In this case a family history revealed a genetic basis for the disorder. The pedigree is shown in Fig. 1 Below.KeyØFemale: affectedFemale: unaffectedI||IVVTOLO5DO머910a. Any of these options is possibleb. III.5 but not V.3 would display the diseaseO c.V.3 but not III.5 would display the diseaseO d. Neither III.5 nor V.3 would display the diseaseOe. Both III.3 and V.3 would display the disease10નMale: affectedMale: unaffectedDeceasedDisease status not givenDizygotic twinsMonozygotic twinsFig. 1 Disease pedigree. Five generations I, II, III, IV, V are shown. Females are represented by circles, males by squares, dizygotic (non-identical) twins bydiagonal lines originating from the same point, Monozygotic (identical) twins by diagonal lines originating from the same point and joined symbols and deceasedby a diagonal line through the symbol. Filled symbols indicate that the individual displays the disease phenotype. Unfilled symbols indicate that the individualdoes not display the disease phenotype. Carriers of the disease are not indicated. Information on disease status is not known for generation I and is omitted forthe individuals represented by a symbol with an asterisk. The person referred to in the opening paragraph above is V.1. Consider which pattern(s) of Mendelianinheritance is (are) suggested by this pedigree and then answer questions 4-6Question 5) The disease status of individuals III.5, V.3 is not given in Fig. 1. Considering the pedigree and your deduced mode of inheritance which of thefollowing would you expect

Name: In this case a family history revealed a genetic basis for the disord
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Description: In this case a family history revealed a genetic basis for the disorder. The pedigree is shown in Fig. 1 Below.KeyØFemale: affectedFemale: unaffectedI||IVVTOLO5DO머910a. Any of these options is possibleb. III.5 but not V.3 would display the diseaseO