heterozygous for brown eyes as their parents are heterozygous. So it cannot be predicted from the diagram shown.

Q2. Which trait is not sex-linked recessive:

  • A. Haemophilia
  • B. Colour blindness
  • C. Hypophosphatemia
  • D. TFM syndrome

Explanation: This is correct answer as hypophosphatemia is an sex-linked dominant disease not recessive.

Why the other options are wrong
  • A. Haemophilia is a sex-linked recessive disorder, primarily affecting males, because the gene causing haemophilia is located on the X chromosome.
  • B. Colour blindness, particularly red-green colour blindness, is a sex-linked recessive trait found on the X chromosome.
  • D. Testicular feminization syndrome (TFM), also known as Androgen Insensitivity Syndrome, is a sex-linked recessive disorder. It is caused by mutations in the androgen receptor gene on the X chromosome.

Q3. The gene which controls the ABO group has how many alleles in an individual?

  • A. 1
  • B. 2
  • C. 3
  • D. 4

Explanation: 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. However, a single individual has two ABO blood type alleles, because we each inherit one blood type allele from our biological mother and one from our biological father. Hence, the correct answer is B.

Why the other options are wrong
  • A. This option is not correct.we have only 2 genes for blood group. because one person can have only 2 alleles at a time
  • C. we have only 2 genes for blood group. because one person can have only 2 alleles at a time
  • D. This option is not correct. we have only 2 genes for blood group. because one person can have only 2 alleles at a time

Q4. A pure breeding plant with the dominant phenotype of character P and the recessive phenotype of character Q was crossed with another pure breeding plant with the recessive phenotype of character P and the dominant phenotype of Q. The offspring of this cross were crossed with a double homozygous recessive for P and Q and the following results were obtained:22 were phenotypically dominant for P and recessive for Q5 were phenotypically dominant for both P and Q4 were phenotypically recessive for both P and Q24 were phenotypically recessive for P and dominant for QWhich one of the following types of Inheritance is illustrated by these results?

  • A. Gene linkage of P and Q
  • B. Independent segregation of P and Q
  • C. Mendelian dihybrid Inheritance
  • D. Multiple alleles
  • E. Polygenic Inheritance

Explanation: When a pure breeding phenotypic dominant character P and recessive character Q is crossed with pure breeding recessive character P and dominant character Q, the cross is below:- PPqq X ppQQ will give PpQq. Now when this PpQq is crossed with recessive for both:- PpQq X ppqq will give PpQq ; Ppqq ; ppqq ; ppQq The ratio when there is a dihybrid cross between heterozygous character and homozygous recessive character is 9:3:3:1. However, the above ratio is not consistent with what it should be. This happens when there is a gene linkage between two characters

Why the other options are wrong
  • B. the process of random segregation and assortment of pairs of alleles during gamete formation will result in the production of gametes with all possible allele combinations in equal numbers.
  • C. Dihybrid crosses are visual representations of the inheritance of the different versions of these genes, termed “alleles.” According to the law of independent assortment of Mendelian inheritance, alleles of different genes are inherited independently of each other.
  • D. Multiple alleles can be defined as a series of forms of a gene situated at the same locus of homologous chromosomes. According to Mendel, each gene had two alternate forms or allele morphs are being dominant and the other being recessive.
  • E. “Polygenic inheritance is defined as quantitative inheritance, where multiple independent genes have an additive or similar effect on a single quantitative trait.” Polygenic inheritance is also known as multiple gene inheritance or multiple factor inheritance.

Q5. Flower color is controlled by a single pair of alleles. The allele for red flowers is dominant to the allele for white flowers. A plant homozygous for red flowers is crossed with a plant homozygous for white flowers. All the resulting plants have red flowers (F1 generation). When the F1 generation crosses with each other, 18 plants are obtained. 12 plants have red flowers and 6 have white flowers (F2 generation). What ratio is expected in the F2 generation and what ratio has been obtained?

  • A. 3:1 expected, 2:1 obtained
  • B. 2:1 expected, 3:1 obtained
  • C. 1:1 expected, 3:1 obtained
  • D. 1:1 expected, 2:1 obtained

Explanation: The correct answer is that the expected ratio in the F2 generation is 3:1, and the obtained ratio is 2:1. In a typical Mendelian monohybrid cross (Rr x Rr), the expected phenotypic ratio is 3:1, with three plants having the dominant phenotype (red flowers) for every one plant with the recessive phenotype (white flowers). The obtained ratio of 2:1 suggests a deviation from the expected, possibly due to a small sample size or experimental error. The other options incorrectly present the expected and obtained ratios.

Why the other options are wrong
  • B. This option confuses the expected and obtained ratios. The Mendelian expectation is 3:1, not 2:1, and the actual result was 2:1, not 3:1.
  • C. The expected ratio in a typical Mendelian cross involving a heterozygous pair is 3:1, not 1:1. The obtained ratio of 2:1 also does not match 3:1.
  • D. This option incorrectly assumes a 1:1 expected ratio, which is not typical for a heterozygous cross like Rr x Rr, where the expected ratio is 3:1.

Q6. Consider the following statements about biological communities.I. Their members share a common gene poolII. The community remains stable even though some physical aspect of the environment may undergo a changeIII. It consists of all the populations living in a particular area.IV. A community interacts with a non-living environment and both function together to form an ecosystemWhich two of the above statements are true?

  • A. 1 and 2
  • B. 1 and 3
  • C. 2 and 4
  • D. 2 and 3
  • E. 3 and 4

Explanation: Different living and nonliving things in a single habitat form a single community. Since different species are present they have different characteristics so the gene pool is not the same. Change in the environment does cause a change in the balance of genes in the environment so the community does not remain stable.The last two statements iii and iv are right that as previously mentioned the community is all the population living in a particular area. Secondly, the community involves biotic(living) and abiotic(non-living) factors interacting with one another.

Why the other options are wrong
  • A. A community includes many different species (plants, animals, microbes, etc.), each with its own gene pool. The idea of a common gene pool applies only to a population (members of one species), not to a community containing many populations..
  • B. Biological communities tend to maintain a dynamic stability. Even when physical conditions (like temperature or rainfall) change slightly, the community can adapt through species interactions, balance between producers and consumers, and natural resilience.
  • C. This is the definition of a biological community — all the different populations of species that live and interact in a specific area form a community.
  • D. This describes the ecosystem, not the community itself. A community is the living part, while the ecosystem includes both biotic and abiotic components.

Q7. In birds the male is the homogametic sex. A male bird showing the recessive trait was mated with a female showing the dominant trait of a characteristic governed by a pair of alleles which are sex-linked. What is the probability that the male offspring will show the dominant trait?

  • A. 0
  • B. 0.25
  • C. 0.50
  • D. 0.75
  • E. 1.00

Explanation: In this problem, we are dealing with a sex-linked trait where the male parent (XbY) carries the recessive allele (b), and the female parent (XBXB) has two dominant alleles (B). The key is to recognize that in birds, males are homogametic, meaning they have two identical sex chromosomes (XY), while females have two different sex chromosomes (XX).The cross between the male (XbY) and the female (XBXB) yields the following gametes:Xb from the male and XB from the female leads to XbXB (female with dominant trait)Xb from the male and XB from the female leads to XbXB (female with dominant trait)Y from the male and XB from the female leads to XBY (male with dominant trait)Y from the male and XB from the female leads to XBY (male with dominant trait)Thus, all male offspring (XBY) will inherit the dominant allele from the mother, resulting in a probability of 1.00 that they will express the dominant trait.The other options are incorrect because they misinterpret the inheritance pattern and the genotypes of the parents involved in the cross.

Why the other options are wrong
  • A. There is no chance of male offspring showing the dominant trait since both parents must provide a dominant allele for the trait to be expressed.
  • B. This option implies that there is a 25% chance for male offspring to show the dominant trait, which is incorrect based on the provided genotypes.
  • C. A 50% probability suggests that half of the male offspring would show the dominant trait, which does not align with the outcomes from the cross.
  • D. This option indicates a 75% chance of male offspring exhibiting the dominant trait, which is also incorrect given the specific genotypes and inheritance pattern.

Q8. “Law of independent assortment” states:

  • A. That each pair of alleles assort independently of other pairs of alleles during gamete formation
  • B. That alleles of each pair of contrasting trait have unequal probability to assort with the alleles of other pair
  • C. That the two coexisting alleles for each trait segregate (separate) from each other at meiosis so that each gamete receives only one of the two alleles
  • D. That pertain to inheritance of single trait (monohybrid cross)

Explanation: Mendel's law of independent assortment states that the alleles of two (or more) different genes get sorted into gametes independently of one another. In other words, the allele a gamete receives for one gene does not influence the allele received for another gene.

Why the other options are wrong
  • B. This statement is not accurate. The Law of Independent Assortment states that alleles segregate independently, regardless of the alleles at other gene loci. The probability of assorting is equal for all alleles.
  • C. This statement describes the Law of Segregation, not the Law of Independent Assortment. The Law of Segregation states that each individual has two alleles for each gene, and these alleles segregate during the formation of gametes.
  • D. The Law of Independent Assortment is not specific to a single trait but applies to genes located on different chromosomes. The term "monohybrid cross" is more closely associated with the Law of Segregation.

Q9. In 'Complete Dominance':

  • A. Different alleles of a gene are both expressed in heterozygous condition
  • B. One allele (R) is completely dominant over the other (r)
  • C. The phenotype of the heterozygote is intermediate between phenotypes of the two homozygotes
  • D. Gene mutations may produce many different alleles of a gene

Explanation: Complete dominance is a form of dominance in a heterozygous condition wherein the allele that is regarded as dominant completely masks the effect of the allele that is recessive. Option C refers to 'Incomplete Dominance' where a dominant allele, or form of a gene, does not completely mask the effects of a recessive allele, and the organism's resulting physical appearance shows a blending of both alleles.

Why the other options are wrong
  • A. This describes codominance, not complete dominance.In codominance, both alleles in a heterozygote are fully expressed — for example, in human AB blood group, both A and B alleles are expressed equally.However, in complete dominance, only one allele (the dominant one) shows its effect, while the recessive allele is completely masked.
  • C. This describes incomplete dominance, not complete dominance.In incomplete dominance, neither allele is completely dominant; the heterozygous phenotype is a blend of both alleles.Example:In snapdragon flowers, a red (RR) and white (rr) parent produce pink (Rr) offspring.
  • D. While gene mutations can indeed create multiple alleles, this has no relation to the concept of complete dominance.Complete dominance only describes how two existing alleles interact, not how alleles are formed through mutation.

Q10. Which statement about dominant and recessive alleles is not correct?

  • A. A dominant characteristic is seen in the phenotype of a heterozygote.
  • B. A homozygous genotype may be either dominant or recessive.
  • C. Recessive phenotypes always have two recessive alleles.
  • D. The phenotype of a homozygote is always dominant.

Explanation: Phenotype of a homozygote can be dominant or recessive both AA or aa. Hence statement D is incorrect and our answer.

Why the other options are wrong
  • A. This statement is correct. In a heterozygote (e.g., Aa), the dominant allele (A) will determine the phenotype, masking the effect of the recessive allele (a).
  • B. This statement is correct. Homozygous genotypes can be either dominant (AA) or recessive (aa), depending on the alleles present.
  • C. This statement is correct. A recessive phenotype appears only when the individual has two recessive alleles (aa).

Q11. Pick the correct option for Drosophila.

  • A. The Male is larger with a pointed abdomen
  • B. The female has sex combs on its front legs
  • C. It has a generation time of just eight weeks
  • D. Salivary gland cells have giant chromosomes in their nuclei

Explanation: Polytene chromosomes form in the Drosophila giant salivary gland during development by multiple rounds of genome replication without cell division to generate polytene chromosomes containing up to 1000 copies of DNA per chromosome.

Why the other options are wrong
  • A. In Drosophila (fruit fly), females are larger than males and have a pointed abdomen.Males, on the other hand, are smaller, have a rounded and darker abdomen, and possess sex combs on their forelegs.Hence, this statement is the reverse of the truth.
  • B. Sex combs are distinctive bristle-like structures found only in male Drosophila on their front legs.They are used during mating to grasp the female.Therefore, the statement that females have sex combs is wrong — only males have them.
  • C. The generation time of Drosophila (the time from egg to adult) is about two weeks (10–14 days) under optimal conditions at room temperature.This short life cycle makes it a popular model organism in genetics research.Eight weeks would be far too long for Drosophila.

Q12. J. Seiler in 1914 discovered which type of sex determination in moths?

  • A. XO - XX
  • B. XY - XX
  • C. ZZ - ZW
  • D. None of the given options

Explanation: Even when two W chromosomes are paired to one Z chromosome in W 1W 2Z/ZZ systems, sex chromosome separation appears to be precise.

Why the other options are wrong
  • A. XO - XX Type This pattern of sex determination is found in grasshoppers and Protenor bugs.
  • B. XY-XX Type: This pattern of sex determination is found in Drosophila, man, and many other organisms.
  • D. This could not be the ans because J. Seilar discovered the ZZ-ZW sex determination system.

Q13. Discontinuous variations in a population were first observed by:

  • A. Mendel
  • B. Correns
  • C. Nilsson
  • D. Darwin

Explanation: Mendel's concept of the gene was based on the analysis of hereditary variants—organisms that show identifiable and persistent differences for specific characters. He was the first to establish rules for the genetic analysis of such distinct variants.

Why the other options are wrong
  • B. He rediscovered and independently verified the work of Mendel in a separate model organism. He also discovered cytoplasmic inheritance, an important extension of Mendel's theories, which demonstrated the existence of extra-chromosomal factors on phenotype.
  • C. Nils Herman Nilsson-Ehle. , advanced the "multiple factor" theory, or theory of polygenic inheritance, in which a trait is produced from the cumulative effects of more than one gene. Traits that display a continuous distribution, such as height, hair or skin color, are polygenic.
  • D. Darwin is most famous for writing a book called 'On the Origin of Species'. It talked about evolution and how species had changed and developed over time. 7. His ideas were not accepted by everyone at first.

Q14. The genotype of blood group 'AB' in humans is _.

  • A. IA IB
  • B. IB Io
  • C. IA IA
  • D. IoIo

Explanation: ABO blood type in humans is determined by 3 alleles IA, IB (Dominant), and i (Recessive) Genotype IA shows blood group A. Genotype TB shows blood group B. Genotype Io shows blood group O. But, IA & IB are co-dominant alleles means neither of the dominant alleles can mask the expression of other dominant alleles. So, the genotype IA IB shows blood group AB.

Why the other options are wrong
  • B. This genotype represents blood group B, as it has the B allele from one parent and an O allele from the other parent.
  • C. This genotype represents blood group A, as it has the A allele from both parents.
  • D. This genotype represents blood group O, as it has an O allele from both parents.

Q15. Which one is not a continuous trait?

  • A. Human height
  • B. Tongue rolling
  • C. Wheat grain color
  • D. Human skin color

Explanation: A continuous trait displays a range of expression (such as weight, height, etc.) rather than an all-or-none appearance (such as white or red)

Why the other options are wrong
  • A. Human height has a range of valuesHuman height is often treated as a continuous trait, meaning that it exists on a spectrum and can vary across a range of values. In a given population, you can typically observe a distribution of heights where individuals fall along a continuum from shorter to taller. The continuous nature of height is a result of the polygenic inheritance pattern, which means that multiple genes contribute to determining a person's height. These genes interact with each other and with environmental factors, such as nutrition and health, to influence the final outcome. While height is predominantly continuous, it is often convenient to categorize individuals into discrete groups for certain purposes, such as clinical assessments or statistical analysis. These categories, such as "tall," "average," and "short," are arbitrary thresholds imposed on a continuous trait for convenience or specific applications. However, it is important to note that these categories are not universally defined and can vary across cultures and contexts.
  • C. Wheat grain colour has a range of coloursWheat grain color is typically considered a discrete trait rather than a continuous trait. Wheat grain color can vary among different varieties and can be classified into distinct categories such as red, white, or yellow, among others. The color of wheat grain is determined by the presence or absence of specific pigments, such as anthocyanins or carotenoids, which are influenced by genetic factors. Different alleles at specific gene loci can result in variations in grain color. For example, in some cases, the presence of pigments leads to red or dark-colored grains, while the absence of pigments results in white or yellow grains. While there can be some variation within each color category, the overall categorization of wheat grain color into discrete groups is commonly used in agricultural research, breeding programs, and the industry. This discrete classification allows for easier identification, selection, and breeding of wheat varieties with specific grain colors to meet various market demands or agronomic requirements.
  • D. Human skin colour has a range of coloursHuman skin color is a complex trait influenced by multiple genetic and environmental factors. It exhibits a wide range of variation across populations, and this variation is often described as a continuum rather than discrete categories. The color of human skin is primarily determined by the amount and distribution of a pigment called melanin, which is produced by specialized cells called melanocytes. Melanin comes in two main forms: eumelanin, which is brown-black, and pheomelanin, which is yellow-red. The relative proportions and distribution of these two types of melanin, along with other factors such as blood flow and collagen content, contribute to the observed variation in skin color. Skin color is influenced by multiple genes, and variations in these genes can lead to differences in the production, distribution, and activity of melanin. However, the inheritance of skin color is not as straightforward as a single gene with clear dominant or recessive alleles. Instead, it involves the interaction of multiple genes and complex inheritance patterns. Due to the continuous nature of human skin color variation, it is often more accurate to describe it as a spectrum or gradient rather than discrete categories. The concept of discrete racial or ethnic categories based on skin color is a social construct that does not fully capture the complexity and diversity of human populations.

Q16. Linked genes with closer loci _ Mendel’s law of independent assortment as they _ assort independently.

  • A. Don’t obey:cannot
  • B. Don’t obey:can
  • C. obey:cannot
  • D. obey:can

Explanation: Mendel's law of independent assortment states that the alleles of two (or more) different genes get sorted into gametes independently of one another

Why the other options are wrong
  • B. Mendel’s law states that independent assortment takes place hence if it could assort independently, it would obey the law
  • C. Mendel’s law states that independent assortment takes place hence if it could assort independently, it would obey the law
  • D. They do not obey the law

Q17. Ahmed’s blood CANNOT clot properly; he was diagnosed with hemophilia A. He passed this trait to his grandson through his:

  • A. Wife
  • B. Son
  • C. Daughter
  • D. Brother

Explanation: X chromosome of the father is only transferred to the daughter, son takes the Y chromosome and haemophilia is a X-linked diseaseAhmed, who has hemophilia A, a condition where blood does not clot properly, can pass this trait to his grandson through his daughter. Hemophilia A is an X-linked recessive disorder, meaning that the gene responsible for the condition is located on the X chromosome.Since Ahmed is the grandfather, he must pass on his X chromosome to his daughter. If his daughter inherits the affected X chromosome from Ahmed, she becomes a carrier of hemophilia A. As a carrier, she has one normal X chromosome and one affected X chromosome, but since hemophilia A is a recessive trait, she does not show symptoms of the condition.When the daughter has a child (Ahmed's grandson), she has a 50% chance of passing on the affected X chromosome to her son. If the affected X chromosome is passed on, the grandson would inherit the hemophilia A trait and potentially experience clotting problems.It's important to note that if the daughter does not pass on the affected X chromosome to her son, he will not inherit hemophilia A. However, he would still be a carrier of the condition, meaning he could potentially pass it on to his own offspring if he has children in the future.

Why the other options are wrong
  • A. The wife is not Ahmed’s offspring, and the question asks how Ahmed passed the trait to his grandson.Although the wife provides X chromosomes to her own children, Ahmed’s hemophilia gene must be transmitted through his own X chromosome, not via his wife.So, this option is irrelevant.
  • B. A son inherits the Y chromosome from his father and the X chromosome from his mother.Since hemophilia A is X-linked recessive, Ahmed’s X chromosome (with the defective gene) cannot go to his son — it only goes to his daughter.Hence, Ahmed cannot pass hemophilia directly to his son.
  • D. Ahmed’s brother is not his descendant, and therefore Ahmed cannot pass the gene through him.This option is unrelated to the inheritance line leading to Ahmed’s grandson.

Q18. A continuously varying trait is encoded by alleles of two or more different genes located at different loci, all influencing the same trait in an additive way is known as _.

  • A. Polytraits
  • B. Polygenes
  • C. Multiple alleles
  • D. Different genes
  • E. Allele frequency

Explanation: Polygenic inheritance is a type of inheritance where a continuously varying trait is influenced by alleles of two or more different genes located at different loci. These alleles are said to be polygenes, and they all contribute to the phenotype of the individual in an additive way. Examples of traits that are controlled by polygenes include height, skin color, and intelligence.

Why the other options are wrong
  • A. Poly traits, also known as polygenic traits, refer to traits that are controlled by multiple genes. These genes can be located at different loci and contribute to the trait's variation in an additive manner. Polytraits often result in a wide range of phenotypic variations.
  • C. Multiple alleles refer to more than two alleles of a gene in a population. Each individual can have only two alleles (one from each parent), but the population as a whole may have multiple alleles at a specific gene locus. Multiple alleles contribute to genetic diversity and can result in a range of phenotypic variations for a trait.
  • D. Different genes simply refer to genes that are distinct and separate from each other. They may or may not be related to the same trait or phenotype. The presence of different genes in an organism's genome contributes to its overall genetic makeup.
  • E. Allele frequency refers to the relative proportion or frequency of a specific allele within a population. It represents how common or rare a particular allele is in the population. Allele frequency is an important concept in population genetics and evolutionary studies.

Q19. The total number of genes present in a particular population, at a particular time is called:

  • A. Gene
  • B. Genome
  • C. Genotype
  • D. Gene Pool
  • E. Karyotype

Explanation: Gene pool refers to the sum total of all the genes, alleles, and their variations present in a population at a particular time. It includes all the genetic information and diversity available within a population. The gene pool of a population is subject to change due to various factors such as mutation, migration, genetic drift, and natural selection.

Why the other options are wrong
  • A. A gene is a specific segment of DNA that contains the instructions for building a particular protein or determining a specific trait. However, the total number of genes present in a population is not referred to as a "gene."
  • B. The genome refers to the complete set of genetic material (DNA) present in an organism. It includes all the genes, non-coding sequences, and regulatory elements. The genome encompasses the entire genetic information of an individual or a species.
  • C. Genotype refers to the genetic constitution of an individual, specifically the combination of alleles present in an organism's DNA. It represents the genetic information that determines the observable traits (phenotype) of an organism. However, the term "genotype" does not describe the total number of genes in a population.
  • E. A karyotype is a visual representation of the chromosomes of an individual or a species, arranged in a specific order. It allows for examining the number, structure, and size of chromosomes. While a karyotype provides valuable information about the organization of chromosomes, it does not describe the total number of genes in a population.

Q20. The type of gene interaction in which the effect caused by a gene at one locus interferes with the effect caused by another gene at another locus is known as:

  • A. Pleiotropy
  • B. Epistasis
  • C. Polygenic inheritance
  • D. Gene linkage
  • E. Crossing over

Explanation: Option A: Pleiotropy is a gene interaction in which a single gene affects multiple traits. Option B: The type of gene interaction in which the effect caused by a gene at one locus interferes with the effect caused by another gene at another locus is known as epistasis. Option C: Polygenic inheritance is a gene interaction in which multiple genes contribute to a single trait. Option D: Gene linkage is a phenomenon in which genes that are located close together on a chromosome are inherited together more often than would be expected by chance. Option E: Crossing over is a process that occurs during meiosis in which homologous chromosomes exchange genetic material.

Why the other options are wrong
  • A. Pleiotropy is a gene interaction in which a single gene affects multiple traits.
  • C. Polygenic inheritance is a gene interaction in which multiple genes contribute to a single trait.
  • D. Gene linkage is a phenomenon in which genes that are located close together on a chromosome are inherited together more often than would be expected by chance.
  • E. Crossing over is a process that occurs during meiosis in which homologous chromosomes exchange genetic material.

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