a. b. C. Pedigree of a Family with Cystic Fibrosis d. I 1 2 3 4 Note: Cystic fibrosis in this family is caused by a recessive allele that is found on chromosome 7. A genetic counsellor collected pedigree information regarding the incidence of cyctic fibrosis within this family. The row that indicates the genotypes of individuals 1-1, 1-2, and II-2 is Select one: II I-1 XAY I-1 AA I-1 XAY 1 I-1 Aa 1-2 хаха 1-2 aa 1-2 ΧΑΧΑ 2 1-2 Aa II-2 XAY 11-2 Aa II-2 xay 11-2 aa O
Q: 1. Where can we find the Circle of Willis in 10 mm pig embryo? What are the branches associated with…
A: The study of an organism's body's structure is known as anatomy. It is the area of biology that is…
Q: How is complementation a useful technique in understanding allelism and gene function
A: When two varieties of an entity have separate homozygous recessive mutations, if they both display…
Q: How is telomerases related to ageing? How Can telomerase- related ageing be addressed…
A: Humans lose physiological and psychological function as they age, which is a normal process. The…
Q: Examine whether the statement "every tissue that can be renewed from a tissue-specific population of…
A: Undifferentiated cells called stem cells have the propensity to specialize into several cell types.…
Q: Actin in action, muscle satisfaction. The movement of biceps require sarcomere _______. Select one:…
A: If the muscle cells are examined under a microscope, a striping design can be seen, these structures…
Q: True or false The conversion of pyruvate to acetyl coa requires energy input into the format of…
A: The conversion of pyruvate to acetyl coa takes place for acetly coa to join aerobic respiration.…
Q: ANATOMY question (not a medical school course) “Ron (he/his) is a 60-year-old man is experiencing…
A: Rotator cuff tear Four muscles and tendons that stabilize your shoulder joint and allow you to lift…
Q: Briefly explain why DNA replication is an exergonic process
A: Genes are the hereditary unit that are exhibited on the long thread like structure that are…
Q: Oils, such as vitamin E acetate, are sometimes added to vaping products. How do these oil additives…
A: Issues for the impacts of vaping on our lives have been steadily increasing over the last…
Q: In lecture, discussed was a study by Pang Wen et al, titled "Minimum amount of physical activity for…
A: The study examined the health advantages connected to a variety of physical activity levels in…
Q: Which of the following statements is FALSE regarding a rightward shift in the hemoglobin-oxygen…
A: The oxygen–hemoglobin dissociation curve, also known as the oxyhemoglobin dissociation curve or…
Q: Distilled water Red onion cell-swelis up
A: In this picture Osmosis is shown. Osmosis is a kind of movement of solvent molecules( here in this…
Q: Does paracemol have risks of hepatic toxicity Give in regards to a pateint.
A: Paracetamol is a drug of NSAIDs category . it is also known as acetaminophen. it use as Antipyretic…
Q: Which of these observations provides evidence that we have several types of taste receptor? A.…
A: Sweet foods have always appealed to humans. Humans have loved nutritive sweeteners such as honey and…
Q: 1. Use the prokaryotic gene DNA sequence below to answer the following questions: 1 11 21 31…
A: The DNA sequence is replicated to produce daughter DNA which is the same as the parent DNA. Further,…
Q: During apoptosis, rates of protein degradation activity. Select one: a. decrease, decrease b.…
A: Apoptosis is a process of cell death that is mediated by proteases. Proteases are enzymes that…
Q: nes at QRT gene in one pair of wins, And and Becca, at 1 year of age, again when they are 25 years…
A: The sequences in the DNA determine the phenotype of an organism. But not all sequences in a DNA are…
Q: 6) What does it mean to say that mosses and other nonvascular plants have life cycles dominated by…
A: The non vascular plants like mosses which come under bryophytes do not have vascular tissue xylem…
Q: In flies, long wings (W) are dominant to short wings (w). Two homozygous recessive flies are…
A: Homozygous recessive means that the organisms has birth the copies of the same allele that will not…
Q: Tiffany suffers from primary narcolepsy. Occasionally, during the day she experiences total loss of…
A: Narcolepsy refers to a sleep disorder that is characterized by various symptoms. Lack of the brain…
Q: The Bax protein, thus Select one: apoptosis. a. none of the above b. inhibits caspase activity,…
A: Introduction : All multicellular organisms, including plants and animals, go through the…
Q: xplain the way in which change in the state of differentiation of Acute Promyelocytic Leukemia (APL)…
A: Introduction: White blood cells can develop a malignancy known as acute promyelocyte leukemia (APL…
Q: Both intermediate filaments and microtubules can be found in the nucleus. Select one: a. False b.…
A: INTERMEDIATE FILAMENT They are cytoskeletal structural components found in the cells of both…
Q: In the experiments below, different prokaryotic cells were grown in broth cultures in the presence…
A: Antibiotic resistance arises when changes in bacteria make antibiotics less effective in treating…
Q: The client for whom you are caring had the following for breakfast: 4 fluid ounces of milk, 6 fluid…
A: Our body has a large fluid requirement. The fluid is taken in various forms and it must be taken in…
Q: How does Carbon Capture, Usage and Storage(CCUS or Carbon capture and storage(CCS) affect…
A: chemoautotrophic process found in bacteria and alage. this process help to make their own food by…
Q: Assume that you know RNA polymerase will move to the right during transcription. On the diagram…
A: Transcription is a heterocatalytic action of DNA by means of which RNA is synthesized from specific…
Q: B complex vitamins major function is to_____ Group of answer choices All of the above Act as…
A: People require trace amounts of organic substances called vitamins. The body either cannot make…
Q: For the cell cycle to progress normally, the protein by Select one: a. cdk, a protease b. cyclin,…
A: Introduction Cell cycle consists of series of events that help in the cell division. It is divided…
Q: Select the statement that is correct about why physicians cannot harvest the organs from…
A: A baby who is born without some of their brain has a serious birth abnormality called anencephaly.…
Q: Explain your answer in some depth and avoid just saying "It is A" or It is B. Defend your answer and…
A: Different species concepts try to define species on the basis of certain characteristics. The major…
Q: Step #1 Culture and perform a Gram-stain on the Super Bug You culture the Super Bug by swabbing the…
A: Bacteria are simple unicellular prokaryotic microorganisms that lack membrane bound organelles and…
Q: The “rest and digest” portion of the autonomic nervous system is also called the Question 4…
A: The paraventricular nucleus is the primary hypothalamic region for the central regulation of the…
Q: The absence of p53 ____ the cell cycle. The absence of retinoblastoma ____ the cell cycle. Select…
A: A cell's growth and division are accompanied by a sequence of processes known as a cell cycle. A…
Q: romosomes and Heredity tiple Choice: Write the CAPITAL letter of your answer choice in the blank AND…
A: 1) A family chart, diagram or record or a history which indicates or determines the individual in…
Q: Which of the following is part of the hindbrain Question 9 options: A) Pons B) Tectum…
A: The swollen part of the central nervous system located in brain box, having cavities filled with…
Q: According to U.S. law, after a certain number of years experimental chimpanzees should: Be sent to a…
A: According to U.S law, after a certain number of years experimental chimpanzees should be sent to…
Q: a) Draw a phylogenetic tree based on characters 1-5 in the table below. Place hatch marks on the…
A: This phylogenetic tree is a hypothesis because they reflect the best model, or explanation, of…
Q: Draw a diagram of Hydrogen gas being produced by water electrolysis to enhance the biogas produced…
A: Biofuels represent the renewable source of energy. They help in the production of ethanol and…
Q: Explain the following briefly. 1. Describe the characteristics of sound that are perceived by…
A: Introduction The body's organ, which helps to maintain the hearing and body balance, is called the…
Q: Which of the following proteins would least likely promote arrest of cell division or apoptosis?…
A: Apoptosis: a kind of cell death where a cell dies as a result of several molecular events. One way…
Q: Cleavage divides the eggs of vertebrates and many other animals into a cluster of separate cells. By…
A: An embryo in development is an excellent example of intricate biological self-organization and…
Q: Glycogenolysis, reaction scheme and regulatory enzymes.
A: Together with glycolysis, glycogenolysis is essential for the metabolism of carbohydrates. It is the…
Q: Explain the mapping of odours inside the olfactory epithelium, olfactory cortex, and the olfactory…
A: A. OLFACTORY RECEPTORS 1. The sense of smell arises from stimulation of receptors in the yellowish…
Q: Prader-Willi Syndrome (PWS) is caused by a mutation in an autosomal gene that is maternally…
A: Given information Prader-Willi Syndrome occurs by the mutated autosomal gene that is maternally…
Q: 1.Begin in the blood vessel entering the kidney (renal artery), trace a molecule of water as it…
A: Urinary system: The kidneys, ureters, bladder, and urethra make up the urinary system, commonly…
Q: As an epidemiologist you are going to investigate the effect of lead exposure in a Baltimore…
A: The number of new incidents or instances of illness divided by the total number of people in the…
Q: Does consuming too much water create hypertonic, hypotonic or isotonic environment in the body fluid…
A: Water, inorganic salts, and organic substances make up cells. Water makes up the majority of…
Q: In shorthorn cattle, a roan cow mated with a roan bull always produces red, white, and roan claves…
A: According to the Q&A guidelines, we are supposed to answer only three sub-parts. Kindly repost…
Q: What are decentralised biofuel plants?
A: Introduction Biofuel is any kind of fuel that is directly derived from plant or animal matter, also…
Trending now
This is a popular solution!
Step by step
Solved in 3 steps with 1 images
- Pedigree 2: A. What is the most likely mode of inheritance of this disease? Choose from: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive. B State the genotypes of individuals # 1 #4. C If individual #3 has another daughter with the same partner, what is the probability that this daughter will be affected (show the disease)?I. Give the chromosome number and chromosome configuration if the following mutations occurred in rice, a diploid organism wherein the number of chromosomes per set is 12. 1. Trisomy-11 2. Double Monosomy 3. Triploidy 4. Nullisomy-12 5. Tetraploid II. Give the chromosome number for the following: 6. 311+ 21 7. 4||+3||| 8. 2n=4 treated with colchicine to produce an autotetraploid 9. Monoploid maize (2n=20) 10, 51|^+ 51|Bа. What type of inheritance is shown in the pedigree? II 2 II 1 2 4 IV Identify the genotypes of the following individuals: III- 2 b. |-1 Il- 2 III-4 IV-1 + v Paragraph В I
- BB AB AB A. None B.3 с.1 D.2 ВВ OE. The father AB In the pedigree presented above, an autosomal dominant disease which causes significant visual loss and eventual blindness, is segregating in the family. The disease gene causing this sight loss looks as if it may be linked to a marker locus. The alleles of this marker locus that are present in this family are allele A and allele B. Are there any recombinant individuals in this pedigree? AB ВВ AB ВВ AB ВВ AB AB ВВ27 What is the most probable mode of inheritance for the genetic disorder shown in this pedigree? KEY Affected Affected Unaffected Unaffected Male Female Male Female Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. autosomal recessive b autosomal dominant X linked27 What is the most probable mode of inheritance for the genetic disorder shown in this pedigree? KEY Unaffected Male Unaffected Female Affected Affected Male Female Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a autosomal recessive autosomal dominant X linked
- 25 What is the most likely mode of inheritance for the attached pedigree? Female Affected Male Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a Autosomal recessive b Autosomal dominant X-linkedIdentify the type of chromosomal aberration described in each of the following cases: a. loss of a chromosome segment b. extra copies of a chromosome segment c. reversal in the order of a chromosome segment d. movement of a chromosome segment to another, nonhomologous chromosomeA 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?Describe the chromosomal alterations and phenotype of cri du chat syndrome and Prader-Willi syndrome.