Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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The pedigree below represents what mode of inheritance?
Question 27 options:
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Y-linked dominant |
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X-linked recessive |
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Y-linked recessive |
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autosomal dominant |
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X-linked dominant |
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- 70 T 꿈 ㅁ ㅁ 이어어어어어어 In the pedigree shown, indicate whether each of the following inheritance patterns is possible by selecting YES or NO from the appropriate drop down menu. Y-linked Autosomal Recessive Autosomal Dominant X-linked Recessive X-linked Dominant ()arrow_forwardPLEASE tell me what each pedigree diagram is. so which one is most likely to show a family with Haemophilia A? most likely to show a family with Gaucher Disease? most likely to show a family with Sickle Cell Anaemia? most likely to show a family with Achondroplasia? most likely to show a family with Goltz Syndrome? What is the most likely inheritance pattern shown in image B, below?arrow_forwardY-linked ㅁㅇ O ㅇㅁ In the pedigree shown, indicate whether each of the following inheritance patterns is possible by selecting YES or NO from the appropriate drop down menu. Autosomal Recessive Autosomal Dominant X-linked Recessive X-linked Dominant ◆ 마음 (>> 01arrow_forward
- Tell me whether it is autosomal reccessive inheritance,autosomal domiant inheritance,sex-linked reccessive inheritance, sex-linked dominay inheritance or y-linked inheritance.arrow_forwardUse the following information to answer the next question. Pedigree Demonstrating the Inheritance of an Autosomal Recessive Trait GOO What is the most likely genotype of individual 1-1 in the pedigree above? Select one: OA Homozygous dominant OB. Heterozygous OC Homozygous recessive OD. Can be either homozygous dominant or heterozygousarrow_forwardthe pedigree below shows the inheritance of a newly identified eye color gene. Assume 100% penetrance and expressivity. Use the pedigree to find: 1. Identify the mode of inheritance (either autosomal dominant, or autosomal recessive) 2. Argue why your mode of inheritance must be correct. Your argument should cite specific individuals from the pedigree. (For example, the top left individual is person I-1).arrow_forward
- QUESTION 22 Consider whether the mode of inheritance for each of the pedigrees below is autosomal dominant or autosomal recessive Pedigree I Both pedigrees show autosomal dominant modes of inheritance Pedigree I is autosomal dominant while pedigree II is autosomal recessive O Pedigree I is autosomal recessive while pedigree II is autosomal dominant O Both pedigrees show autosomal recessive modes of inheritance QUESTION 23 A Pedigree II The pedigree below shows the inheritance of an X-linked recessive disorder. B TH Quersarrow_forwardExamine the pedigree and answer the following questions; shaded individuals show the trait; genotypes are all unknown. The individual marked with the question mark is of an unknown genotype but does have the trait. A. What mode of inheritance is the most likely for this trait, autosomal recessive or autosomal dominant? State your rationale for full credit. B. What is the genotype of the individual marked with the question mark? (Heterozygous, homozygous, or unknown)arrow_forwardCan you please not type the answer can you write it on a paperarrow_forward
- Aa Aa Carrier Carrier aa Aa Aa AA Affected Carrier Carrier Normal 42. What inheritance pattern is illustrated in the following pedigree?arrow_forwardExamine the pedigree and answer the following questions; shaded individuals show the trait; genotypes are all unknown. The individual marked with the question mark is of an unknown genotype but lacks the trait. A. What mode of inheritance is the most likely, autosomal recessive or autosomal dominant? State your rationale for full credit. B. What is the genotype of the individual designated with the question mark? (Heterozygous, homozygous, or unknown). C. What are the genotypes of the parents in generation I? (Heterozygous, homozygous, or unknown). D. What are the genotypes of the three children of generation IV? (Heterozygous, homozygous, or unknown).arrow_forward
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