hich if the following is not among Mendels principles? a. There are factors that is transmitted from parent to offspring? b. There are only two kinds of traits, dominant and recessive c. Genes resides in the chromosome d. Pair of single traits segregate randomly

hich if the following is not among Mendels principles? a. There are factors that is transmitted from parent to offspring? b. There are only two kinds of traits, dominant and recessive c. Genes resides in the chromosome d. Pair of single traits segregate randomly

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter4: Pedigree Analysis In Human Genetics

Section: Chapter Questions

Problem 2CS: Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a...

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What is Mendel’s law of segregation? Allele pairs separate during the formation of gametes, and pair back up upon fertilisation. During meiosis, the alleles of two or more genes separate into the gametes independent of each other. During meiosis. genetic material segregates equally into the resulting gametes. The separation of alleles into different gametes results in genetically distinct offspring. During meiosis, genes that are in close proximity on the genome are more likely to cross over together.
Mendelian Genetics Consider blue eyes in a man as recessive to brown eyes. Show the expected children of a marriage between a blue-eyed woman and brown-eyed man who had a blue-eyed mother. Determine the genotypic ratio (GR) and phenotypic ratio (PR) of the F1 using Punnett Square Method. Hint: Determine the genotypes of each individual first.
Let us recall your understanding of concepts of Mendel’s law of inheritance by predicting the possible offspring on a test cross using a Punnett square: Red tomato fruit (R) is dominant over yellow fruit (r). In a test cross between a homozygous red tomato fruit plant and a tomato plant that has yellow fruit, what would be the genotypes of the parents? Genotype: Phenotype: Questions: a. What are the genotypes of the offspring? b. What are the phenotypes? c. If two of the F1 generation from the above cross were mated, what would be the phenotypes and genotypes of the offspring?
. When Mendel crossed a large number of tall pea plants with short pea plants, all F1 plants were tall. The F2 generation was created by self-pollinating the F1 plants. Complete a genetic cross of F2 to show the genotypes and phenotypes of the offspring. State the ratio of phenotypes expected in the F2 offspring. Mendel’s First Law of inheritance states that, “…the alleles of a given locus segregate into separate gametes.” Explain how the genetic diagram above proves this law. (AC 2.1) can i get help please.
Mendel examined two distinct flower phenotypes in his pea plants. Flower color and flower position. The violet color (W) is dominant over the white color (w), and the axial position (T) is dominant over terminal (t). Predict the F1 ratios of these phenotypes from a parent heterozygous for both traits and the other parent homozygous recessive for both traits. Show your work. Flower color Flower position violet/white axial/terminal
Which of the following statements describes Mendel’s Law of Segregation? a. The dominant allele is represented with an uppercase letter and the recessive allele is represented with a lowercase letter. b. A Punnett square can be used to predict the outcome of a parental cross. c. Dominant alleles are always expressed in a homozygous or heterozygous individual. d. A Bb individual will produce B and b alleles, while a bb individual will only produce a b allele.
Mendel's second postulate states: When two different unit factors responsible for a characteristic are found in the same organism, one will dominate and determine the characteristic type. Explain this postulate using modern genetic terms. Be sure to include the following terms in your explanation: dominant, recessive, allele, phenotype, genotype.
The continuity of life is based on heritable information in the form of DNA. Use the law of segregation and the law of independent assortment to explain how the passage of genes from parents to offspring (as alleles) ensures the perpetuation of parental traits in offspring and genetic variation among offspring. Describe briefly how Mendel demonstrated each of these laws.
Mendel's Laws of Inheritance Menders Success Menders approach to the study of heredity was effective for several reasons. Foremost was his choice of experimental subject, the pea plant Pisum sativum. Monohybrid Crosses Mendel began by studying monohybrid crosses— those between parents that differed in a single characteristic. The principle of segregation (Mendel's first law) states that each individual diploid organism possesses two alleles for any particular characteristic. These two alleles segregate (separate) when gametes are formed, and one allele goes into each gamete. Furthermore, the two alleles segregate into gametes in equal proportions.The concept of dominance that, when two different alleles are present in a genotype, only the trait of the dominant allele is observed in the phenotype. Multiple-Loci Crosses Dihybrid Crosses In addition to his work on monohybrid crosses, Mendel also crossed varieties of peas that differed in two characteristics (dihybrid crosses).…
Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. Would you decide to have a child if the test results said that you carry the mutation for breast and ovarian cancer? The heart disease mutation? The TSD mutation? The heart disease and the mutant alleles?
Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. Would you want to know the results of the cancer, heart disease, and TSD tests if you were Sarah and Adam? Is it their responsibility as potential parents to gather this type of information before they decide to have a child?
Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. If Sarah carries the mutant cancer allele and Adam carries the mutant heart disease allele, what is the chance that they would have a child who is free of both diseases? Are these good odds?