11.32 For the pedigrees A and B, indicate whether thetrait involved in each case could be recessive or domi-nant, and explain your answers.GenerationIIIPedigree A121 2 34III1 23 4Pedigree BGenerationI12IIIII1 2 3 45671 23

Answered: Image /qna-images/answer/03678301-ff09-4e63-bfb8-d890c262c35b.jpg

Answered: 11.32 For the pedigrees A and B,…

Human Anatomy & Physiology (11th Edition)

11th Edition

ISBN:9780134580999

Author:Elaine N. Marieb, Katja N. Hoehn

Publisher:Elaine N. Marieb, Katja N. Hoehn

Chapter1: The Human Body: An Orientation

Section: Chapter Questions

Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...

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Similar questions

Alberta is phenotypically normal, but her brother (Rodrigo) has albinism, which is caused by an autosomal recessive mutation. The probability that Alberta is a carrier (i.e., heterozygous for albinism) is [express your answer as a fraction]
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The following pedigree represent a disease that is very rare in the human population and completely penetrant. What is the mode of inheritance? What is the probability that a child indicated with an "A" will inherit the disease? SHOW YOUR WORK. A? Enr the toolhar prees Al T+F10 (PC)gr ALT+EN+F10 (Mar)
the 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).
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 Quers
this is for primer 2 not primer 1
58 A family has two children with an undiagnosed, very rare neurodevelopmental condition illustrated in the pedigree below. Neither parent is affected and there is no family history of this disorder. The following two questions relate to this pedigree. What is the most likely mode of inheritance for this condition? Select one alternative: Dominant O It is not inherited Recessive X-linked recessive
The Pedigree shown is O O 마ㅇ ㅇㅇㅇ 이탕 - ㅁㅁㅇㅁ 5 A) Autosomal Dominant B) Sex linked recessive C) Autosomal Recessive D) Sex linked dominant
A rare blinding disease that has a relation to dengenerative factors is partially penetrant. In the following pedigrees for two families, the affected symptomatic individuals (black circles and squares) have been diagnosed with this disease due to the mutation in mitochondrial DNA m.14484T>C. If III.4 is homoplasmic for m.14484T>C in hair, blood, urine and other tissues examined. What will occur with IV.7 then?
Analyze the karyotype shown. Indicate if it is a chromosomal male or achromosomal female. If the karyotype is normal, write the word normal under name or description. If the karyotype is abnormal, name or describethe disorder.

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11.32 For the pedigrees A and B, indicate whether the trait involved in each case could be recessive or domi- nant, and explain your answers. Generation I II Pedigree A 1 2 1 2 3 4 III 1 2 3 4 Pedigree B Generation I 1 2 II III 1 2 3 4567 1 2 3