Which of the following traits/disorders is controlled by multiple genes? Group of answer choices Tay- Sachs disease skin color ABO blood type curly hair familial hypercholesterolemia
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- Which of the following genetic disorders is described by the following: Recessive sex-linked disorder. More common in males. Results in the inability to distinguish some colors. Male-pattern baldness Cystic fibrosis albinism colorblindnessPlease fill in the following red areas.A couple has had a child born with neurofibromatosis. They come to your genetic counseling office for help. After taking an extensive family history, you determine that there is no history of this disease on either side of the family. The couple wants to have another child and wants to be advised about the risks of that child having neurofibromatosis. What advice do you give them?
- The geno. pe/s of people with freckles is/are: The genotype/s of people without freckles is/are:_ O Freckles: FF; No freckles: Ff, ff O Freckles: FF. Ff; No freckles: ff O Freckles: FF ff: No freckles: Ff O Freckles, f No freckles: FF, FfAaBbCcDc 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,…Cystic fibrosis is determined by simple dominant-recessive inheritance, where the trait for cystic fibrosis is recessive. Given Rnormal, r is CF gene, complete the following Punnett square
- Genetic disorders Complete the following statements to describe several genetic disorders and their symptoms. Choices can be used more than once. The disorder called causes blue-colored skin, sickle-cell disease osteogenesis imperfecta The disorder called that leads to weakened, brittle bones. causes defective collagen methemoglobinemia autosomal dominant The disorder called causes abnormally thick mucus in the bronchial tubes and pancreatic ducts. autosomal recessive The disorder called leads to progressive cystic fibrosis degeneration of neurons in the brain. alkaptonuria The disorder called causes urine to be black. Huntington disease acer %23 24 & 4 8. 9. e y u < 6Hemophilia is inherited as a sex-linked recessive trait. A non-hemophilic man marries a non-hemophilic woman whose father had hemophilia. With respect to this information, indicate all possible genotypes their children could possibly have. Show ALL work using punnett squares.Please select all of the following that are x- linked disorders. O Cystic Fibrosis red-green color blindness O Hemophilia Duchenne Muscular Dystrophy O Down Syndrome
- Normal No Spac Hemophilia is a blood clotting disorder that almost exclusively affects males. It is a sex-linked, recessive disorder (X). Using the details below, fill in the Punnett square to determine the percent probability of the couple having a child with hemophilia. Mother Father -carrier of -does not have hemophilia hemophilia -genotype XHX -genotype XY Mother. XH. Xh Father Probability of offspring having hemophilia: OFocusWhich of the options below is not an example of Pleiotropy? Tay-Sachs Disease phenylketonuria Marfan syndromeThere's more than one correct answers
