ANSWER
(E) 50%
Because a person affected by an autosomal dominant disorder has 50% chance of passing the mutated gene to each child.The chance that a chid will not inherit the mutated gene is also 50% However ,in some cases an autosomal dominant disorder result from a new mutation that occurs during the formation of egg or sperm cells or early in embryonic development. In these cases, the childs parents are unaffected ,but the child may pass on the condition to his or her own children.
Most frequent instance: Aa x AA ( marriage of an affected individual HEZ with a normal individual).
Question 25 4 points Save This pedigree (Pedigree #2) illustrates the inheritance of a simple Mendelian...
This pedigree (Pedigree #1) illustrates the inheritance of a simple Mendelian disorder. Individual 1 marries and decides to have children. What are the chances that she will pass on a disease-causing allele for this disorder? AO 8.75 C25 D. 50% E 100%
Question 24 This pedigree (Pedigree #2) illustrates the inheritance of a simple Mendelian trait. What is the genotype of individual I-17 Lo- O AAA B. Aa ос. аа ODA
This pedigree (Pedigree #1) illustrates the inheritance of a simple Mendelian disorder. What is the genotype of individual II-2? OAA B. MA OC. Aa D.aa
Question 20 This pedigree (Pedigree #1) illustrates the inheritance of a simple Mendelian disorder. What is the likely mode of inheritance A autosomal dominant B. autosomal recessive C. cannot be determined from the information given D. (This is not a choice.) A Moving to another question will save this response.
4. Assume that the trait in the accompanying pedigree is due to simple Mendelian inheritance. . Co to odno a) Is it likely to be due to a dominant allele or a recessive allele? Explain. b) What is the biological relationship between Ill1 and 1112 c) If the allele responsible for the condition is rare, what are the most likely genotypes of all the people in the pedigree in generations I, II and III? (Use A and a for the...
In simple Mendelian inheritance alleles display a simple dominant/recessive relationship. There are many exceptions to Mendelian laws of inheritance. Most genes have more than two allelic forms and do not exhibit simple Mendelian inheritance. The human ABO antigens are an example of a multiple allelic trait. There are three ABO blood group antigens, IA, IB and i. The i allele is recessive to both IA and IB. A person who is homozygous ii has type O blood and does not...
this is all that im given Question 3: (4 points) Consider the following pedigree: O O 1 2 3 4 5 Characterize each of the following modes of inheritance as: Impossible, Possible, or Most likely. Justify your answers. a. Autosomal dominant b. Autosomal recessive X-linked dominant d. X-linked recessive e. Y-linked f. Going with the most likely mode of inheritance .... Assume individual V-1 marries a phenotypically normal male. What is the likelihood that their first child is affected with...
93. The pedigree below shows the sex-linked recessive inheritance of Nance-Horan syndrome, a rare Mendelian disorder in which affected persons have cataracts and abnormally shaped teeth. What is the probability that the first child of IV-6 and V-3 would have Nance-Horan syndrome? Iv A) 114 B) 1/2 C) 1/8 D) 3/16 E) 3/4
The mode of inheritance for this pedigree is autosomal dominant. If I-1 and II-2 were to have another child, what is the probability that their child would express the trait? Explain. 1 1 N II 1 3 4 5 6 N = 1 2 3 4 5 6
Genetics and Heredity Practice Problems A. Mendelian Genetics 1. In humans, achondroplasia or "dwarfism (D) is dominant over normal (d). A homorygous dominant (DD) person dies before the age of one. A heterozygous (d) person is dwarfed. A homozygous recessive individual is normal. If a heterozygous dwarf man marries a dwarf heterozyrous woman a. What is the probability of having a normal child? b. What is the probability of having a child that is a dwarf? What is the probability...