Q: You are investigating a new kind of flatworm and give it food attached to charcoal pieces so that…
A: The objective of the question is to identify the type of digestive system in a flatworm based on the…
Q: The Casparian strip prevents apoplastic movement through the epidermal cells of the stem. True or…
A: The objective of the question is to determine whether the Casparian strip prevents apoplastic…
Q: Why is cultural competency one of the essential skills for a cancer program planner?
A: The objective of the question is to understand the importance of cultural competency in the role of…
Q: What kind of biological molecule is this?
A: Living organisms are made up of cells which are further made up of different biomolecules. Usually…
Q: Which of the following statements characterize the megaphyll line of evolution? A) They differ from…
A: The objective of the question is to identify the correct statement(s) that characterize the…
Q: Female gametophytes develop specifically within what part of the pine cone? -Pollen sac -Anther…
A: The objective of the question is to identify the specific part of the pine cone where female…
Q: Which RNA polymerase is responsible for transcribing protein coding genes? Group of answer choices…
A: RNA polymerase transcribes RNA by moving along a DNA strand. During the transcription process, an…
Q: 3). The diagram below shows growth of E. coli strains 1 through 4 on a variety of media. Small dots…
A: Auxotrophy is the inability of an organism to synthesize a particular biochemical compound required…
Q: According to the information in the lab manual, lampreys do not have a stomach or a distinct…
A: Lampreys are cartilaginous fish , they are jawless ( Agnatha). Its mouth has distinct circular disc…
Q: During bacterial replication, concurrent synthesis is assisted by the specific action of gyrase ODNA…
A: Concurrent DNA synthesis means that both the strands unwind at the same time and DNA replication…
Q: Which ones fit into the categories?
A: Cells can be divided on the basis of the presence of certain organelles into prokaryotic and…
Q: Please demonstrate the genotype, DNA synthesis, and Prophase 1 of the diploid organism going through…
A: Meiosis is a sort of cell division that results in four daughter cells each with half the number of…
Q: When Talia’s daughter isn’t feeling well before school, she gives her a spoon of honey that looks…
A: Delusional thinking is a phenomenon in which a person has particular views about something that are…
Q: Describe the process to get a specimen into view using the 40X objective starting from the point…
A: ExplanationThe first step is to place your slide on the microscope stage. Make sure the specimen on…
Q: Consider a corn plant whose genotype for the traits of kernel color, kernel texture, and stem height…
A: The objective of this question is to determine the number of unique gametes that can be produced by…
Q: The production of root hairs identifies which zone in the root -the zone of cell division -the…
A: The objective of the question is to identify the zone in the root where the production of root hairs…
Q: For a medical scaffold surgically implant around the body of the pancreas, explain which areas on…
A: The pancreas organ found within the abdomen, encompassed by a few other organs and major blood…
Q: Match the organisms or structure to the type of scope you would use to FIRST start investigating its…
A: A compound microscope is utilized for viewing samples at high magnification (40 - 1000x), which is…
Q: an independent variable is the variable measured in an experiment. True or False
A: People who want to learn more about the natural world engage in science. It is frequently carried…
Q: How would lack of health literacy impact the patients and a cancer program’s activities?
A: The objective of the question is to understand the impact of lack of health literacy on patients and…
Q: pe
A: We must first determine the compound's molar mass to compute the mass.Carbon(C) = 2O * 12.011 g/mol=…
Q: List the parts of the ear and the eye, and briefly describe the function of each structure.
A: Eye and ear are the photochemical and hearing organs respectively. These are further divided to…
Q: 1. 2. 3. 4. 5.
A: Each part of a plant serves a specific purpose in its growth and development.1) Flower: The primary…
Q: Describe the process for identifying a cancer program’s adjustment needs
A: The objective of this question is to understand the process of identifying the adjustment needs of a…
Q: 1). A cis test of two T4 rll mutants yields 1000 plaques on E. coli B and 10 plaques on E. coli K12.…
A: B.Yes, the rule of two should be used here. The rule of two is a statistical method used to ensure…
Q: Consider the following statement. Is it true or false? Why? Please justify your answer explaining…
A: The process of development by gradual changes that is the change in characteristics of a species…
Q: Oxycodone has a high affinity for the mu receptor, and when it binds to this receptor, it produces a…
A: Oxycodone is a type of opioid drug used to relieve pain. Like any other opioid drug it may bind to…
Q: The protrusible rasping organ in a mollusk's mouth that is used to scrape food from the substrate is…
A: The question is asking about the specific organ in a mollusk's mouth that is used for feeding.…
Q: Tandem duplication of a gene may be a result of deletions. . a recombination error. gene conversion…
A: The structural rearrangement of a part of DNA either by its duplication or insertion of a segment of…
Q: = Chapter 11- Hormones ▬▬▬▬▬▬▬ 10 IN 20 [ 16 14 Across Down in the blood 2. Which hormones…
A: The chemical substances which act like messengers in our body are known as hormone. They made in one…
Q: Use the following diagram of the male reproductive system to answer Questions A B C D- E- -F G H 14.…
A: The parts of the Male reproductive organs:Pen*sTestesScrotumEpididymis UrethraSeminal VesicleVas…
Q: I have a culture containing 106 organisms/ml and need to dilute it to 1000 organisms/ ml. Can…
A: Serial dilution is procedure by which a stock solution containing a high concentration of…
Q: Which two social justice principles does a health program consider, and why does it consider them?
A: The objective of the question is to identify two social justice principles that a health program…
Q: Differentiate between surface immobilisation and microencapsulation of enzymes and discuss the…
A: Surface Immobilization - It involves the immobilizing the enzymes by attaching enzymes to a solid…
Q: Energy from the sun is directly harnessed by _________ A.) producers B.)all organisms C.)consumers…
A: Ecology is a branch of science which deals with the study of the relationships between living…
Q: Consider the same graph shown. The right error bar is a measure of: Please choose the best option.…
A: To determine the correct answer, we need to understand what an error bar represents on a graph.In…
Q: 4) You design Drosophila crosses to provide recombination data for gene (A), which is located…
A: The location of genes on a particular chromosome can be determined on the basis of recombination…
Q: Cytosine makes up 15% of the nucleotides in a sample of DNA from an organism. Approximately what…
A: DNA is made up of nucleotides. Each nucleotide is made up of a phosphate group, deoxyribose sugar…
Q: field of view under the 100X
A: View diameter:This is a key concept in microscopy that encompasses the observable area within the…
Q: Match the type of enzyme inhibition on the left with the example of an inhibitor on the right. i…
A: 1. Competitive inhibition: - Example: Sulfa drugs2. Non-competitive inhibition by regulatory…
Q: About 13 servings per container Serving size ½ cup mix (54g) makes 3 pancakes As prepared Calories…
A: Nutrient Levels According to Label Terms:High:Based on the provided information, no nutrients…
Q: What is the field of view under the 100X objective of the microscope used in the previous question?…
A: In this initial phase, our goal is to understand and evaluate the provided formula designed to…
Q: Which levels of protein structure are determined by primary structure mark all that apply 1.…
A: Proteins are dynamic structures, and their conformational changes are often crucial for their…
Q: Alexander Fleming was working with bacteria called staphylococcus, which looked like bunches of…
A: Antibiotics were discovered by Sir Alexander Fleming by accident. While growing Staphylococcus, he…
Q: ✓ A chemist adds 240.0 mL of a 0.0058M calcium sulfate (CaSO4) solution to a reaction flask.…
A: The mass of calcium sulfate supplied to the flask can be calculated as follows:To calculate the mass…
Q: which biome is the hottest and coldest and wettest to driest in a diagram form. title, components…
A: A biome is different form an ecosystem; an ecosystem is the interaction of biotic and abiotic…
Q: Temperature is a measure of 1. Group of answer choices 2. How big molecules are 3. How fast…
A: The correct answer to what temperature is a measure of is:3. How fast molecules are moving.Here's…
Q: Where would one find the axillary buds in the plant stem? -between the leaf petiole and the leaf…
A: The objective of the question is to identify the location of axillary buds in the plant stem.
Q: Consider the trait in Figure 22.5a. Which statement about this trait is correct? Please choose the…
A: Evolution is the developmental process in which useful variations accumulate in a population and are…
Q: In order to allow the diffusion of islet beta cells encapsulated within the medical scaffold into…
A:
Genetics Question 6
Trending now
This is a popular solution!
Step by step
Solved in 4 steps
- Alberta is phenotypically normal, but her brother (Rodrigo) has albinism, which is caused by an autosomal recessive mutation. The probability that Alberta is a carrier (i.e., heterozygous for albinism) is [express your answer as a fraction]A couple was referred for genetic counseling because they wanted to know the chances of having a child with dwarfism. Both the man and the woman had achondroplasia (MIM 100800), the most common form of short-limbed dwarfism. The couple knew that this condition is inherited as an autosomal dominant trait, but they were unsure what kind of physical manifestations a child would have if it inherited both mutant alleles. They were each heterozygous for the FGFR3 (MIM 134934) allele that causes achondroplasia. Normally, the protein encoded by this gene interacts with growth factors outside the cell and receives signals that control growth and development. In achrodroplasia, a mutation alters the activity of the receptor, resulting in a characteristic form of dwarfism. Because both the normal and mutant forms of the FGFR3 protein act before birth, no treatment for achrondroplasia is available. The parents each carry one normal allele and one mutant allele of FGRF3, and they wanted information on their chances of having a homozygous child. The counsellor briefly reviewed the phenotypic features of individuals with achondroplasia. These include facial features (large head with prominent forehead; small, flat nasal bridge; and prominent jaw), very short stature, and shortening of the arms and legs. Physical examination and skeletal X-ray films are used to diagnose this condition. Final adult height is approximately 4 feet. Because achondroplasia is an autosomal dominant condition, a heterozygote has a 1-in-2, or 50%, chance of passing this trait to his or her offspring. However, about 75% of those with achondroplasia have parents of average size who do not carry the mutant allele. In these cases, achondroplasia is due to a new mutation. In the couple being counseled, each individual is heterozygous, and they are at risk for having a homozygous child with two copies of the mutated gene. Infants with homozygous achondroplasia are either stillborn or die shortly after birth. The counselor recommended prenatal diagnosis via ultrasounds at various stages of development. In addition, a DNA test is available to detect the homozygous condition prenatally. What if the couple wanted prenatal testing so that a normal fetus could be aborted?A couple was referred for genetic counseling because they wanted to know the chances of having a child with dwarfism. Both the man and the woman had achondroplasia (MIM 100800), the most common form of short-limbed dwarfism. The couple knew that this condition is inherited as an autosomal dominant trait, but they were unsure what kind of physical manifestations a child would have if it inherited both mutant alleles. They were each heterozygous for the FGFR3 (MIM 134934) allele that causes achondroplasia. Normally, the protein encoded by this gene interacts with growth factors outside the cell and receives signals that control growth and development. In achrodroplasia, a mutation alters the activity of the receptor, resulting in a characteristic form of dwarfism. Because both the normal and mutant forms of the FGFR3 protein act before birth, no treatment for achrondroplasia is available. The parents each carry one normal allele and one mutant allele of FGRF3, and they wanted information on their chances of having a homozygous child. The counsellor briefly reviewed the phenotypic features of individuals with achondroplasia. These include facial features (large head with prominent forehead; small, flat nasal bridge; and prominent jaw), very short stature, and shortening of the arms and legs. Physical examination and skeletal X-ray films are used to diagnose this condition. Final adult height is approximately 4 feet. Because achondroplasia is an autosomal dominant condition, a heterozygote has a 1-in-2, or 50%, chance of passing this trait to his or her offspring. However, about 75% of those with achondroplasia have parents of average size who do not carry the mutant allele. In these cases, achondroplasia is due to a new mutation. In the couple being counseled, each individual is heterozygous, and they are at risk for having a homozygous child with two copies of the mutated gene. Infants with homozygous achondroplasia are either stillborn or die shortly after birth. The counselor recommended prenatal diagnosis via ultrasounds at various stages of development. In addition, a DNA test is available to detect the homozygous condition prenatally. What is the chance that this couple will have a child with two copies of the dominant mutant gene? What is the chance that the child will have normal height?
- A couple was referred for genetic counseling because they wanted to know the chances of having a child with dwarfism. Both the man and the woman had achondroplasia (MIM 100800), the most common form of short-limbed dwarfism. The couple knew that this condition is inherited as an autosomal dominant trait, but they were unsure what kind of physical manifestations a child would have if it inherited both mutant alleles. They were each heterozygous for the FGFR3 (MIM 134934) allele that causes achondroplasia. Normally, the protein encoded by this gene interacts with growth factors outside the cell and receives signals that control growth and development. In achrodroplasia, a mutation alters the activity of the receptor, resulting in a characteristic form of dwarfism. Because both the normal and mutant forms of the FGFR3 protein act before birth, no treatment for achrondroplasia is available. The parents each carry one normal allele and one mutant allele of FGRF3, and they wanted information on their chances of having a homozygous child. The counsellor briefly reviewed the phenotypic features of individuals with achondroplasia. These include facial features (large head with prominent forehead; small, flat nasal bridge; and prominent jaw), very short stature, and shortening of the arms and legs. Physical examination and skeletal X-ray films are used to diagnose this condition. Final adult height is approximately 4 feet. Because achondroplasia is an autosomal dominant condition, a heterozygote has a 1-in-2, or 50%, chance of passing this trait to his or her offspring. However, about 75% of those with achondroplasia have parents of average size who do not carry the mutant allele. In these cases, achondroplasia is due to a new mutation. In the couple being counseled, each individual is heterozygous, and they are at risk for having a homozygous child with two copies of the mutated gene. Infants with homozygous achondroplasia are either stillborn or die shortly after birth. The counselor recommended prenatal diagnosis via ultrasounds at various stages of development. In addition, a DNA test is available to detect the homozygous condition prenatally. Should the parents be concerned about the heterozygous condition as well as the homozygous mutant condition?Mr. Steve W. genetics question Albinism is a recessive autosomal trait for skin pigmentation. Hemophilia is a sex-linked recessive disorder of the blood. assign alleles to the traits A – normal skin pigmentation XH – normal blood a – albino Xh - hemophilia A double heterozygous woman marries a non-hemophilic man and is heterozygous for skin pigmentation. Double heterozygous means heterozygous for both traits. Aa for skin pigmentation and XHXh for blood traits. Therefore, the genotype of the woman is AaXHXh. Non-hemophilic man is XHY and heterozygous for skin pigmentation is Aa. The genotype, therefore, of the man is AaXHY. What is the probability that they will have: a child with normal skin? _____________________ a child with normal blood? _____________________ an albino girl? _____________________ A hemophilic boy? _____________________QUESTION 8 Consider the following pedigree. With no other information provided, what is the most likely mode of transmission (or mode of inheritance) of the allele for the unusual trait? sex-linked recessive autosomal recessive autosomal dominant sex-linked dominant
- QUESTION 22 Consider whether the mode of inheritance for each of the pedigrees below is autosomal dominant or autosomal recessive Pedigree I Both pedigrees show autosomal dominant modes of inheritance Pedigree I is autosomal dominant while pedigree II is autosomal recessive O Pedigree I is autosomal recessive while pedigree II is autosomal dominant O Both pedigrees show autosomal recessive modes of inheritance QUESTION 23 A Pedigree II The pedigree below shows the inheritance of an X-linked recessive disorder. B TH Quersd/1n5NtidRwTwUzcDkDPi5Z9P SHPZ9IA-XH-pfftLbhNc/edit 1) @ Is Add-ons Help Last edit was 15 minutes ago | Calibri в I UA 12 + 3I | II 6 1 I 7. Construct a Punnett square for a cross between two heterozygous pea plants with violet flower color. a. What genotypes would you expect in the offspring? b. What percentage or ratio of each genotype would you expect in the offspring? !!!QUESTION 10 Consider the following pedigree. With no other information provided, what is the most likely mode of transmission (or mode of inheritance) of the allele for the unusual trait? autosomal dominant sex-linked recessive autosomal recessive O sex-linked dominant
- Tell me whether it is autosomal reccessive inheritance,autosomal domiant inheritance,sex-linked reccessive inheritance, sex-linked dominay inheritance or y-linked inheritance based on information given.(With Pedigree Anlaysis Breakdown)FAlpQLSfiOhfAvlhxzCSiUll_6rt-nU5b0WI73UmWOxkOw8OCwk01ng/formResponse B 1 2 Bb x Bb b 4 The fur in both parents in this cross is * 1 B B Bb x Bb b 3 4 brown black O homozygous dominant homozygous recessive 3. 近8:38 4 CamScanner 05-22-2022 20.38 Identify the follow pedigrees as autosomal or sex-linked AND whether they are dominant or recessive. No Shadow Original O Left Markup Lighten To Text JA Magic Color Signature B&W