Match the following terms with their correct definition. A type of inheritance in which there is an earlier age of onset and a more severe phenotype in each successive generation. An effect in which the genotype of the mother determines the phenotype of the offspring. 1. Genetic anticipation 2. Position effect A type of inheritance were multiple genes contribute to the same phenotype. 3. Maternal effect 4. Pleiotropy A type of inheritance where one gene affects many different phenotypes. 5. Multigene (polygenic) inheritange An effect on gene expression from its location in an area of heterochromatin or euchromatin packaging.
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- In individuals affected by cystic fibrosis, salt crystals may appear afterperspiration dries up. In addition, the disease causes respiratory disorderswhich can be both debilitating and lethal. It occurs in individuals homozygousfor recessive gene. If 2 normal parents had a daughter with the symptoms ofthis disease, and a normal son, what is the probability that he might be acarrier of the recessive gene?Express answer in fraction form.AaBbCcDc AaBbCcD Ac Heading 1 Heading 2 Title Subtitle Subtle Em.. Emphasis Intense E... Strong Quote Int Paragraph Styles 4 Genetic Inheritance Patterns Retinitis pigmentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked. Apparently the dominant forms are often less severe. Eric's form of RP is Usher's Syndrome, which is an autosomal recessive inheritance (i.e., you must get a copy of the defective carried on one of the chromosomes that determines sex. Usher's Type II is recessive, so for Eric this means that both his Mom and Dad are carriers of this condition. His brother, Dirk, does not have any symptoms of RP. gene from your Mom and one from your Dad). Autosomal means it is not Question below short answer approach image you are the genetics counselor, should Eric have children? Imagine he has a daughter (he has two, but both are adopted). What advice would you give Eric if his wife was a carrier from a genetics counseling viewpoint? Describe all the possibilities,…Name: 2. Some ladybugs have 10 black spots on their shells and some have 4. When true breeding 10 spot individuals are crossed with true breeding 4 spot individuals, the offspring have 7 spots. a. Propose two distinct explanations for this finding. Explain the nature of spot inheritance in each case. D. rew bacteria erred them figure above would of14N7 then ely 2 moldon omrod abitqaq ratlsmmem sge of delw toiisoibom s s neu not oomod aid to soubnup ogusl onomod odi to slevel ismon oouborg o o consu ud od souboini bluow uoy dairlw yd za00oq sdi mialex b. Propose an experiment that would distinguish between these possibilities. sor proieins
- A 31 year old woman consults her physicain because she is concerned about developing breast cancer. She is currently in good health and she has never had any breast disease. Her concem arises bacause her sister has just been diagnosed as having breast cancer and her mother died of breast cancer. How can one determine if the cancer in this family is likely to be a dominantly inherited predisposition? b. What is the woman's cahnce of developing breast cancer? а.Pseudohypertrophic muscular dystrophy is an inheriteddisorder that causes gradual deterioration of the muscles. It isseen almost exclusively in boys born to apparently unaffectedparents and usually results in death in the early teens. Isthis disorder caused by a dominant or a recessive allele?Is its inheritance sex-linked or autosomal? How do youknow? Explain why this disorder is almost never seen in girls.Two mothers give birth to sons at the same time at a busy urbanhospital. The son of mother 1 has hemophilia, a disease causedby an X-linked recessive allele. Neither parent has the disease.Mother 2 has a son without hemophilia, despite the fact thatthe father has hemophilia. Several years later, couple 1 suesthe hospital, claiming that these two newborns were swappedin the nursery following their birth. As a genetic counselor, youare called to testify. What information can you provide the juryconcerning the allegation?
- Achondroplasia is a rare dominant autosomal defect resulting in dwarfism. The unaffected brother of an individual with achondroplasia is seeking counsel on the likelihood of his being a carrier of the mutant allele. What is the probability that the unaffected client is carrying the achondroplasia allele?If you knew that a devastating late-onset inherited disease runsin your family (in other words, a disease that does not appearuntil later in life) and you could be tested for it at the age of 20,would you want to know whether you are a carrier? Would youranswer be likely to change when you reach age 40?er What is the most likely mode of inheritance for this trait? I TO 2 2 3 8 9 10 1 DOD 1 2 3 OX-linked dominant OX-linked recessive O Y-linked O autosomal recessive O autosomal dominant IV 1 3 5 6 4 5 6
- Suppose a maternal effect gene exists as a functional dominantallele and a nonfunctional recessive allele that causes a disorder.A mother with the disorder produces offspring that are all withoutthe disorder. Explain the genotype of the mother.1. The pedigree chart in Figure 5.29 shows the inheritance of haemopiu family. Study the pattern of inheritance in the pedigree chart, and then answer the questions that follow. о 5 6. 3 8 9 10 11 Key Unaffected male Haemophiliac male О Unaffected female Fig. 5.29 Pedigree chart of a family affected by haemophilia a) What is the genotype and phenotype of individuals 2 and 4? b) (i) How many of the unaffected family members are definitely carriers of the recessive allele? (ii) How are you able to tell which of the family members are carriers? (4) (1) (3) c) (i) If Individual 11 marries a carrier female, what percentage of their sons is likely to be haemophiliacs? (1) (ii) Use a genetic diagram to show how you worked out your answer in i, (6) 2. Why is haemophilia never passed from father to son, even though it is most common in males? (4) 3. Can a mother pass on a sex-linked gene to her daughter? (1) 4. Sipho has red-green colour blindness. One of his grandfathers was also. colour…A recently married man and woman discover that eachhad an uncle with alkaptonuria (black urine disease), arare disease caused by an autosomal recessive allele of asingle gene. They are about to have their first baby. Whatis the probability that their child will have alkaptonuria?