Below is a table that lists the labeled autosomal genes for this female karyotype. Select the correct answer for the following GENOTYPE(s) and PHENOTYPE(s). NOTE: You must use the 'drop-down' for EACH question where it says "select". You may need to use the scroll bar to move left and right/up and down to view the full table. Genotype Phenotype [Select] [Select] MCR-1 ⇒ [Select] [Select] LDLR = [Select] [Select] ABO
Q: Dizygotic twins are no more or less genetically similar than are other pairs of ________________.
A: Twins are named so because some of their completely identical features but there are certain…
Q: What are the 5 spaces of the infrahyoid neck and the contents of each?
A: We know that The infrahyoid neck is the area of the neck between the hyoid bone and the thoracic…
Q: The physician’s order for Prinivil (lisinopril) is 20 mg p.o. BID for high blood pressure. The drug…
A: Introduction Prinivil:- It is a prescription medicine given by doctors which are used to treat the…
Q: Young children have "more" bones than adults. What happens to those "extra" bones?
A: Introduction Bones are composed of specialised bone cells and connective tissue that has been…
Q: What can be done at home to reduce the amount of bacteria on food?
A: Bacteria These are single-celled prokaryotic organisms that are present almost everywhere. Some…
Q: All organisms belonging to domains cells. bacteria and protista fungus and bacteria archaea and alga…
A: Prokaryotes are typically tiny, single-celled creatures with a simple structure. The majority of…
Q: What do you understand by “Sequencing by synthesis?” What is FRED score? Give an example.
A: DNA sequencing help in understanding basic structure of DNA which is nucleotide. Sequencing help us…
Q: Free energy (G) W+X Figure 6.2 с Select one: O a. A O b. Y+Z 0 c. c O d. B O e. W+X Direction of…
A: Enzymes are biocatalyst. Some enzymes are only made up of amino acids while others consists of…
Q: E. it can be used on hair and In anaerobic fermentation pyruvate is further oxidized to lactate or…
A: During aerobic respiration, by the process of glycolysis glucose molecule is broken down into form…
Q: Physician Edward H. Clarke published a treatise opposing higher education for women (Clarke, 1873).…
A: Dr. Edward H. Clarke's in 1873 had to face severe negative reactions from their opponents when he…
Q: If the resting membrane potential of a cell was +70 mV, the ELECTRICAL driving force on sodium would…
A: A neuron's purpose is to turn the message received from the external environment into an electrical…
Q: In detail explain how C3 plant leaf is different from C4 plant leaf and why
A: INTRODUCTION the difference between C3 and C4 plant leaves explained below.
Q: i have a gene (3222bp) i want to put it into a expression vector (pet 28b+),when i did pcr i flanked…
A: Introduction Gene cloning is the technique to produce the exact copies of the desired gene by…
Q: What are the key anatomical and physiological changes that occur in the renal system of an infant at…
A: Renal system It refers to the organ system that produces urine in the kidneys and transports it to…
Q: True or False: (T/F) Physical forces acting on the thorax and wing hinge during flight are detected…
A: Insects have flight muscles attached directly to their wings. Flight muscles move the wings…
Q: Using an online search, find if ultraviolet light can "kill" SARS-CoV-2. If so, which type(s) of UV…
A: Note:- Sorry, As per the honor code we aren't allowed to cite external references. Thank you!…
Q: Is the bacteria staphylococci harmful to humans?
A: Staphylococci can cause many forms of infection. (1) S aureus causes superficial skin lesions…
Q: The term, "cell" was coined by Andreas Vesalius Robert Hooke Antonie van Leeuwenhoek Rudolf Virchow
A: Cell is the basic building block of all the living organisms. It is the structural and functional…
Q: During staining, the first step is to dewax the slide. What is the purpose of the step? What is the…
A: Introduction :- In microscopy, staining is a technique used to increase contrast in a microscopic…
Q: If decomposers were removed from an ecosystem, which of the following scenarios below would occur 
A: Introduction An ecosystem is a region where a bubble of life is created by plants, animals, and…
Q: What is the typical composition of Harris Hematoxylin Solution? Which cellular organelle was more…
A: Typically employed at the microscopic level, staining is a method for enhancing contrast in…
Q: EXPLAIN HOW MITOCHONDRIA PARTICIPATED IN CELL DEATH??
A: Apoptosis is interceded by proteolytic enzymes called caspases, which trigger cell death by cleaving…
Q: Cell Structure and Function Match the following organelles to their descriptions 1. 2. 3. 4. 5. cell…
A: A cell is the basic structural and functional unit of living organism. Cell is the basic building…
Q: Q6.1: Under what metabolic conditions are excess carbohydrates be converted to stored…
A: When too much carbohydrate is taken, glucose is transformed into glycogen until the body's limited…
Q: In radish the effect of the alleles producing the red long variety is incompletely dominant over the…
A: Incomplete dominance is a gene interaction in both alleles expressed partially and one allele not…
Q: Upon observation of the nutrient agar slant culture, you strongly suspect that the culture is…
A: Microbes are microscopic organisms that cannot be seen as such through naked eyes. Special…
Q: a). define fitness in terms of an evolutionary term what does fitness mean? b). by what process…
A: Evolutionary biology is subfield of biology which studies the evolutionary processes that accelerate…
Q: What are the neurotransmitters that bind to ionotropic channels and allow for cation influx? Select…
A: The signalling process cannot operate without chemical messengers called neurotransmitters. They are…
Q: Why will a strict anaerobe grow in thioglycollate broth even when the medium is exposed to…
A: Introduction :- Anaerobic bacteria are microorganisms that can thrive without oxygen. For instance,…
Q: The difference between asexual and sexual reproduction is that O A. asexual reproduction occurs only…
A: The generation of descendants can be referred to as reproduction. Asexual reproduction is one of the…
Q: (T/F) Balance and body position during flight would be monitored in part using hair plates located…
A: Question 1: True In bee hair plates are located in neck, at petiole and the junction where leg meet…
Q: The following contains the same concentration of particles in comparison t another body of fluid: O…
A: Introduction: The overall solute concentration in a solution is referred to as osmolarity. There are…
Q: AX pro pro BX met met X arg arg DX Hfr
A: Conjugation: It can be described as a transfer mechanism in which the two bacterial cells come in…
Q: Explain the Methods and standards for disposal of biomedical waste
A: Any garbage that contains infectious (or possibly contagious) components is referred to as…
Q: What is the Posner task? Describe its purpose and setup (materials, conditions, etc.). What do its…
A: Posner task Michael Posner postulated this task. It refers to the neuropsychological test frequently…
Q: What is meant by the term biology
A: Introduction: The methodical study of the structure and behaviour of every natural and physical item…
Q: List and describe the stages of the cell cycle.
A: "Cell division" is a set of processes that occur in a cell leading to its maturation and eventual…
Q: What is the most likely mode of inheritance for the trait shown in the following pedigree? This…
A: This is an autosomal recessive trait.
Q: Outline the specific differences in the pelvis and the femur that are associated with bipedalism in…
A: Introduction :- When an organism uses its two back limbs or legs to travel on land, this is known as…
Q: Explain in details the evolution and orgin of toad, frog , salamander and cacelium also provide…
A: Ectothermic tetrapod animals of the group Amphibia are known as amphibians. The phylum Lissamphibia…
Q: What particular pathways or enzymes appear distinct for sulfate reducing bacteria in order to…
A: INTRODUCTION : Sulfate reducing bacteria - It is a type of bacteria which can reduce sulfate.They…
Q: How are food products altered for those who do not make adequate amounts of this enzyme
A: Enzymes are proteins that can speed up a reaction without being eaten because they are catalytic or…
Q: which are important for as cofactors in order to work. Dehydrogenases are examples of they often…
A: *Dehydrogenases are enzymes which mediate biochemical reactions by removing hydrogen atoms instead…
Q: Hos is the contractile vacuole different in appearance from the Amoeba
A: A contractile vacuole is a kind of vacuole that expands to gather water and its accompanying solutes…
Q: Fill-in the blank A person who is heterozygous for sickle-cell anemia a. has the disease b. C. does…
A: The recessive allele (written in small characters) is obscured in the presence of the dominant…
Q: Select the true statements: A.) It is possible, through genetic engineering, to fuse a fluorescent…
A: Explanation: -A fluorescent fusion protein can indeed be produced by fusing a fluorescent…
Q: 8. You have sequenced a segment of DNA from a species in the genus Lithobates (true frogs). The…
A: Template strand is a sense strand. and the coding stand which actually does not codes for m RNA is…
Q: How have humans manipulated each of these postulates in natural or artificial systems?
A: introduction : Darwin made contributions to the study of evolutionary biology as a naturalist. His…
Q: Which of the following is/are true about action potentials? Select all correct asnwers. Group of…
A: The rapid flowing of ions in neurons results in A sudden rise or fall in the membrane potential of…
Q: “How this picture demonstrates people helping to maintain biodiversity?” Are people planting one…
A: The variety of life forms including microbes, plants, and others that can be found in a given…
asap
Trending now
This is a popular solution!
Step by step
Solved in 2 steps
- Name Sofia Falcione P Pedigree Analysis Practice - for each pedigree, write the genotypes of the individuals The disorder shown on the pedigree is Maple Syrup Urine Disease (MSUD) which is a metabolic disorder that affects the body's ability to process certain proteins. It was named after a distinctive odor of a baby's urine. 1. What is the inheritance pattern of this gene? a) autosomal dominant b) autosomal recessive c) X-linked recessive 2. Provide at least one piece of evidence for your claim. This pedigree shows the inheritance Leber congenital amaurosis (LCA) which is a type of hereditary blindness. Individuals with this disease lose their vision during childhood. 3. What is the inheritance pattern shown? 4. Highlight one individual whose genotype is unknown. What additional information would you need to determine his/her genotype? Marfan syndrome affects the connective tissue and causes individuals to have long, thin, arms, legs, fingers and toes. 5. What is the inheritance…d/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? !!!KARYOTYPE #8 ZWK99032 KEY 14 15 17 19 21 22 Y Is this karyotype male or female? What kind of error (if any). Name of syndrome 9. 3. 20 OXEO gerte
- /d/1n5NtidRwTwUzcDkDPi5Z9P_SHPZ91A-XH-pfftLbhNc/edit (1) O pols Add-ons Help Last edit was seconds ago BIUA ミ: 12 + ext Calibri I|1 6 I 2 Section 5: Trihybrid cross and Laws of probability For a trihybrid cross, in which inheritance of alleles for three genes is tracked, drawing a Punnett square that combines all three genes may not be practical. Instead the laws of probability may be used. The product law of probabilities says that when alleles for separate genes segregate independently, we can figure out the probability of a particular combined genotype by multiplying the probability of the alleles for each gene. 13. We cross a homozygous tall pea plant with yellow, round seeds to a homozygous dwarf pea plant with green, wrinkled seeds. All the F1 offspring are all tall plants with yellow, round seeds. a. What are the expected F2 ratios (use fractions) of tall and dwarf plants? b. What are the expected F2 ratios (use fractions) of yellow and green seeds? C. What are the expected F2…patibility Mode] UE Layout References Mailings Review View A A Aa vA 前、一间刷 一| T AaBbCcDdE AaBE x A Av X, Normal No Spacing Headi co Edit and Save Start your free one month trial of Microsoft 365 or sign in to activate an existing subscription. 9. In human beings, the gene for red-green colorblindness (r) is sex-linked and recessive to its allele for normal vision (R), while the gene for freckles (F) is autosomal and dominant over its allele for nonfreckled (f). A nonfreckled, normal-visioned woman whose father was freckled and colorblind, marries a freckled, colorblind man whose mother was nonfreckled. a. What is the genotype of the woman's father? b. What is the probability that the couple's first child will be a non-freckled, normal visioned girl c. What is the probability that the first two children born to the couple will be freckled and colorblind girls? d. What is the probability that the first child born to the couple will either be a freckled, colorblind boy or a non-freckled,…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?Use keyboard only to enter your answer below. ALL WORKING MUST BE SHOWN Problem 1) mutation in a gene on chromosome 15 that codes for an enzyme. The disease is an inherited autosomal recessive condition which is Tay-Sachs disease is caused by loss of function found amongst Ashkenazi Jews of Central European origin. In this population, 3 in 5,200 children are born with the disease. What proportion of the population are carriers (heterozygotes) for this disease?
- 40 Below is a pedigree of a family, some of whom have the autosomal dominant condition Huntington's disease. Affected individuals are indicated by a dark square or circle. The male in generation I (indicated by the arrow) is heterozygous for the Huntington's disease mutation. The following two questions relate to this pedigree. Generation II II If H represents the disease allele, and h the wild type allele, what is the genotype of the individual indicated by the *? Select one alternative: O hh O Hh O hH O HHtion 8: below is the pedigree of inheritance of phenylketonuria (PKU). We will designate the letter Caven for the dominant allele and "p" for the recessive allele. 4 The pedigree shows that the pattern of inheritance for the allele for phenylk ylketonuria is: I. II. 1 III. IV. Autosomal dominant Autosomal recessive X-linked dominant X-linked recessive b. The parents in generation I have how many children: I. 3 Boys II. 3 Girls III. IV. 3 Boys and 1 Girl 3 Girls and 1 Boy c. What is the genotype of individual 1 in generation III: I. PP II. pp III. Pp " O 1 III. 50% E III 1 ▬ 2 2 IV. 25% 1 3 IV. Can be PP or Pp ii. Suppose that a man having type AB blood marries a woman having type O blood. What is the probability that their child will have type A blood? I. 100% II. 75% 2 4 35 & :56M ******* 24 DIHYBRID CROSSES DRV 0 Stv T alı A @ zladenA 9160p2-id2 bns obidalbaneoviene da II\ MOD YR 21 $59A ... Create a dihybrid cross and determine the expected phenotypic percentages of the offspring of two corn plants both of which are heterozygous for colour and texture (RrTt X RrTt). Don't forget to include clear let statements, and follow the all six steps taught on solving genetics problems. insig moni nellog: bna. zoom